Next Article in Journal
Genetic Demography of the Blue and Red Shrimp, Aristeus antennatus: A Female-Based Case Study Integrating Multilocus Genotyping and Morphometric Data
Next Article in Special Issue
FISH Mapping of Telomeric and Non-Telomeric (AG3T3)3 Reveal the Chromosome Numbers and Chromosome Rearrangements of 41 Woody Plants
Previous Article in Journal
Complete Chloroplast Genome of an Endangered Species Quercus litseoides, and Its Comparative, Evolutionary, and Phylogenetic Study with Other Quercus Section Cyclobalanopsis Species
Previous Article in Special Issue
Near-Hexaploid and Near-Tetraploid Aneuploid Progenies Derived from Backcrossing Tetraploid Parents Hibiscus syriacus × (H. syriacus × H. paramutabilis)
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Cytogenetic Analysis of the Members of the Snake Genera Cylindrophis, Eryx, Python, and Tropidophis

by
Tomáš Charvát
1,
Barbora Augstenová
1,
Daniel Frynta
2,
Lukáš Kratochvíl
1 and
Michail Rovatsos
1,*
1
Department of Ecology, Faculty of Science, Charles University, Viničná 7, 12844 Prague, Czech Republic
2
Department of Zoology, Faculty of Science, Charles University, Viničná 7, 12844 Prague, Czech Republic
*
Author to whom correspondence should be addressed.
Genes 2022, 13(7), 1185; https://doi.org/10.3390/genes13071185
Submission received: 15 May 2022 / Revised: 25 June 2022 / Accepted: 28 June 2022 / Published: 1 July 2022
(This article belongs to the Special Issue Chromosome Evolution and Karyotype Analysis)

Abstract

:
The recent discovery of two independently evolved XX/XY sex determination systems in the snake genera Python and Boa sparked a new drive to study the evolution of sex chromosomes in poorly studied lineages of snakes, where female heterogamety was previously assumed. Therefore, we examined seven species from the genera Eryx, Cylindrophis, Python, and Tropidophis by conventional and molecular cytogenetic methods. Despite the fact that these species have similar karyotypes in terms of chromosome number and morphology, we detected variability in the distribution of heterochromatin, telomeric repeats, and rDNA loci. Heterochromatic blocks were mainly detected in the centromeric regions in all species, although accumulations were detected in pericentromeric and telomeric regions in a few macrochromosomes in several of the studied species. All species show the expected topology of telomeric repeats at the edge of all chromosomes, with the exception of Eryx muelleri, where additional accumulations were detected in the centromeres of three pairs of macrochromosomes. The rDNA loci accumulate in one pair of microchromosomes in all Eryx species and in Cylindrophis ruffus, in one macrochromosome pair in Tropidophis melanurus and in two pairs of microchromosomes in Python regius. Sex-specific differences were not detected, suggesting that these species likely have homomorphic, poorly differentiated sex chromosomes.

