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Article

A Comprehensive Analysis of CSN1S2 I and II Transcripts Reveals Significant Genetic Diversity and Allele-Specific Exon Skipping in Ragusana and Amiatina Donkeys

by
Gianfranco Cosenza
1,* and
Alfredo Pauciullo
2,3,*
1
Department of Agriculture, University of Naples Federico II, 80055 Portici, NA, Italy
2
Department of Agricultural, Forest and Food Sciences, University of Turin, 10095 Grugliasco, TO, Italy
3
National Research Council of Italy, Institute of Animal Production in the Mediterranean Environment, Piazzale Enrico Fermi 1, 80055 Portici, NA, Italy
*
Authors to whom correspondence should be addressed.
Animals 2024, 14(20), 2918; https://doi.org/10.3390/ani14202918
Submission received: 12 September 2024 / Revised: 3 October 2024 / Accepted: 8 October 2024 / Published: 10 October 2024
(This article belongs to the Section Animal Genetics and Genomics)
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Abstract

:

Simple Summary

In recent decades, interest in the use of donkey milk for human nutrition has increased, since it may represent a natural substitute for cow’s milk for children affected by milk protein allergies. The functional peculiarities of donkey milk are mainly linked to its casein content comparable to that of human milk. This study provides a thorough analysis of transcript isoforms generated by two αs2-casein-encoding genes (CSN1S2 I and CSN1S2 II) in donkeys and a detection of significant genetic diversity at both loci along with sequence comparisons across species. In particular, a key mutation affecting exon 17 splicing in CSN1S2 I was identified, and a genotyping method was developed. These data represent an important step in the understanding of the expression regulation of these genes in donkeys and a useful tool for the genetic improvement of donkey milk production that fulfils special consumer requirements.

Abstract

The αs2-casein is a phosphoprotein secreted in the milk of most mammals, and it is the most hydrophilic of all caseins. Contrary to genes found in ruminants, in donkeys two different encoding genes for donkey αs2-casein (CSN1S2 I and CSN1S2 II) have been identified. However, unlike in ruminants, the variability at these loci has not been characterized in detail in donkeys until now. In this study, we analyze the transcript profile of the donkey CSN1S2 I and CSN1S2 II genes, and we identify and describe the variability of these loci in the Ragusana and Amiatina breeds reared in Italy. The analysis of the CSN1S2 I Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) products and subsequent sequencing showed, in addition to correctly spliced mRNA, seven other minor mRNAs resulting from differential splicing events involving, in various combinations, entire exons (4, 5, 6, and 11), parts of exons (5′ or 3′ end of exon 17), or the recognition of intronic sequences as an exon (exon 12′). Similarly, the transcription analysis of the CSN1S2 II gene revealed a remarkable variability in splicing events, mainly concerning the alternative insertion of an extra exon 7 (named 7′); the first 33 bp of exon 13; or the alternative skipping of exons 9, 10, 11, 12, and 15, and their combinations. At the mRNA level for CSN1S2 I, seven SNPs were observed, five of which led to amino acid changes: p.T73>A, p.I109>V, p.I130>V, p.I146>T, and p.D217>Y. Similarly, nine SNPs were observed at the CSN1S2 II locus, seven of which are non-synonymous: p.L63>F, p.H70>Q, p.D90>N, p.129A>T, p.H131>Y, p.E144>G, and p.F157>S. In addition, the DNA sequencing of exon 17 and flanking introns of the CSN1S2 I gene revealed a G>A transition at the splice acceptor site of CSN1S2 I exon 17 (FM946022.1:c.375-1G>A), resulting in an allele-specific skipping of the first 15 nucleotides of this exon, which encode the peptide 176NKINQ180, and the recognition of an in-frame cryptic splicing acceptor site: arAACAAAATCAACCAG. A genotyping method based on restriction fragment length polymorphism (XbaI PCR-RFLP) was set up for this SNP. In the total population studied (105 Ragusana and 14 Amiatina donkeys), the A allele had a frequency of 0.2437 with no evidence of deviation from the Hardy–Weinberg equilibrium. This study adds new knowledge regarding the genetic variability of αs2-caseins in donkeys and may contribute significantly to the genetic improvement of milk production for this species.

1. Introduction

The domestic donkey (Equus asinus) is a quadrupedal mammal belonging to the order of odd-toed ungulates (Perissodactyla) and sub-order of horse-like (Hippomorpha). It is part of the horse family (Equidae), which also includes the horse (Equus caballus) and the zebra (Equus zebra). This family includes the genus horse (Equus).
Although the donkey species continues to maintain great importance in many developing countries, technological evolution, the economic development of many rural areas, and the spread of agricultural machinery are making this animal increasingly less useful to its traditional “employer”. Consequently, especially in industrialized countries like Italy, it increasingly risks the fate of its wild ancestors. In the 1950s, there were almost a million donkeys in Italy, but their population has drastically decreased over time. It was only in 2000 that a rapid recovery began, saving many autochthonous breeds such as the Asinara, Pantesco, Grigio Siciliano, Romagnolo, Amiatina, Sardo Grigio, Martina Franca, and Ragusana [1,2] from extinction. One reason for this is the growing interest in the use of donkey milk for human nutrition, leading to this species now being considered a minor dairy species. Different studies have been performed to evaluate the safety of donkey milk in patients allergic to cow’s milk. The results of these studies were consistent, showing that more than 80% of the examined cow’s milk allergic patients tolerated donkey milk after an oral food challenge [3]. In addition, donkey milk is efficient in releasing anti-inflammatory interleukins, upregulating the immune response in aged hosts, preventing atherosclerosis, and acting as an anti-proliferative and anti-tumor agent [4]. Furthermore, the parapharmaceutical and cosmetic industries are particularly interested in formulating products based on donkey milk [5], whose therapeutic and aesthetic properties have been known since ancient times.
The functional peculiarities of donkey milk are mainly linked to its protein content. In fact, donkey milk is characterized by a lower content of caseins and whey proteins compared to ruminants’ milk, and its quantity of casein is comparable to that of human milk. In particular, the average content of caseins (34.61%) and whey proteins (49.80%), with a casein to whey protein ratio of 0.69, shows remarkable differences in comparison with bovine and other ruminant milks. The casein fraction in donkey milk (5.12 mg/mL) is mainly represented by αs1-CN (1.82 mg/mL) and β-CN (2.77 mg/mL), as well as smaller amounts of αs2-CN (3.68 × 10−1) and κ-CN (1.42 × 10−1) [6].
However, despite the growing interest in this species and its production, studies on the quantitative and qualitative aspects of donkey milk production are still limited compared to those conducted on the milk of other species, such as ruminants of zootechnical interest. Only recently have several studies been carried out to characterize its protein components and the genetic variability of the main genes coding for the different casein and whey protein fractions [6,7,8,9,10,11,12,13,14,15].
The proteomic approach has allowed characterization of the casein compositional heterogeneity due to post-translational modifications, like phosphorylation (αs1, αs2, and β-CN) and glycosylation (κ-CN) [7,8].
In particular, αs2-CN shows great heterogeneity due to variable degrees of phosphorylation [7,8,16,17]. The complex polymorphism of donkey αs2-CN is also characterized by the identification of two different CSN1S2 genes, called CSN1S2 I and CSN1S2 II, so far characterized only at the cDNA level. The first, spanning over a fragment of 1016 bp, is constituted by 19 exons, and it encodes for a protein of 221 amino acids (called αs2-CN-I); on the other hand, the second is constituted by 16 exons and probably originated by gene duplication [12]. Both genes, similarly to the equine species, are closely associated and map on chromosome 3 (gene IDs 106835119 and 106828076, respectively, for CSN1S2 I and CSN1S2 II, https://www.ncbi.nlm.nih.gov/gene/ accessed on 9 October 2024). Contrary to what happens in humans, but similar to rabbit, the CSN1S2 II gene seems to be functional in donkeys, leading to the effective translation of mRNA into the αs2-CN-II protein [7].
Of the two genes, the one that has been relatively more investigated is CSN1S2 I, characterized at the transcript and/or proteomic level in Ragusana breed donkeys [6,12,16,17]. More recently, both genes have been characterized using a combination of molecular biology (cDNA sequencing) and proteomic tools in the Amiatina breed [7].
The research conducted by these authors highlights significant genetic variability and the existence of different αs2-CN splicing isoforms, although the results are not always directly comparable, likely due to the two different breeds investigated.
Therefore, the primary aim of the present study was to comprehensively characterize the transcripts of the CSN1S2 I and CSN1S2 II genes in the Ragusana breed, analyze splicing and skipping events, investigate the genetic diversity of these two genes, and propose an evolutionary phylogenetic analysis to understand CSN1S2 gene differentiation among representative species of the orders Perissodactyla, Cetartiodactyla, and Carnivora. The Amiatina donkey has been used as a comparison breed.

2. Materials and Methods

2.1. Donkey Breeds

The Ragusana donkey, a native Sicilian breed from southern Italy, is one of the most productive breeds reared in Italy. It is used for recreational activities, trekking, and onotherapy, as well as for its notable milk production. In fact, with an average daily milk yield of 1.64 kg, it is more productive than other Italian breeds such as Amiatina and Martina Franca [18].
The Amiatina donkey is an endangered breed from Tuscany (central Italy), with additional animal units in Liguria and in southern Italy (Campania region). Historically, this breed was used as a pack animal on farms and in mines. Today, it is used for trekking, onotherapy, and milk production with an average daily milk yield of 0.7 kg [18,19].

2.2. mRNA Samples

For this study, 8 unrelated female donkeys of the Ragusana breed were used. They were of comparable age (approximately 6 years old); fed the same type of feed (hay and concentrate); and were at similar diet, feeding level, and lactation stage (about 60 days). The donkeys were kept in individual indoor stalls and reared on the same breeding farm located in southern Italy. Total RNA was extracted from somatic cells present in the milk using Nucleospin® RNA Plus XS (Macherey-Nagel, Düren, Germany). All milk samples used for the analyses were collected by authorized personnel during the periodic veterinary control.

2.3. DNA Samples

All the samples used in this study were obtained from previous research and are part of collections of the University of Torino (northern Italy) and University of Naples (southern Italy). Specifically, 105 DNA samples were originally isolated from individual blood samples of Ragusana donkeys, and 14 samples were from Amiatina donkeys, reared in different Italian regions. These individual blood samples were collected during routine prophylaxis by official veterinarians from the Local Sanitary Units (ASLs) of the Ministry of Health. Therefore, approval from the Animal Care and Use Committee was not necessary.

2.4. Primer Design, RT-PCR Conditions for Amplification, and Cloning of the Donkey CSN1S2 I and CSN1S2 II cDNAs

Primer pairs, purchased from Eurofins (Eurofins Genomics, Ebersberg, Germany), were designed using published Equus asinus nucleotide (cDNA) sequences (Supplementary Material, Table S1).
Reverse transcriptions (RTs) for the amplification of the cDNA of the donkey CSN1S2 I and CSN1S2 II genes were performed by using the ImProm-II™ Reverse Transcriptase and oligo dT for priming, following the manufacturer’s instruction protocol (Promega, Madison, WI, USA).
The 100 μL PCR reaction mix for the amplification of both cDNAs comprised 20 μL of RT reaction product; 50 mM KCl; 10 mM Tris–HCl (pH 9.0); 0.1% Triton X-100; 2 mM MgCl2; 10 pmoL of each primer, dNTPs each at 0.2 mM; and 5 U of Taq DNA Polymerase (Promega, Madison, WI, USA). The thermal profile of the PCR amplification consisted of 39 cycles: the first cycle involved a denaturation step at 97 °C for 2 min, an annealing step at 57 °C (for CSN1S2 I) or 50 °C (for CSN1S2 II) for 30 s, and an extension step at 72 °C for 1 min and 30 s. The next 37 cycles were performed under the following conditions: 94 °C for 30 s, 57 or 50 °C for 30 s, and 72 °C for 1 min and 30 s. In the 39th cycle, the extension step was carried out at 72 °C for 10 min.
The amplified products were first analysed by electrophoresis on a 2% agarose gel in TBE 0.5X buffer, stained with SYBR green nucleic acid stain (Lonza Rockland Inc., Rockland, ME, USA), and then cloned using the TOPO Cloning Reaction Kit (Invitrogen, Life Technologies Inc., Carlsbad, CA, USA), following the manufacturer’s instructions.

2.5. Screening of Clones by PCR and Sequencing

The screening of the clones was accomplished by PCR using the same forward and reverse primers used for the initial cDNA amplification. The reaction took place in 25 μL of mix, which included 0.5 μL of overnight fluid cultures of transformed cells, 50 mM KCl; 10 mM Tris–HCl (pH 9.0); 0.1% Triton X-100; 3 mM MgCl2; 5 pmol of each primer, dNTP 200 μM each; 2.5 U of Taq DNA Polymerase; and 0.04% BSA. The amplification program began with a cell lysis and nuclease inactivation step at 94 °C for 10 min. Subsequently, 30 reaction cycles were performed as indicated in the previous paragraph. Plasmids from positive colonies were sequenced on both strands by Eurofins Genomics (Ebersberg, Germany).

2.6. Genomic DNA Sequencing

The donkey genome sequence (GenBank acc. no. JADWZW020000003.1, region: 152933458 to 152933994, chromosome 3) was used to design primers (Table S1) for PCR amplification and sequencing of the DNA region spanning exon 17 and the 3′-flanking regions of the CSN1S2 I gene.
The reaction mix volume was 25 μL and was composed of 100 ng of genomic DNA; a 1X Green GoTag Flexi Buffer; 1.5 mM of MgCl2; 200 μM of each dNTP, 10 pmol of each primer; and 1 U of GoTaq® G2 Flexi DNA Polymerase (Promega, Madison, WI, USA).
The amplification programs consisted of 31 cycles. The first cycle was characterized by denaturation at 97 °C for 2 min, annealing at 54.5 °C for 45 s, and an extension step at 72 °C for 1 min. The next 30 cycles involved denaturation at 94 °C for 45 s, annealing at 54.5 °C for 45 s, and extension at 72 °C for 1 min, with the exception that in the last cycle the extension time was prolonged to 10 min. All amplicons were sequenced on both strands by Eurofins Genomics (Ebersberg, Germany).
For the genomic sequencing of the donkey CSN1S2 I gene, we selected 16 test samples: the same 8 Ragusana subjects used for transcript analysis plus 8 randomly chosen Amiatina donkeys.

2.7. Genotyping of Donkey at CSN1S2 I Locus by XbaI PCR-RFLP

A genotyping method based on PCR-RFLP (Restriction Fragment Length Polymorphism) was developed to screen the FM946022.1: c.375-1G>A transition at the splice acceptor site of the donkey CSN1S2 I exon 17 in the population.
The DNA fragment of 558 bp was amplified using the primers, reaction mix, and thermal conditions described above for genomic DNA sequencing.
Digestion of 6 μL of each PCR amplification was performed with 10 U of XbaI endonuclease (Promega, Madison, WI, USA) for 5 h at 37 °C, following the supplier’s directions for buffer conditions. PCR and digestion products were analysed directly on 3% agarose gels in TBE buffer 0.5X and stained with SYBR green nucleic acid stain (Lonza Rockland Inc., Rockland, ME, USA).
The entire panel of 119 donkey DNA samples was genotyped.

2.8. Bioinformatics and Statistical Analysis

Allele frequencies were calculated by simple allele counting. Possible deviations of genotypic frequencies from expectations were tested by a chi-square test to verify if the population was in the Hardy–Weinberg equilibrium. Homology searches, comparisons among nucleotide and amino acid sequences, and multiple alignments were accomplished using Dnasis Pro 3.0 (Hitachi Software Engineering Co., Tokyo, Japan).