1. Introduction

Snakes (Serpentes) are a diverse group of squamate reptiles, with approximately 3970 species, representing roughly one-third of the total reptile species diversity [1]. The majority of extant species of snake belong to the group Caenophidia (3283 species), while the rest are divided into two major groups: Henophidia (228 species, mainly boas and pythons) and Scolecophidia (466 species, commonly known as blind snakes or thread snakes) [1]. These two groups are, however, mostly recognized due to historical reasons, as they are paraphyletic according to recent phylogenetic reconstructions [2,3,4,5]. Despite their striking diversity, snakes have quite conserved karyotypes. Although their diploid chromosome number varies between 2n = 24 and 2n = 56 [6,7,8], the most common chromosome number found in the majority of snake lineages is 2n = 36, with 16 macrochromosomes and 20 microchromosomes [7,8].
So far, only genotypic sex determination has been documented in snakes [9]. While homologous, highly differentiated and often heteromorphic ZZ/ZW sex chromosomes or derived systems of multiple sex chromosomes were reported in all examined caenophidian species [10,11,12,13,14,15], we still have limited knowledge on the sex chromosome evolution in henophidian and scolecophidian snakes. Heteromorphic ZZ/ZW sex chromosomes were detected in the henophidian Madagascar boa Acrantophis sp. cf. dumerili (Sanziniidae) [13,16] and, very recently, in the scolecophidian Myriopholis macrorhyncha [17]. Nevertheless, cytogenetic analyses did not reveal sex chromosomes in other henophidian or scolecophidian species, and in many older studies, only one sex was examined [8,13,18,19,20,21,22,23]. Furthermore, sex chromosomes were not detected in Boa constrictor, neither by comparative read depth (genome coverage) analysis nor by Illumina reads between sexes [24]. For decades, it was speculated that all snakes might have homologous ZZ/ZW sex chromosomes, which are heteromorphic and highly differentiated in caenophidian snakes but homomorphic and poorly differentiated in henophidian and scolecophidian snakes [20,21,24,25,26]. However, this view was proved incorrect when two non-homologous XX/XY systems were detected in a python (Python bivittatus; Pythonidae) and two species of boa (Boa constrictor, B. imperator; Boidae) by single-nucleotide polymorphism (SNP) analysis of RAD-seq genomic data [27]. Notably, the sex chromosomes of P. bivittatus are partially homologous to ZZ/ZW sex chromosomes of caenophidian snakes, while the sex chromosomes in the two boas are homologous to an autosome of caenophidian snakes. These recent cytogenetic and genomic findings have revived the interest of the scientific community to further explore the evolution of sex chromosomes in snakes.
In the present study, we cytogenetically examined seven henophidian species: the sand boas Eryx colubrinus, E. conicus, E. miliaris, and E. muelleri (Erycidae); the ball python Python regius (Pythonidae); the red-tailed pipe snake Cylindrophis ruffus (Cylindrophiidae); and the Cuban wood snake Tropidophis melanurus (Tropidophiidae). Our aim was to expand our knowledge on the karyotypic traits of these species, with emphasis on exploring the presence of sex chromosomes. The selected species have a potentially phylogenetically informative position for the reconstruction of sex chromosome evolution in snakes. T. melanurus is a member of the lineage Amerophidia and sister to all other henophidian and caenophidian snakes [2,5]. The ball python P. regius is closely related to P. bivittatus, a species with an XX/XY sex determination system [27], and C. ruffus is a member of the lineage relatively closely related to pythons [2,5]. The sand boas of the genus Eryx are phylogenetically nested between lineages of boas with documented ZZ/ZW (A. sp. cf. dumerili) and XX/XY (B. constrictor, B. imperator) sex chromosomes. We applied conventional (karyotype reconstruction and C-banding) and molecular (in situ hybridization with probes for telomeric repeats and rDNA loci and comparative genome hybridization) cytogenetic methods. The presence of telomeric repeats in the interstitial parts of chromosomes might help uncover cryptic chromosomal rearrangements and further expand the knowledge of karyotype evolution [28]. Furthermore, heterochromatin, rDNA loci, and telomeric repeats tend to accumulate on reptile sex chromosomes [15,29,30,31,32,33], and may be suitable markers for identifying homomorphic sex chromosomes.

2. Materials and Methods

2.1. Samples and Species Verification

Seven non-caenophidian snake species were used for this study. We examined specimens of both sexes of Eryx colubrinus, E. conicus, E. miliaris, E. muelleri (Erycidae), and Python regius (Pythonidae), but only female specimens of Cylindrophis ruffus (Cylindrophiidae) and Tropidophis melanurus (Tropidophiidae) (Table 1). All animals were obtained from the pet trade and were either captive-bred or legally imported from the wild. Blood samples were collected from each individual, and were used for extraction of DNA and leukocyte cultivation for preparation of chromosome suspensions.
Because taxon identification based on external morphology can often be unreliable, and taxonomic nomenclature is occasionally revised in snakes, we chose to provide the sequences of the mitochondrial loci cytochrome b (cytb) and cytochrome c oxidase subunit I (coi) as a genetic identity of the individuals that we cytogenetically examined (see Rovatsos et al. [34]). For this task, DNA was isolated from fresh blood samples using a DNeasy Blood and Tissue Kit (Qiagen, Hilden, Germany). To amplify the desirable mitochondrial regions, we used primers RepCOI-F/RepCOI-R [35] and L14919/H16064 [36,37] for coi and cytb, respectively. The parameters of the PCR and amplification conditions were previously reported in Koubová et al. [38] and Mazzoleni et al. [39]. The PCR products were sent for bi-directional Sanger sequencing to Macrogen (Korea). The sequences were trimmed and aligned in Geneious Prime v.2022.1.1 (https://www.geneious.com, accessed on 6 May 2022) and compared with other available sequences in the GenBank database using BLAST [40].