3. Results and Discussion

3.1. Analysis of the Transcripts

3.1.1. CSN1S2 I

Amplicons obtained by the retro-transcription of eight donkey mRNA samples were cloned, screened, and sequenced.
The analysis of the cloned RT-PCR fragments of the CSN1S2 I gene was performed on a total of 160 positive clones (about 20 per sample). Sequencing results of 80 randomly chosen clones (10 per sample) showed the presence of at least 8 cDNA populations (Table 1; Figure 1).
The most represented population was that correctly assembled encoding for a full-length donkey αs2-CN I of 221 amino acids. According to Cosenza et al. [12], this cDNA is composed of 19 exons, ranging in size from 24 bp (exons 4, 8, and 15) to over 100 bp (exon 19). The signal peptide (MKFFIFTCLLAVALA) is coded from the 12th to the 56th nucleotide of the exon 2, while the stop codon (TAA) is located at the 10th–12th nucleotide of the exon 18.
The remaining seven transcripts are the results of differential splicing events involving, in various combinations, entire exons (4, 5, 6, and 11) or parts of exons (5′ or 3′ end of the 17th exon), or the recognition of intronic sequences as an exon (exon 12′) (Table 1; Figure 1).
In detail, the alternative skipping of the first 15 nucleotides of exon 17 (AACAAAATCAACCAG, Supplemental Figure S1) is responsible for the deletion of the pentapeptide 176NKINQ180, which appears to be constitutively spliced in the αs2-CN from mares [17].
This seems to be due to a G>A transition that alters the canonical splice acceptor site in equine species, leading to the recognition of a second in-, frame splice acceptor site (nucleotides 14–15) [7]. We observed the alternative skipping of the first 15 nucleotides of exon 17 either alone or in conjunction with the simultaneous skipping of exons 4, 5 and 6, similarly to what has been reported by Saletti et al. [17] and Cunsolo et al. [16] in the same breed. The first 15 bp of exon 17 are a perfect duplication of the first 15 nucleotides of exon 12 (coding for the pentapeptide 92NKINQ96). It is likely that exon 12 and exon 17, both 129 bp in length, are at least partially the result of an internal duplication, similar to that of exons 11 and 16 (Supplemental Figure S2).
Exon duplication is a common event in the evolution of the CSN1S2 and CSN1S1 genes. The presence of many small exons of similar size suggests that duplication events have contributed to the exon structure of these genes in mammals [20].
For example, in donkey CSN1S2 I, exons 8 and 10, along with the flanking regions, are perfectly duplicated (Supplemental Figure S2). A similar duplication event was observed also in Old-World Camels’ CSN1S2 cDNA where exons 8 and 11 shared 22 and 17 out of 24 bp (ESAEVTPE and ESTEVTPE). These two exons in camels corresponded to exon 9 in the cattle CSN1S2 sequence, where no such duplication occurred [21].
Similarly, duplications of exons or the recognition of introns as coding sequences also characterize the CSN1S2 gene in bovids [20,22]. A second event involves exon 17 and the alternative skipping of its 3′ extremity (35 nucleotides) (Supplemental Figure S3) either together with or independent of the concurrent absence of exons 4, 5, and 6 (Figure 1; Table 1).
The deletion observed at the 3′ end of exon 17 reveals a cryptic splice site (casual usage of cryptic splice sites), disrupting the coding triplet of the αs2-casein reading frame and causing a frameshift of the termination codon (TAA), which is normally established with the third codon of exon 18, now changed to a TAA stop codon 26 nucleotide downstream in exon 18. Such an event would lead to the translation of a sequence of the exon 18, which is normally only transcribed. As a consequence, this mRNA retains an open reading frame despite the frameshift and would translate an αs2 lacking the peptide 207SKTNSYQIIPVLRYF221 but with a new C-terminal sequence: 207KVLLRFLN214 (Figure 1).
Transcripts characterized by this event in the donkey species were also observed by Saletti et al. [17], Cunsolo et al. [16], and Auzino et al. [7]. However, Saletti et al. [17] and Cunsolo et al. [16] reported only the deletion of the peptide YQIIPVL.
A similar event was also observed at the 3′ end of the exon 15 of the CSN1S2 gene in camelids (corresponding to exon 17 in donkeys), where an isoform results from an alternative splicing event of the decapeptide VKAYQIIPNL due to the identification of a cryptic splice site, although the reading frame is not altered (Supplemental Figure S3) [21,23].
Finally, transcripts have been observed that are characterized by the presence of an extra exon of 105 nucleotides, which, being skipped between exons 12 and 13, is numbered as 12′ (Figure 1). This is likely an intronic sequence that is occasionally recognized as an exon.
The sequence of this extra exon, 12′, and its flanking regions, i.e., the splicing sites, is perfectly conserved also in the horse and zebra CSN1S2 I gene (Supplemental Figure S4). Thus, it is very likely that a small proportion of the mRNAs in these species also contain this exon.
Due to the presence of a TAA codon between nucleotides 28 and 30 of the extra exon, this transcript is expected to translate into a 143 amino acid protein ending with the nonapeptide EGIEIIIFM. However, since this is a premature translation termination, it may lead to rapid mRNA degradation by nucleases, resulting in a low level of such messengers in the cytoplasm. This process, known as non-sense-mediated RNA decay (NMRD), has already been described in goats for other casein-encoding genes, such as CSN2, CSN1S1, and CSN1S2 [24,25,26].
Finally, the alternative skipping of exons 4, 5, and 6 observed in the present study was also reported by Cunsolo et al. [16] and Auzino et al. [7] (Table 1) and should therefore be considered constitutive, allele-independent events that occur during the maturation of the pre-mRNA of the donkey CSN1S2 I gene.

3.1.2. CSN1S2 II

The screening of 160 positive clones (20 from each sample) of the CSN1S2 II gene and the subsequent sequencing of about 60 randomly chosen clones revealed at least nine different populations of mRNA. The most represented population corresponds to a correctly assembled transcript encoding a mature donkey αs2-CN II of 142 amino acids. The remaining transcripts are characterized by the alternative skipping of individual exons (7′, 9, 10, or 15) or the simultaneous skipping of exons 9, 10, and 15; exons 11, 12, and the first 33 bp of exon 13; exons 11, 12, the first 33 bp of exon 13, and exon 15; or exon 9 with the presence of exon 7′ (Table 2, Figure 2).
According to Cosenza et al. [12], the correctly assembled mRNA consists of 16 exons, with sizes ranging from 24 bp (exons 7, 9, and 11) to over 200 bp (exon 16). The signal peptide (MKFFIITCLLAVALA) is coded from the 13th to the 57th nt of exon 2, while the stop codon (TAA) is located at the 10th–12th nucleotide of exon 14.
Interestingly, the AAACAGTTG duplication, which encodes the KQL tripeptide at the beginning of exon 13 as previously reported by Cosenza et al. [12], was not detected in any of the CSN1S2 II mRNAs sequenced. Therefore, it is reasonable to assume that this duplication should be considered an artifact, similarly to what has been observed by Auzino et al. [7].
Compared to the CSN1S2 I gene, the CSN1S2 II gene has been less thoroughly investigated in donkeys and other species. Since its identification by Cosenza et al. [12] in Ragusana breed donkeys, its characterization has recently been carried out by Auzino et al. [7] only in Amiatina breed donkeys.
When comparing the results of the present work with those reported by these authors, significant differences in the variability of alternative splicing are evident. In particular, in all the CSN1S2 II cDNA sequences analysed in the study by Auzino et al. [7], exons 3 and 7′ are constitutively missing and present, respectively (Table 2).
In contrast, none of the mRNA populations we observed are characterized by the skipping of exon 3, which encodes the 3EIKHVSSSE11 peptide, while the skipping of exon 7′, which encodes the KIELTKEEKLYLKQL (p.Asp50_Glu51ins15), is observed in only two of the detected transcript populations (Table 2). As reported by Auzino et al. [7], this exon appears to be nearly perfectly duplicated as exon 12, which encodes the peptide 85EIELSDEEKNYLKQL99 (Supplemental Figure S5). This exon is also involved in alternative skipping, further confirming that the phenomenon of coding sequences duplications observed in CSN1S2 I is also present in CSN1S2 II.
Alternatively, the sequence of the exon 7′ could be considered an “exonification” of an intronic region following the recognition of splice acceptor and donor sites. It is interesting to note that this intron has a triplet structure (45 bp), and its insertion does not alter the original reading frame, so the same primary amino acid sequence upstream and downstream of the insertion is maintained.
Alternative skipping observed in the present study, but not reported by Auzino et al. [7], involves exon 10 (encoding the KTSKKTVDM peptide) and exon 15 (105 bp) (Supplemental Figure S6). The latter is a non-coding exon (3′ UTR) and is therefore not responsible for variations in translation. Similarly to what was observed for exon 7′ at this locus or for exon 12′ at the CSN1S2 I locus, it is likely that an intronic region is recognized as an exon during the splicing process of the primary transcript. Since the sequence of exon 15 and its splicing sites are perfectly conserved in CSN1S2 II across Equus asinus, caballus, quagga, and przewalskii, it is very likely that a proportion of the mRNAs in these species may also contain this exon (Supplemental Figure S6).
It is plausible to hypothesize that the presence/absence of exon 15 could influence mRNA stability. Different studies have shown that 3′ UTRs are highly polymorphic in length and that a single gene can express multiple 3′ UTRs that differ in length, sequence, and assembly of regulatory motifs. It is known that the 3′ UTRs contain cis-regulatory elements recognized by trans-acting factors, and thus, changes in 3′ UTR length could alter several regulatory elements. In fact, many genes have an alternative 3′ UTR or contain internal introns that can switch 3′ UTR length. Therefore, changes in 3′ UTR length could affect gene expression by fine-tuning and reprogramming the mRNA regulatory landscape in cells [27,28].
In addition, similarly to what has been observed at exon 17 of CSN1S2 I, exon 13 of the CSN1S2 II gene is subject to the use of in-frame cryptic splice sites, leading to an alternative skipping of the first 33 nucleotides of exon 13 (GTGAAAATCAACCCAAAGTTCCCCTCTCCCCAG), which encodes the peptide 100VKINPKFPSPQ110 (Figure 2). We have never observed the alternative skipping of the first 33 nucleotides of exon 13 alone; it always occurs in conjunction with the simultaneous skipping of exons 11, 12, and/or 15, similar to what was reported by Auzino et al. [7] for the Amiatina breed (Table 2). A comparison of the sequences deposited in GeneBank shows that the presence of the cryptic splice sites at the 5′ of exon 13 is conserved among the different equid species (Supplemental Figure S7).
Concerning this event, the elimination of three nucleotides or those consisting of multiples of three from the mRNA, due to the recognition of a cryptic site of splice as an alternative to the canonical site (AG), is a feature common to the other casein-encoding genes. In particular, this event appears to be quite frequent in αs1-CN transcripts across various species, including sheep [29], cattle and buffalo [30], horse [31], goat [25], and humans [32].
Multiple forms of transcripts resulting from alternative splicing have also been demonstrated for αs2-CN in sheep [33,34], goats [35], buffalo [36,37], cattle [38], camels [21,23], and horses [39,40]. Similar defects in the processing of primary transcripts also characterize the αs1-CN gene (CSN1S1) in the same species [7,25,29,30,31,34,41,42,43,44,45], as well as in humans and pigs [33,46].
It has been proposed that exon skipping should be considered a frequent event when the coding region is divided into many short exons, as the maturation of long cognate primary transcripts appears to be an intricate process requiring many successive steps [34,47].
In general, alternative splicing resulting from the incorrect identification of donor or acceptor sites, leading to a shorter protein isoform compared to the full-length form or one characterised by premature stop codons, is a common event. This event has also been reported in other genes, such as DGAT 1 in cattle, yak, and buffalo [47].

3.2. Analysis of Genetic Diversity

3.2.1. CSN1S2 I and CSN1S2 II cDNA Polymorphisms Detection

The analysis and alignment of the cDNA sequences of the eight subjects used in this study have highlighted a remarkable genetic diversity at both loci investigated: CSN1S2 I and II.
At the CSN1S2 I locus, the comparison of the obtained sequence evidenced seven SNPs, comprising six transitions and one transversion, five of which were non-synonymous SNPs. In particular, four of these polymorphisms are located in exons 8, 10, 14, and 17, respectively, whereas the remaining ones are located in exon 12 (Table S2). Two of these polymorphisms s (a transition T>C at the 119th nucleotide of exon 12, responsible for the amino acid changes p.I146>T, and a silent G>A transition at the 12th nucleotide of exon 14) have already been reported by Cosenza et al. [12].
Similarly, the CSN1S2 II locus also seems to be characterized by notable polymorphisms. The comparison of the cDNA sequences revealed nine SNPs (eight transitions and one transversion), six of which resulted in putative amino acid exchange: p.L63>F, p.H70>Q, p.D90>N, p.A129>T, p.H131>Y, and p.E144>G (Table S3).
The non-synonymous SNP at the nucleotide 43 of exon 13 (p.A129>T) has already been observed by Auzino et al. [7], whereas the presence of the G in position 86 of exon 13, as reported in FN298386, was not observed in any of the analysed transcripts (Table S3).
The presence of such a high level of polymorphisms at the CSN1S2 locus is not unusual. In fact, studies of αs2-CN have revealed diverse protein and DNA polymorphisms across different species. In horses, a total of six non-synonymous single-nucleotide variants and one large deletion leading to eight distinct putative αs2-CN isoforms were identified [48]. Among ruminants, goats and sheep exhibit a higher level of genetic diversity at this locus, with at least eight and seven alleles characterized in the two species, respectively [26,35,49]. Similarly, eight alleles have been identified in buffalo, three of which are deleted alleles. These deleted alleles are characterized by the alteration of the acceptor splice site of exon 7, which leads to the skipping of this exon at the mRNA level [36]. Conversely, in cattle, only four variants have been characterized [50].
Recently, the characterization of the CSN1S2 gene has revealed genetic variations also in the Old-World Camels [21]. Such a high level of polymorphism is comparable only to those observed in the CSN1S1, CSN2, and CSN3 genes in goats [51,52] or CSN3 gene in cattle [53].
SNP detection through mRNA sequencing is particularly valuable for livestock species, as whole genome sequencing is expensive and exome sequencing tools are not available. Furthermore, SNPs detected in expressed regions can be useful for characterizing variants that affect protein function. However, data derived from RNA analyses are often considered a less-than-ideal source for SNP detection due to a higher false positive rate, which arises from both biological and technical factors. For example, RNA polymerases are known to commit errors through a process termed transcriptional mutagenesis. This process affects both mitotic and post-mitotic cells, as it is independent of DNA replication. Consequently, errors in transcription are generally considered transient, with no long-term consequences, and are not stably inherited from cell to cell. However, several lines of evidence now demonstrate that transcription errors are not always random or temporary, and that they can have lasting consequences, particularly in human health [54]. Technical factors contributing to errors include reverse transcription errors, which occur at a certain rate during the conversion of RNA to cDNA and are a mandatory step for RNA cloning, PCR amplification errors, and the error-prone nature of sequencing itself [55].
Therefore, to confirm the presence of the SNPs at donkey CSN1S2 I and II, uniquely identified through RNA cloning and sequencing, and to determinate their frequency, a future objective will be to sequence the exonic regions at DNA level or to carry out genotyping for these markers on a suitable number of donkeys belonging to the Ragusana breed.

3.2.2. DNA Sequences: Detection of a Point Mutation in the Splice Acceptor Site of CSN1S2 I Exon 17

As previously described, the screening of clones for the Ragusana CSN1S2 I gene and the subsequent sequencing revealed transcripts characterized by the alternative skipping of the first 15 nucleotides of exon 17. This results in an αs2-CN I isoform missing the pentapeptide 176NKINQ180. This event has been previously reported in the same breed by Saletti et al. [17] and Cunsolo et al. [16]. Conversely, Auzino et al. [7] did not observe any αs2-CN I isoforms lacking the pentapeptide 176NKINQ180 in the Amiatina breed.
It has therefore been hypothesized that the Ragusana breed, or more generally the donkey species, may be characterized by a polymorphism affecting the splice acceptor site of CSN1S2 I exon 17. In order to demonstrate this hypothesis, we sequenced exon 17 and flanking introns of the CSN1S2 I gene of eight Ragusana and eight Amiatina donkeys. The sequence comparison confirmed a point mutation (FM946022.1: c.375-1G>A) at the splice acceptor site of exon 17 in the Equus asinus CSN1S2 I gene in both breeds, resulting in allele-specific partial exon skipping (Supplemental Figure S8).
It is therefore possible to hypothesize that in donkeys homozygous for guanine (c.375-1G) the canonical splice site of exon 17 (long form) is recognized, while in donkeys homozygous for the adenine (c.375-1A) it would translate an αs2-CN isoform constitutively deleted of the 176NKINQ180 peptide (short form) similar to what has been reported for equine species.
It is interesting to note that the amino acid sequences NKINQ are traits of some IgE-binding epitopes of bovine αs2-CN. In particular, the NKINQ sequence is a trait of two major IgE-binding epitopes of bovine αs2-CN (Figure 3) and therefore could be related to the already demonstrated low allergenic properties of donkey’s milk [17].
The alteration of a splice acceptor/donor site, along with the resulting exon skipping, is an unusual event, although it has been observed in other species at this locus, such as in buffalo [36,37], or at other loci, like CSN1S1 in cattle [56] and sheep [43]. Therefore, similar to these examples, this case represents an intra-species allele-specific event, rather than a constitutive condition as reported for horses [17].

3.2.3. Genotyping of the SNP FM946022.1: c.375-1G>A in the Donkey CSN1S2 I Gene

The c.375-1G>A transition at the acceptor splice site of exon 17 of the CSN1S2 I gene alters a restriction site for the endonuclease XbaI (T/CTAGA). Consequently, a PCR-RFLP protocol was set up for the quick genotyping of samples. Digestion of the PCR product (558 bp) allows for the identification of both alleles. The restriction pattern is characterized by one undigested fragment in c.375-1A homozygous samples, whereas the same amplicon is restricted into two fragments of 187 and 371 bp in samples homozygous for c.375-1G. The restriction pattern of heterozygous samples shows all three fragments (Figure 4).
The genotype distributions and allelic frequencies of the polymorphism, determined in all 119 investigated donkeys (105 Ragusana and 14 Amiatina), are reported in Table S4.
Across the total investigated population, the G allele had a frequency of 0.7563, and the χ2 value (0.2818) indicated no significant deviation from the Hardy–Weinberg equilibrium (p ≤ 0.05).
It should be noted that among the 14 Amiatina donkeys, only two genotypes were observed: G/G (n = 9) and A/G (n = 5). Although the number of subjects investigated is limited, the allele and genotype frequencies are comparable to those observed in the Ragusana breed. Therefore, it is conceivable that the Amiatina donkeys studied by Auzino et al. [7] were homozygous for the c.375-1G allele, which could explain the absence of transcripts characterized by the skipping of the first 15 nucleotides of exon 17.
From the comparison of the sequences deposited in GeneBank, it is interesting to note that the presence of adenine, responsible for the skipping of the first 15 nt of the exon 17 at mRNA level, although present at low frequency in the donkey species (0.2437), appears to be a constitutive condition in all other species belonging to the different families within the Perissodactyla order: Equidae (horses and zebras) Rhinocerotidae (rhinoceroses), and Tapiridae (tapirs) (Supplemental Figure S9). Furthermore, all these perissodactyl species are characterized by the presence of a second splice acceptor site, which enables recognition of the exon 17 deletion of the first 15 nucleotides during the splicing mechanism (Supplemental Figure S9).
Among all the species belonging to the orders Cetartiodactyla or Carnivora, the simultaneous presence of both the canonical and cryptic acceptor sites of the 17th exon is observed only in those within the sub-order Ruminantia (Supplemental Figure S9). However, to date, no studies have reported a possible alternative skipping of the first 15 nucleotides of exon 17 at the CSN1S2 mRNA level in these species.
In general, it is possible that the G allele represents the ancestral condition of the CSN1S2 gene, as it is present in all species within the orders Cetartiodactyla and Carnivora for which sequences are available in GeneBank (Supplemental Figure S9). During the evolution of Perissodactyla, a G>A transition may have occurred, leading to the fixation of adenine in all families of this order, with the exception of the donkey species. Investigations are currently underway to assess whether this locus is also polymorphic in the remaining perissodactyl species, which could indicate the presence of a Trans-Specific Polymorphism (TSP), similar to what has been reported for other Cetartiodactyla species, such as hormone-encoding genes in goats, sheep, and buffalo [57,58] or milk protein-encoding genes in camelids [59]. TSPs are ancient genetic variants whose origin predates speciation events, resulting in shared alleles among evolutionarily related species [60]. Therefore, considering these observations, the G>A transition at the splice acceptor site of exon 17, in addition to being responsible for modifying the splicing mechanism and, consequently, associated with the regulation of donkey CSN1S2 I gene expression, could serve as a valuable marker for inter- and intra-species phylogenetic analysis.
The question of the phylogenetic origin of species is indeed complex and is often debated. In particular, the evolutionary dynamics between the orders Cetartiodactyla and Perissodactyla are somewhat complicated. Most studies suggest that these two ungulate groups form a clade (Euungulata), while the groups Carnivora and Philidota form the clade Ferea. Furthermore, in many phylogenies, Ferea and Euungulata are grouped together within a larger clade called Ferungulata [61]. However, the issue remains a subject of ongoing debates.