2.2. Chromosome Preparation and Staining

Chromosome suspensions were obtained via leukocyte cultivation from fresh whole-blood samples as in Mazzoleni et al. [39]. Slides with chromosome spreads were stained by Giemsa for evaluation of the quality of the chromosome suspension and for karyogram reconstruction. Karyograms were reconstructed using the Ikaros karyotyping system (MetaSystems, Altlussheim, Germany).
The topology of constitutive heterochromatin was visualized using the standard C-banding protocol [41] but Fluoroshield with DAPI (Vector Laboratories, Burlingame, CA, USA), instead of Giemsa, was used to stain the chromosomal material. The studied species differed in the minimal BaOH2 treatment time needed to sufficiently visualize the heterochromatic blocks: 5 min for Eryx colubrinus and Cylindrophis ruffus, 8 min for Python regius, 10 min for E. miliaris, 15 min for E. conicus, and 18 min for E. muelleri and Tropidophis melanurus.

2.3. Fluorescence In Situ Hybridization (FISH) with Probes for Repetitive Elements

FISH with a telomeric probe was performed to visualize the distribution of telomeric-like sequences and, moreover, to uncover putative interstitial telomeric repeats. The probe with the (TTAGGG)n motif was prepared by PCR without a template, according to our published protocol (Rovatsos et al. [34], based on Ijdo et al. [42]). Plasmid (pDmr.a 51#1) with an 11.5 kb insert encoding the 18S and 28S ribosomal units of Drosophila melanogaster [43] was used for rDNA probe preparation. It was cut to 200–300 bp long fragments and labeled with dUTP-biotin by nick translation (Abbott Molecular, Des Plaines, IL, USA). Probes were precipitated using salmon sperm, sodium acetate (3M), and 96% ice-cold ethanol, and resuspended in hybridization buffer (50% formamide in 2 × SSC). The treatment of the chromosome suspensions and the probe, the hybridization conditions, the post-hybridization washes, and the signal amplification were performed following the protocols from Rovatsos et al. [28] and Mazzoleni et al. [39].

2.4. Comparative Genome Hybridization (CGH)

DNA samples from males were labeled with dUTP-biotin (Roche, Basel, Switzerland), while DNA samples from females were labeled with dUTP-digoxigenin (Roche, Basel, Switzerland) using nick translation (Abbott Laboratories, Lake Bluff, IL, USA), according to the manufacturer’s protocol. Labeled DNA samples from a male and a female specimen of the same species were mixed in equal concentration, purified by ethanol precipitation, and resuspended in hybridization buffer (50% formamide in 2 × SSC). The treatment of chromosome suspensions and probes, the hybridization conditions, the post-hybridization washes and the signal detection were performed following the protocol from Rovatsos et al. [44].

2.5. Microscopy Analysis

Giemsa-stained metaphases were captured on a Zeiss Axio Imager Z2 microscope equipped with an automatic Metafer-MSearch scanning platform and a CoolCube 1 b/w digital camera (MetaSystems, Altlussheim, Germany). Metaphases stained with C-banding and in situ hybridization techniques were captured with a Provis AX70 fluorescence microscope equipped with a DP30BW digital camera (Olympus, Tokyo, Japan). All images were acquired in black and white, and later processed using DP Manager imaging software (Olympus, Tokyo, Japan).