4. Conclusions

This study provides a comprehensive analysis of the transcripts and genetic variability within the CSN1S2 I and II loci in the domestic Ragusana breed of donkeys. We have elucidated the genetic events responsible for the various transcripts and described alternative splicing events that contribute to the complex expression patterns of donkey αs2-CNs. However, it is also reasonable to hypothesize the existence of transcripts forms others than those reported in this study, which have not been detected so far due to their existing in undetectable amounts. Significant genetic diversity at both the loci has been found. One example is the FM946022.1: c.375-1G>A transition at the splice acceptor site of exon 17 that results in allele-specific partial exon skipping. The presence of A seems to be a constitutive feature of the other perissodactyl species, indicating a possible evolutionary shift from the ancestral G allele common in Cetartiodactyla and Carnivora. Further investigation is needed to explore the potential trans-specific nature of this polymorphism across different species and its implications for gene expression regulation. Finally, our findings underscore the importance of continued study of the genetic diversity of donkey breeds, both for species conservation and for improving the quality and safety of donkey milk for human consumption.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ani14202918/s1. Figure S1: Results of CSN1S2 I cDNA sequencing. Alternative skipping of the first 15 nucleotides of exon 17 (AACAAAATCAACCAG). The large arrows indicate the exons; Figure S2: Comparison of Equus asinus genomic sequences covering (A) exons 11 and 16 and the flanking regions of the CSN1S2 I gene (GeneBank JADWZW020000003.1 from 152928702 to 152928763 and from 152932720 to 152932781); (B) exons 12 and 17 and the flanking regions of the CSN1S2 I gene (GeneBank JADWZW020000003.1 from 152930146 to 152930310 and from 152933634 to 152933793); (C) exons 8 and 10 and the flanking regions of the CSN1S2 I gene (GeneBank JADWZW020000003.1 from 152928328 to 152928636 and from 152926989 to 152927297). Exon sequences are in uppercase and bold letters. Acceptor and donor splice sites are underlined. Dashes represent identical nucleotides in the upper lines. Conserved amino acids are shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi); Figure S3: (A) Results of the CSN1S2 I cDNA sequencing. Alternative skipping of the last 35 nucleotides of exon 17. The large arrows indicate exons. (B) Comparison of Camelus dromedarius (GeneBank OQ730239 from 12122 to 12280) and Equus asinus (GeneBank JADWZW020000003.1 from 152933627 to 152933786) genomic sequences covering exons 15 and 17 of the CSN1S2 I gene, along with the respective flanking regions. Exon sequences and amino acids are in uppercase and bold letters. Acceptor and donor splice sites are underlined and shaded. Dashes represent identical nucleotides to those in the upper lines. Conserved amino acids are also shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi); Figure S4: (A) Comparison of Equus asinus (GeneBank JADWZW020000003.1 from 152930069 to 152930978), Equus quagga (GeneBank JAKJSB010001568.1 from 100897185 to 100896302, complement), Equus caballus (GeneBank PJAA01000004.1 from 66588578 to 66587670), and Equus przewalskii (GeneBank ATBW01083582.1 from 4801 to 3893, complement) genomic sequences covering exons 12 to 13 of the CSN1S2 I gene and their flanking regions. Dashes represent identical nucleotides to those in the upper lines. Exon sequences and amino acids are in uppercase and bold letters, and an asterisk indicates the premature termination stop codon. Acceptor and donor splice sites are underlined and shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi). (B) Results of the CSN1S2 I cDNA sequencing. The large arrows indicate exons; Figure S5: (A) Comparison of Equus asinus exon 7′ and 12 sequences of the CSN1S2 II gene. Dashes represent identical nucleotides to those in the upper lines. Conserved amino acids are shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi). Results of CSN1S2 II cDNA sequencing without (B) and with (C) exon 7′ (in red) sequence. The large arrows indicate exons; Figure S6: Results of CSN1S2 II cDNA sequencing. (A) Alternative skipping of exon 10. (B) Alternative skipping of exon 15; the large arrows indicate exons. (C): Comparison of Equus asinus (GeneBank PSZQ01005937.1 from 24169059 to 24169178, complement), Equus quagga (GeneBank JAKJSB010001568.1 from 100955081 to 100954962, complement), Equus caballus (GeneBank PJAA01000004.1 from 66663354 to 66663473, complement), and Equus przewalskii (GeneBank ATBW01081756.1 from 33803 to 33922, complement) genomic sequences covering exon 15 and flanking regions of the CSN1S2 II gene. Exon sequences are in uppercase and bold letters. Acceptor and donor splice sites are underlined and shaded. Dashes represent identical nucleotides to those in the upper lines. Alignment was performed using DNAsis pro Software v2.0 (Hitachi); Figure S7: (A) Results of CSN1S2 II cDNA sequencing. Alternative skipping of exons 11 and 12 and of the first 33 nucleotides of exon 13. The large arrows indicate exons. (B) Comparison of Equus asinus (GeneBank PSZQ01005937.1 from 24166892 to 24167071), Equus caballus (GeneBank PJAA01000004.1 from 66661191 to 66661370), Equus quagga (GeneBank JAKJSB010001568.1 from 100957247 to 100957068, complement), and Equus przewalskii (GeneBank ATBW01081756.1 from 31501 to 31680) genomic sequences covering exon 13 and flanking regions of the CSN1S2 II gene. Exon sequences and amino acids are in uppercase and bold letters. Canonical acceptor and donor splice sites and cryptic acceptor sites are underlined and shaded. Dashes represent identical nucleotides to those in the upper lines. Alignment was performed using DNAsis pro Software v2.0 (Hitachi); Figure S8: Results of the DNA sequencing of exon 17 and flanking regions of the donkey CSN1S2 I gene. (A) A/A homozygous sample. (B) G/G homozygous sample. (C) heterozygous sample. The acceptor splice sites of exon 17 are underlined. Solid arrows indicate the SNP (transition FM946022.1:c.375-1G>A) located in the acceptor splice site; Figure S9: Comparison of genomic sequences covering exon 17 of the donkey CSN1S2 I gene and predicted amino acid sequences with corresponding sequences from representative species of the Perissodactyla, Cetartiodactyla, and Carnivora orders. Exon sequences are in uppercase and bold letters. Amino acid sequences are highlighted. Canonical and cryptic acceptor and donor splice sites are shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi); Table S1: Oligonucleotide primers used for the characterization of the donkey CSN1S2 I and CSN1S2 II cDNAs; Table S2: Detection of polymorphisms at CSN1S2 I locus in Ragusana donkeys and corresponding electropherograms; Table S3: Polymorphisms detected at CSN1S2 II cDNA in Ragusana donkeys, corresponding electropherograms, and comparison with counterpart sequences available in the literature and GeneBank; Table S4: Genotyping data and allele frequency of the FM946022.1:c.375-1G>A transition at the acceptor splice site of exon 17 in the CSN1S2 I gene in Ragusana and Amiatina donkeys.

Author Contributions

G.C. and A.P. conceived, designed, and performed the experiments. G.C. and A.P. analyzed the data. G.C. contributed reagents, materials, and analysis tools. G.C. and A.P. wrote and revised the article critically for important intellectual content. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the University of Turin, Ricerca locale ex 60%, Grant Number BIAD_RILO_23_01 (Incremento della resilienza delle produzioni zootecniche).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki. No animal was harmed physically during the whole experimental period. Sampling was carried out by official veterinarians from the Local Sanitary Units (ASLs) of the Ministry of Health during routine prophylaxis. Therefore, approval from the Animal Care and Use Committee was not necessary and no ethics statement was needed for this study.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors thank donkeys’ owner for providing milk samples.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Bordonaro, S.; Dimauro, C.; Criscione, A.; Marletta, D.; Macciotta, N.P.P. The mathematical modeling of the lactation curve for dairy traits of the donkey (Equus asinus). J. Dairy Sci. 2013, 96, 4005–4014. [Google Scholar] [CrossRef] [PubMed]
  2. Colli, L.; Perrotta, G.; Negrini, R.; Bomba, L.; Bigi, D.; Zambonelli, P.; Verini Supplizi, A.; Liotta, L.; Ajmone-Marsan, P. Detecting population structure and recent demographic history in endangered livestock breeds: The case of the Italian autochthonous donkeys. Anim. Genet. 2013, 44, 69–78. [Google Scholar] [CrossRef] [PubMed]
  3. Maryniak, N.Z.; Sancho, A.I.; Hansen, E.B.; Bøgh, K.L. Alternatives to cow’s milk-based infant formulas in the prevention and management of cow’s milk allergy. Foods 2022, 11, 926. [Google Scholar] [CrossRef] [PubMed]
  4. Faccia, M.; D’Alessandro, A.G.; Summer, A.; Hailu, Y. Milk products from minor dairy species: A review. Animals 2020, 10, 1260. [Google Scholar] [CrossRef]
  5. Kazimierska, K.; Kalinowska-Lis, U. Milk proteins—Their biological activities and use in cosmetics and dermatology. Molecules 2021, 26, 3253. [Google Scholar] [CrossRef]
  6. Cosenza, G.; Mauriello, R.; Garro, G.; Auzino, B.; Iannaccone, M.; Costanzo, A.; Chianese, L.; Pauciullo, A. Casein composition and differential translational efficiency of casein transcripts in donkey’s milk. J. Dairy Res. 2019, 86, 201–207. [Google Scholar] [CrossRef]
  7. Auzino, B.; Miranda, G.; Henry, C.; Krupova, Z.; Martini, M.; Salari, F.; Cosenza, G.; Ciampolini, R.; Martin, P. Top-Down proteomics based on LC-MS combined with cDNA sequencing to characterize multiple proteoforms of Amiata donkey milk proteins. Food Res. Int. 2022, 160, 111611. [Google Scholar] [CrossRef]
  8. Chianese, L.; Calabrese, M.G.; Ferranti, P.; Mauriello, R.; Garro, G.; De Simone, C.; Quarto, M.; Addeo, F.; Cosenza, G.; Ramunno, L. Proteomic characterization of donkey milk “caseome”. J. Chromatogr. A 2010, 1217, 4834–4840. [Google Scholar] [CrossRef] [PubMed]
  9. Chianese, L.; De Simone, C.; Ferranti, P.; Mauriello, R.; Costanzo, A.; Quarto, M.; Garro, G.; Picariello, G.; Mamone, G.; Ramunno, L. Occurrence of qualitative and quantitative polymorphism at donkey beta-Lactoglobulin II locus. Food Res. Int. 2013, 54, 1273–1279. [Google Scholar] [CrossRef]
  10. Cosenza, G.; Ciampolini, R.; Iannaccone, M.; Gallo, D.; Auzino, B.; Pauciullo, A. Sequence variation and detection of a functional promoter polymorphism in the lysozyme c-type gene from Ragusano and Grigio Siciliano donkeys. Anim. Genet. 2018, 49, 270–271. [Google Scholar] [CrossRef]
  11. Cosenza, G.; Patrice, M.; Garro, G.; Gallo, D.; Barbara, A.; Roberta, C.; Alfredo, P. A novel allelic donkey β-Lg I protein isoform generated by a non-AUG translation initiation codon is associated with a non-synonymous SNP. J. Dairy Sci. 2023, 106, 4158–4170. [Google Scholar] [CrossRef]
  12. Cosenza, G.; Pauciullo, A.; Annunziata, A.L.; Rando, A.; Chianese, L.; Marletta, D.; Iannolino, G.; Nicodemo, D.; Berardino, D.D.; Ramunno, L. Identification and characterization of the donkey CSN1S2 I and II cDNAs. Ital. J. Anim. Sci. 2010, 9, e40. [Google Scholar]
  13. Criscione, A.; Cunsolo, V.; Tumino, S.; Di Francesco, A.; Bordonaro, S.; Muccilli, V.; Saletti, R.; Marletta, D. Polymorphism at donkey β-lactoglobulin II locus: Identification and characterization of a new genetic variant with a very low expression. Amino Acids 2018, 50, 735–746. [Google Scholar] [CrossRef]
  14. Herrouin, M.; Mollé, D.; Fauquant, J.; Ballestra, F.; Maubois, J.-L.; Léonil, J. New genetic variants identified in donkey’s milk whey proteins. J. Protein Chem. 2000, 19, 105–116. [Google Scholar] [CrossRef]
  15. Özdil, F.; Bulut, H.; Işık, R. Genetic diversity of κ-casein (CSN3) and lactoferrin (LTF) genes in the endangered Turkish donkey (Equus asinus) populations. Arch. Anim. Breed. 2019, 62, 77–82. [Google Scholar] [CrossRef]
  16. Cunsolo, V.; Saletti, R.; Muccilli, V.; Gallina, S.; Di Francesco, A.; Foti, S. Proteins and bioactive peptides from donkey milk: The molecular basis for its reduced allergenic properties. Food Research International 2017, 99, 41–57. [Google Scholar] [CrossRef]
  17. Saletti, R.; Muccilli, V.; Cunsolo, V.; Fontanini, D.; Capocchi, A.; Foti, S. MS-based characterization of αs2-casein isoforms in donkey’s milk. J. Mass Spectrom. 2012, 47, 1150–1159. [Google Scholar] [CrossRef]
  18. Malacarne, M.; Criscione, A.; Franceschi, P.; Bordonaro, S.; Formaggioni, P.; Marletta, D.; Summer, A. New insights into chemical and mineral composition of donkey milk throughout nine months of lactation. Animals 2019, 9, 1161. [Google Scholar] [CrossRef]
  19. Sargentini, C.; Tocci, R.; Martini, A.; Bozzi, R. Morphological characterization of Amiata donkey through Multivariate analyses. Rev. Bras. Zootec. 2018, 47, e20170310. [Google Scholar] [CrossRef]
  20. Rijnkels, M. Multispecies comparison of the casein gene loci and evolution of casein gene family. J. Mammary Gland. Biol. Neoplasia 2002, 7, 327–345. [Google Scholar] [CrossRef]
  21. Pauciullo, A.; Versace, C.; Gaspa, G.; Letaief, N.; Bedhiaf-Romdhani, S.; Fulgione, A.; Cosenza, G. Sequencing and Characterization of αs2-Casein Gene (CSN1S2) in the Old-World Camels Have Proven Genetic Variations Useful for the Understanding of Species Diversification. Animals 2023, 13, 2805. [Google Scholar] [CrossRef] [PubMed]
  22. Groenen, M.; Dijkhof, R.; Verstege, A.; Van der Poel, J. The complete sequence of the gene encoding bovine α2-casein. Gene 1993, 123, 187–193. [Google Scholar] [CrossRef] [PubMed]
  23. Ryskaliyeva, A.; Henry, C.; Miranda, G.; Faye, B.; Konuspayeva, G.; Martin, P. Alternative splicing events expand molecular diversity of camel CSN1S2 increasing its ability to generate potentially bioactive peptides. Sci. Rep. 2019, 9, 5243. [Google Scholar] [CrossRef] [PubMed]
  24. Cosenza, G.; Iannaccone, M.; Pico, B.A.; Ramunno, L.; Capparelli, R. The SNP g. 1311T> C associated with the absence of β-casein in goat milk influences CSN2 promoter activity. Anim. Genet. 2016, 47, 615–617. [Google Scholar] [CrossRef]
  25. Ramunno, L.; Cosenza, G.; Rando, A.; Pauciullo, A.; Illario, R.; Gallo, D.; Di Berardino, D.; Masina, P. Comparative analysis of gene sequence of goat CSN1S1 F and N alleles and characterization of CSN1S1 transcript variants in mammary gland. Gene 2005, 345, 289–299. [Google Scholar] [CrossRef]
  26. Ramunno, L.; Longobardi, E.; Pappalardo, M.; Rando, A.; Di Gregorio, P.; Cosenza, G.; Mariani, P.; Pastore, N.; Masina, P. An allele associated with a non-detectable amount of αs2 casein in goat milk. Anim. Genet. 2001, 32, 19–26. [Google Scholar] [CrossRef]
  27. Hong, D.; Jeong, S. 3’UTR diversity: Expanding repertoire of RNA alterations in human mRNAs. Mol. Cells 2023, 46, 48–56. [Google Scholar] [CrossRef]
  28. Navarro, E.; Mallén, A.; Hueso, M. Dynamic variations of 3′UTR length reprogram the mRNA regulatory landscape. Biomedicines 2021, 9, 1560. [Google Scholar] [CrossRef]