3. Results

3.1. Karyotype Reconstruction

All four tested species of sand boas have karyotypes with 2n = 34 chromosomes. Eryx conicus, E. muelleri, and E. miliaris have karyotypes with 16 macrochromosomes and 18 microchromosomes and share similar chromosome morphology. Pairs 1, 3, and 4 are metacentric, while pair 2 is submetacentric, and the remaining macrochromosomes are acrocentric. The morphology of the microchromosomes was not distinguishable (Figure 1c–h). E. colubrinus has 20 macrochromosomes and 14 microchromosomes. Chromosome pairs 9 and 10, which are microchromosomes in other sand boas, are much larger in this species. Chromosome pair 9 is submetacentric, while pair 10 is acrocentric (Figure 1a,b).
Tropidophis melanurus also has a diploid chromosome number of 2n = 34, with 22 macrochromosomes and 12 microchromosomes. Pairs 1–4 are submetacentric, and the remaining macrochromosome pairs are acrocentric (Figure 1l).
The karyotypes of Cylindrophis ruffus and Python regius have 2n = 36 chromosomes, with 16 macrochromosomes and 20 microchromosomes. Pairs 1, 3, and 4 are metacentric, pair 2 is submetacentric, while pairs 5–8 are acrocentric (Figure 1i–k).
Heteromorphic sex chromosomes were not detected in any of the tested snake species.

3.2. C-Banding

In Python regius, constitutive heterochromatin is located in the centromeric region of all chromosomes and in the pericentromeric region of chromosome pairs 1 and 6 (Figure 2i,j). In addition to centromeric heterochromatin, all sand boas and Cylindrophis ruffus have heterochromatic blocks in the terminal region of the q-arm of the second largest chromosome pair (Figure 2a–h,k). A similar signal in the first largest chromosome pair is present in Tropidophis melanurus (Figure 2l). Furthermore, Tropidophis melanurus has an extensive accumulation of heterochromatin at the centromere and at the interstitial position of the sixth macrochromosome pair (Figure 2l).
We detected intraspecific heterochromatin heteromorphism in both males and females of two sand boa species. A large heterochromatin block was found in the pericentric region of one chromosome from the fourth largest pair in a male and a female of Eryx miliaris (Figure 2e,f), which is missing in the other four conspecific individuals in both sexes. On the other hand, all four studied individuals of E. colubrinus display heterochromatin heteromorphism in the telomeric region of the q-arm on one chromosome from the seventh pair. This species has heterochromatin blocks in the pericentromeric region on the q-arms of chromosome pairs 4, 5, 6 and 8. Chromosome pairs 9 and 10 are highly heterochromatic (Figure 2a,b).
Sex-specific differences in the heterochromatin distribution were not detected in any of the examined species.

3.3. Fluorescence In Situ Hybridization

The signal from FISH with the telomeric probe was detected in the expected terminal regions of all chromosomes in all tested species (Figure 3). In addition, Eryx muelleri has interstitial telomeric repeats (ITRs) in the centromeric region of the first three largest chromosome pairs (Figure 3g,h).
The rDNA loci are located on one macrochromosome pair in Tropidophis melanurus; one microchromosome pair in Eryx colubrinus, E. conicus, E. miliaris, E. muelleri, and Cylindrophis ruffus; and on two microchromosome pairs in Python regius (Figure 4). Sex-specific differences were not detected in the topology of rDNA loci or telomeric repeats in any of the studied species.

3.4. Comparative Genome Hybridization

CGH experiments were performed for all tested species from the genus Eryx and for the species Python regius, where DNA and chromosome suspensions were available from both sexes. However, sex-specific differences were not detected in these species (Figure 5).