  29. Ferranti, P.; Chianese, L.; Malorni, A.; Migliaccio, F.; Stingo, V.; Addeo, F. Copresence of deleted protein species generates structural heterogeneity of ovine αs1-casein. J. Agric. Food Chem. 1998, 46, 411–416. [Google Scholar] [CrossRef]
  30. Ferranti, P.; Lilla, S.; Chianese, L.; Addeo, F. Alternative nonallelic deletion is constitutive of ruminant α s1-casein. J. Protein Chem. 1999, 18, 595–602. [Google Scholar] [CrossRef]
  31. Milenkovic, D.; Martin, P.; Guérin, G.; Leroux, C. A specific pattern of splicing for the horse α S1-Casein mRNA and partial genomic characterization of the relevant locus. Genet. Sel. Evol. 2002, 34, 509. [Google Scholar] [CrossRef]
  32. Martin, P.; Brignon, G.; Furet, J.; Leroux, C. The gene encoding αs1-casein is expressed in human mammary epithelial cells during lactation. Le Lait 1996, 76, 523–535. [Google Scholar] [CrossRef]
  33. Boisnard, M.; Hue, D.; Bouniol, C.; Mercier, J.C.; Gaye, P. Multiple mRNA species code for two non-allelic forms of ovine αs2-casein. Eur. J. Biochem. 1991, 201, 633–641. [Google Scholar] [CrossRef]
  34. Martin, P.; Szymanowska, M.; Zwierzchowski, L.; Leroux, C. The impact of genetic polymorphisms on the protein composition of ruminant milks. Reprod. Nutr. Dev. 2002, 42, 433–459. [Google Scholar] [CrossRef]
  35. Ramunno, L.; Cosenza, G.; Pappalardo, M.; Longobardi, E.; Gallo, D.; Pastore, N.; Di Gregorio, P.; Rando, A. Characterization of two new alleles at the goat CSN1S2 locus. Anim. Genet. 2001, 32, 264–268. [Google Scholar] [CrossRef]
  36. Cosenza, G.; Gallo, D.; Auzino, B.; Gaspa, G.; Pauciullo, A. Complete CSN1S2 Characterization, Novel Allele Identification and Association With Milk Fatty Acid Composition in River Buffalo. Front. Genet. 2021, 11, 622494. [Google Scholar] [CrossRef]
  37. Cosenza, G.; Pauciullo, A.; Feligini, M.; Coletta, A.; Colimoro, L.; Di Berardino, D.; Ramunno, L. A point mutation in the splice donor site of intron 7 in the αs2-casein encoding gene of the Mediterranean River buffalo results in an allele-specific exon skipping. Anim. Genet. 2009, 40, 791. [Google Scholar] [CrossRef]
  38. Bouniol, C.; Printz, C.; Mercier, J.-C. Bovine αs2-casein D is generated by exon VIII skipping. Gene 1993, 128, 289–293. [Google Scholar] [CrossRef]
  39. Brinkmann, J.; Koudelka, T.; Keppler, J.K.; Tholey, A.; Schwarz, K.; Thaller, G.; Tetens, J. Characterization of an equine α-S2-casein variant due to a 1.3 kb deletion spanning two coding exons. PLoS ONE 2015, 10, e0139700. [Google Scholar] [CrossRef]
  40. Cieslak, J.; Pawlak, P.; Wodas, L.; Borowska, A.; Stachowiak, A.; Puppel, K.; Kuczynska, B.; Luczak, M.; Marczak, L.; Mackowski, M. Characterization of equine CSN1S2 variants considering genetics, transcriptomics, and proteomics. J. Dairy Sci. 2016, 99, 1277–1285. [Google Scholar] [CrossRef]
  41. Balteanu, V.A.; Carsai, T.C.; Vlaic, A. Identification of an intronic regulatory mutation at the buffalo α S1-casein gene that triggers the skipping of exon 6. Mol. Biol. Rep. 2013, 40, 4311–4316. [Google Scholar] [CrossRef]
  42. De Pascale, S.; Caira, S.; Garro, G.; Mauriello, R.; Scaloni, A.; Cosenza, G.; Chianese, L. Proteomic characterisation and phylogenetic derivation of ovine αS1-CN B and αS1-CN G genetic variants. Int. Dairy J. 2022, 131, 105387. [Google Scholar] [CrossRef]
  43. Giambra, I.J.; Chianese, L.; Ferranti, P.; Erhardt, G. Short communication: Molecular genetic characterization of ovine alpha(S1)-casein allele H caused by alternative splicing. J. Dairy Sci. 2010, 93, 792–795. [Google Scholar] [CrossRef]
  44. Lenasi, T.; Rogelj, I.; Dovc, P. Characterization of equine cDNA sequences for αS1-, β-and κ-casein. J. Dairy Res. 2003, 70, 29–36. [Google Scholar] [CrossRef]
  45. Pauciullo, A.; Gauly, M.; Cosenza, G.; Wagner, H.; Erhardt, G. Lama glama αS1-casein: Identification of new polymorphisms in the CSN1S1 gene. J. Dairy Sci. 2017, 100, 1282–1289. [Google Scholar] [CrossRef]
  46. Alexander, L.; Beattie, C. The sequence of porcine αs1-casein cDNA: Evidence for protein variants generated by altered RNA splicing. Anim. Genet. 1992, 23, 283–288. [Google Scholar] [CrossRef]
  47. Gu, M.; Cosenza, G.; Nicolae, I.; Bota, A.; Guo, Y.; Di Stasio, L.; Pauciullo, A. Transcript analysis at DGAT1 reveals different mRNA profiles in river buffaloes with extreme phenotypes for milk fat. J. Dairy Sci. 2017, 100, 8265–8276. [Google Scholar] [CrossRef]
  48. Brinkmann, J.; Jagannathan, V.; Drögemüller, C.; Rieder, S.; Leeb, T.; Thaller, G.; Tetens, J. Genetic variability of the equine casein genes. J. Dairy Sci. 2016, 99, 5486–5497. [Google Scholar] [CrossRef]
  49. Giambra, I.; Erhardt, G. Molecular genetic characterization of ovine CSN1S2 variants C and D reveal further important variability within CSN1S2. Anim. Genet. 2012, 43, 642–645. [Google Scholar] [CrossRef]
  50. Farrell Jr, H.; Jimenez-Flores, R.; Bleck, G.; Brown, E.; Butler, J.; Creamer, L.; Hicks, C.; Hollar, C.; Ng-Kwai-Hang, K.; Swaisgood, H. Nomenclature of the proteins of cows’ milk—Sixth revision. J. Dairy Sci. 2004, 87, 1641–1674. [Google Scholar] [CrossRef]
  51. Cosenza, G.; Albarella, S.; D’Anza, E.; Iannuzzi, A.; Selvaggi, M.; Pugliano, M.; Galli, T.; Saralli, G.; Ciotola, F.; Peretti, V. A New AS-PCR Method to Detect CSN2 01 Allele, Genotyping at Ca-Sensitive Caseins Loci and Milk Traits Association Studies in Autochthonous Lazio Goats. Animals 2023, 13, 239. [Google Scholar] [CrossRef] [PubMed]
  52. Di Gerlando, R.; Tortorici, L.; Sardina, M.T.; Monteleone, G.; Mastrangelo, S.; Portolano, B. Molecular Characterisation of κ–Casein Gene in Girgentana Dairy Goat Breed and Identification of Two New Alleles. Ital. J. Anim. Sci. 2015, 14, 3464. [Google Scholar] [CrossRef]
  53. Pazzola, M.; Vacca, G.M.; Noce, A.; Porcedda, M.; Onnis, M.; Manca, N.; Dettori, M.L. Exploring the genotype at CSN3 gene, milk composition, coagulation and cheese-yield traits of the sardo-modicana, an autochthonous cattle breed from the Sardinia Region, Italy. Animals 2020, 10, 1995. [Google Scholar] [CrossRef] [PubMed]
  54. Anagnostou, M.; Chung, C.; McGann, E.; Verheijen, B.; Kou, Y.; Chen, L.; Vermulst, M. Transcription errors in aging and disease. Transl. Med. Aging 2021, 5, 31–38. [Google Scholar] [CrossRef]
  55. Fritsch, C.; Gout, J.-F.P.; Vermulst, M. Genome-wide surveillance of transcription errors in eukaryotic organisms. JoVE (J. Vis. Exp.) 2018, 139, e57731. [Google Scholar]
  56. Mohr, U.; Koczan, D.; Linder, D.; Hobom, G.; Erhardt, G. A single point mutation results in A allele-specific exon skipping in the bovine αs1-casein mRNA. Gene 1994, 143, 187–192. [Google Scholar] [CrossRef]
  57. Cosenza, G.; Iannaccone, M.; Auzino, B.; Macciotta, N.; Kovitvadhi, A.; Nicolae, I.; Pauciullo, A. Remarkable genetic diversity detected at river buffalo prolactin receptor (PRLR) gene and association studies with milk fatty acid composition. Anim. Genet. 2018, 49, 159–168. [Google Scholar] [CrossRef] [PubMed]
  58. Cosenza, G.; Iannaccone, M.; Pico, A.B.; Gallo, D.; Capparelli, R.; Pauciullo, A. Molecular characterisation, genetic variability and detection of a functional polymorphism influencing the promoter activity of OXT gene in goat and sheep. J. Dairy Res. 2017, 84, 165–169. [Google Scholar] [CrossRef]
  59. Pauciullo, A.; Versace, C.; Miretti, S.; Giambra, I.; Gaspa, G.; Letaief, N.; Cosenza, G. Genetic variability among and within domestic Old and New World camels at the α-lactalbumin gene (LALBA) reveals new alleles and polymorphisms responsible for differential expression. J. Dairy Sci. 2024, 107, 1068–1084. [Google Scholar] [CrossRef]
  60. Klein, J. Origin of major histocompatibility complex polymorphism: The trans-species hypothesis. Hum. Immunol. 1987, 19, 155–162. [Google Scholar] [CrossRef]
  61. Zachos, F.E. Mammalian phylogenetics: A short overview of recent advances. In Mammals of Europe-Past, Present, and Future; Springer: Cham, Switzerland, 2020; pp. 31–48. [Google Scholar]
Animals 14 02918 g001