4. Discussion

To the best of our knowledge, the karyotypes of five out of seven included snake species were presented here for the first time, specifically for Eryx colubrinus, E. miliaris, E. muelleri, Python regius, and Tropidophis melanurus.
In accordance with previous studies [11,45,46], we conclude that all species of sand boas so far examined share a diploid chromosome number of 2n = 34, which is possibly an apomorphy of Erycidae, as species from closely related groups have mostly 2n = 36 chromosomes [7,13,23,47,48]. However, while all other sand boas have 16 macrochromosomes and 18 microchromosomes and share chromosome morphology, E. colubrinus has 20 macrochromosomes and 14 microchromosomes. It is likely that two pairs of former microchromosomes increased in size in this species, as the morphology of other chromosomes is otherwise shared with the rest of the sand boas. Both of these pairs also contain large heterochromatic blocks, which likely play a role in the aforementioned size difference, either by amplification of repetitive elements or translocation from another chromosome and further heterochromatinization.
Polymorphism in the distribution of heterochromatin was found in all tested individuals of E. colubrinus and in two out of six studied individuals of E. miliaris. Heterochromatin heteromorphism was previously described in numerous species of vertebrates [49,50,51,52,53]. Notably, in several species of newt of the genus Triturus, all individuals are heterozygous in certain chromatin blocks, as homozygosity in them is lethal [54]. A similar case of heterochromatin heteromorphism was recently documented in Malagasy tomato frogs from the genus Dyscophus [55].
T. melanurus has a diploid chromosome number of 2n = 34 (22 macrochromosomes and 12 microchromosomes), which is surprising as the only other member of the family Tropidophiidae with the reported chromosome number has 2n = 26 [56] in [8]. Such variability in diploid chromosome numbers is rare in snakes, and it has been reported in a few lineages, such as the tree boas of the genus Corallus [22] and the Malagasy snakes of the subfamily Pseudoxyrhophiinae [57], so further examination of additional species from the family Tropidophiidae may help us to better understand the karyotype evolution in this group.
rDNA loci typically accumulate in a single pair of microchromosomes in henophidian snakes [22,58,59,60], except for Candoia paulsoni, which has an additional accumulation on a second pair of macrochromosomes [23]. All examined species of the genus Eryx as well as C. ruffus show clusters of rDNA loci on one pair of microchromosomes. However, we uncovered the presence of rDNA loci on two microchromosome pairs in Python regius, even though such a pattern has not been described in other pythons and despite their generally conserved karyotypes [17,23,58]. On the contrary, rDNA loci seem to accumulate on one pair of macrochromosomes in T. melanurus. Such cases of rDNA loci accumulation in macrochromosomes have been reported in a few species of caenophidian and scolecophidian snakes [17,58,61], which can be explained either by (i) chromosome fusion of the ancestral rDNA loci-carrying microchromosome with a macrochromosome, or (ii) translocation of rDNA loci to a macrochromosome.
We detected ITRs in the centromeric region of macrochromosome pairs 1–3 in E. muelleri but not in other sand boas. Considering that the chromosome morphology of this species is shared with other sand boas (except for E. colubrinus, as mentioned above), we suppose that ITRs in this species are likely an outcome of cryptic intrachromosomal rearrangements, such as inversions. Furthermore, the centromeric satellite content is very dynamic, and even closely related species might have a different composition of repeats [23,62,63,64]. FISH with telomeric probes did not detect ITRs in T. melanurus; however, the presence of the interstitial heterochromatin on the sixth chromosome pair might suggest a possible fusion point (e.g., tandem fusion), which might also explain the lower chromosome number (2n = 34) in this species compared with the typical snake karyotype (2n = 36). We conclude that the distribution of ITRs and rDNA loci, although generally stable on a larger scale, might be quite variable even among closely related snake species despite similarities in chromosome morphology [17,23,65]. Notably, the intense signal of telomeric repeats was detected in the majority of the microchromosomes in snakes of the genus Eryx (Figure 3). These microchromosomes are tiny and dot-like; therefore, we cannot safely conclude whether the intense signal derives from ITRs or the extended arrays of terminal telomeres. A similar pattern has been identified in other reptilian species, such as the dragonsnake Xenodermus javanicus [66], monitors, and helodermatids [28,63]. One potential explanation is that microchromosomes often have higher recombination rates than autosomes in vertebrates, including birds and snakes [67,68,69]. We speculate that the repair of the breaks occurring in DNA strands during recombination might lead to the incorporation of telomeric repeats, as telomerase, the enzyme that synthesizes telomeric sequences, is often involved in DNA repair [70]. The evolutionary or functional significance of a higher number of telomeric copies in microchromosomes is not fully understood and deserves further investigation in the future.
Although the methods used in this study had proved effective for uncovering sex chromosomes in some squamate lineages in the past, they did not reveal any sex-specific differences in the examined snake species. This is true even for Python regius, where X and Y sex chromosomes are expected due to the observed pattern of inheritance of a partially sex-linked phenotypic trait [71] and for which there are reports of facultative parthenogenesis, which leads to all-female offspring [72]. The Madagascar boa A. sp. cf. dumerili remains the only henophidian snake with detected heteromorphic sex chromosomes. This snake seems to have evolved heteromorphic sex chromosomes by an inversion, but its Z and W are probably poorly differentiated at the sequence level, as CGH did not reveal any female-specific pattern on its W chromosome [16]. Thus, we can conclude that all tested Eryx species and P. regius have poorly differentiated sex chromosomes similar to almost all of the other studied henophidian snakes. Male individuals of C. ruffus and T. melanurus should be examined in the future to investigate the possible presence of heteromorphic sex chromosomes. However, we cannot rule out that environmental sex determination might also be present in some henophidian snakes, although it has not yet been reported in any snake [9]. Poorly differentiated sex chromosomes are more prone to turnovers than highly differentiated sex chromosomes [73], which can—together with differences in lineage ages—explain the emerging pattern of the higher variability in sex chromosome systems in snakes from the scolecophidian and henophidian groups compared with the evolutionary stable ZZ/ZW sex chromosomes of caenophidian snakes [14,16,24,27]. Molecular methods such as RAD-seq or whole-genome coverage analyses have been successful in uncovering sex determination systems not only in snakes but also in other squamate lineages with poorly differentiated sex chromosomes [27,74,75,76], and might offer a way to resolve sex determination systems in scolecophidian and henophidian snakes in the future.