Figure 1. Nucleotide sequences of cDNA clones coding for αs2-CN-I. Dashes represent identical nucleotides to those in the upper lines. The deduced protein sequence is shown above each corresponding nucleotide sequence. The large arrows indicate exons of the mRNA as deduced from known splice junctions of the donkey CSN1S2 I gene [12]. Exon numbering (above the blocks) follows the method of Cosenza et al. [12]. Exon 12′ is an additional exon compared to the donkey CSN1S2 I cDNA sequence (FM946022.1); therefore, it is numbered with a prime (′). Gray boxes depict skipped exons or sequences absent from the sequenced cDNA clones. The stop codon is indicated by an asterisk (*). The exon 17 gt cryptic splice site is in bold. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).
Figure 1. Nucleotide sequences of cDNA clones coding for αs2-CN-I. Dashes represent identical nucleotides to those in the upper lines. The deduced protein sequence is shown above each corresponding nucleotide sequence. The large arrows indicate exons of the mRNA as deduced from known splice junctions of the donkey CSN1S2 I gene [12]. Exon numbering (above the blocks) follows the method of Cosenza et al. [12]. Exon 12′ is an additional exon compared to the donkey CSN1S2 I cDNA sequence (FM946022.1); therefore, it is numbered with a prime (′). Gray boxes depict skipped exons or sequences absent from the sequenced cDNA clones. The stop codon is indicated by an asterisk (*). The exon 17 gt cryptic splice site is in bold. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).
Animals 14 02918 g001
Animals 14 02918 g002
Figure 2. Nucleotide sequences of cDNA clones coding for αs2-CN-II. Dashes represent identical nucleotides to those in the upper lines. The deduced protein sequence is shown above each corresponding nucleotide sequence. The large arrows indicate exons of the mRNA as deduced from known splice junctions of the donkey CSN1S2 II gene [12]. Exon numbering (above the blocks) follows the method of Cosenza et al. [12]. Ex 7′ is an additional exon compared to the donkey CSN1S2 II cDNA sequence (FN298386.2); therefore, it is numbered with a prime (′). Gray boxes depict skipped exons or sequences absent from the sequenced cDNA clones. The stop codon is indicated by an asterisk (*). The exon 13 gt cryptic splice site is in bold. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).
Figure 2. Nucleotide sequences of cDNA clones coding for αs2-CN-II. Dashes represent identical nucleotides to those in the upper lines. The deduced protein sequence is shown above each corresponding nucleotide sequence. The large arrows indicate exons of the mRNA as deduced from known splice junctions of the donkey CSN1S2 II gene [12]. Exon numbering (above the blocks) follows the method of Cosenza et al. [12]. Ex 7′ is an additional exon compared to the donkey CSN1S2 II cDNA sequence (FN298386.2); therefore, it is numbered with a prime (′). Gray boxes depict skipped exons or sequences absent from the sequenced cDNA clones. The stop codon is indicated by an asterisk (*). The exon 13 gt cryptic splice site is in bold. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).
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Animals 14 02918 g003
Figure 3. Comparison of deduced Equus asinus (present work) and Bos taurus (GenBank: AAI14774.1) amino acid sequences of mature αs2-casein. Major bovine IgE-binding regions (corresponding amino acid sequences: 83–100 and 165–188) are in bold. Donkey sequences 92NKINQ96 and 176NKINQ180 are shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).
Figure 3. Comparison of deduced Equus asinus (present work) and Bos taurus (GenBank: AAI14774.1) amino acid sequences of mature αs2-casein. Major bovine IgE-binding regions (corresponding amino acid sequences: 83–100 and 165–188) are in bold. Donkey sequences 92NKINQ96 and 176NKINQ180 are shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).
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Figure 4. Observed genotypes after XbaI (T/CTAGA) digestion of PCR-amplified fragments spanning exon 17 and its flanking regions in donkeys carrying the FM946022.1: c.375-1G>A mutation in the splice acceptor site of exon 17 in the CSN1S2 I gene. Lane 1, AA homozygous sample; lane 2, heterozygous sample; lane 3, GG homozygous sample. The marker (M) used is the 1kb Opti-DNA Ladder (0.1–10 kb) (Applied Biological Materials, ABM, Vancouver, BC, Canada).
Figure 4. Observed genotypes after XbaI (T/CTAGA) digestion of PCR-amplified fragments spanning exon 17 and its flanking regions in donkeys carrying the FM946022.1: c.375-1G>A mutation in the splice acceptor site of exon 17 in the CSN1S2 I gene. Lane 1, AA homozygous sample; lane 2, heterozygous sample; lane 3, GG homozygous sample. The marker (M) used is the 1kb Opti-DNA Ladder (0.1–10 kb) (Applied Biological Materials, ABM, Vancouver, BC, Canada).
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Table 1. Ragusana donkey CSN1S2 I mRNAs identified through clone screening and comparison with donkey CSN1S2 I transcripts characterized in previous studies.
Table 1. Ragusana donkey CSN1S2 I mRNAs identified through clone screening and comparison with donkey CSN1S2 I transcripts characterized in previous studies.
Present WorkAuzino et al. [7]Saletti et al. [17]
Cunsolo et al. [16]		Deduced Mature Protein Size (aa)Theoretical Mw
Correctly assembled-Correctly assembled22126,030.19
Alternative skippingLacking exon 11--20624,116.04
Insertion exon 12′--14316,617.68
-Lacking exon 3 and 3′ end of exon 17-20524,145.24
Lacking exons 4, 5, 6, and 3′ end of exon 17Lacking exons 4, 5, 6, and 3′ end of exon 17Lacking exons 4, 5, 6, and 3′ end of exon 1718321,713.42
Lacking 3′ end of exon 17Lacking 3′ end of exon 17Lacking 3′ end of exon 1721425,203.33
Lacking exons 4, 5, and 6Lacking exons 4, 5, and 6-19022,540.28
-Lacking exons 4, 5, 6, and 13-18121,490.19
-Lacking exon 6 and 3′ end of exon 17-20524,263.32
Lacking exons 4, 5, 6, and 5′ of exon 17-Lacking exons 4, 5, 6, and 5′ of exon 1718521,942.60
Lacking 5′ of exon 17-Lacking 5′ of exon 1721625,432.52
Table 2. Ragusana donkey CSN1S2 II mRNAs identified through clone screening and comparison with Amiatina donkey CSN1S2 II transcripts characterized by Auzino et al. [7].
Table 2. Ragusana donkey CSN1S2 II mRNAs identified through clone screening and comparison with Amiatina donkey CSN1S2 II transcripts characterized by Auzino et al. [7].
Present WorkAuzino et al. [7]Deduced Mature Protein Size (aa)Theoretical Mw
Correctly assembled with or without exon 15 14216,377.88
Alternative skippingInsertion exon 7′ 15718,236.13
Lacking exon 9 and
insertion exon 7′		 14917,314.17
Lacking exon 3 and
insertion exon 7′		14817,239.06
Lacking exons 3, 9, and
insertion exon 7′		14016,317.10
Lacking exons 3, 11, 12, first 33nt exon 13, and insertion exon 7′11413,308.63
Lacking exon 9 13415,455.92
Lacking exon 10 13315,358.65
Lacking exons 11, 12, and first 33nt exon 13
with or without exon 15		 10812,447.45
Lacking exons 9, 10, and 15 12514,436.69
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Cosenza, G.; Pauciullo, A. A Comprehensive Analysis of CSN1S2 I and II Transcripts Reveals Significant Genetic Diversity and Allele-Specific Exon Skipping in Ragusana and Amiatina Donkeys. Animals 2024, 14, 2918. https://doi.org/10.3390/ani14202918

AMA Style

Cosenza G, Pauciullo A. A Comprehensive Analysis of CSN1S2 I and II Transcripts Reveals Significant Genetic Diversity and Allele-Specific Exon Skipping in Ragusana and Amiatina Donkeys. Animals. 2024; 14(20):2918. https://doi.org/10.3390/ani14202918

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Cosenza, Gianfranco, and Alfredo Pauciullo. 2024. "A Comprehensive Analysis of CSN1S2 I and II Transcripts Reveals Significant Genetic Diversity and Allele-Specific Exon Skipping in Ragusana and Amiatina Donkeys" Animals 14, no. 20: 2918. https://doi.org/10.3390/ani14202918

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