Author Contributions

Conceptualization, M.R.; investigation, T.C. and B.A.; resources, T.C., B.A., D.F., L.K. and M.R.; writing—original draft preparation, T.C., L.K. and M.R.; writing—review and editing, T.C., B.A., D.F., L.K. and M.R.; visualization, T.C.; funding acquisition, T.C., L.K. and M.R. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by the Czech Science Foundation (GAČR 20-27236J), Charles University Grant Agency (GAUK 358522) and the Charles University Research Centre program (204069).

Institutional Review Board Statement

Animal handling and collection of blood samples were performed by accredited researchers (LK: CZ02535, MR: CZ03540). The experimental procedures were approved by the Ethics Committee of the Faculty of Science, Charles University, and the Committee for Animal Welfare of the Ministry of Agriculture of the Czech Republic (permit No. MSMT-8604/2019-7).

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We would like to express our gratitude to Petr Ráb and members of his laboratory for their support and Jana Thomayerová for providing technical support.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Uetz, P.; Freed, P.; Aguilar, R.; Hošek, J. (Eds.) The Reptile Database. 2022. Available online: http://www.reptile-database.org (accessed on 11 April 2022).
  2. Pyron, R.A.; Burbrink, F.T.; Wiens, J.J. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes. BMC Evol. Biol. 2013, 13, 93. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Pyron, R.A.; Wallach, V. Systematics of the blindsnakes (Serpentes: Scolecophidia: Typhlopoidea) based on molecular and morphological evidence. Zootaxa 2014, 3829, 1–81. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Reynolds, R.G.; Niemiller, M.L.; Revell, L.J. Toward a Tree-of-Life for the boas and pythons: Multilocus species-level phylogeny with unprecedented taxon sampling. Mol. Phylogenet. Evol. 2014, 71, 201–213. [Google Scholar] [CrossRef] [PubMed]
  5. Zheng, Y.; Wiens, J.J. Combining phylogenomic and supermatrix approaches, and a time-calibrated phylogeny for squamate reptiles (lizards and snakes) based on 52 genes and 4162 species. Mol. Phylogenet. Evol. 2016, 94, 537–547. [Google Scholar] [CrossRef] [PubMed]
  6. Beçak, W.; Beçak, M.L. Cytotaxonomy and chromosomal evolution in Serpentes. Cytogenet. Genome Res. 1969, 8, 247–262. [Google Scholar] [CrossRef]
  7. Olmo, E.; Signorino, G.G. Chromorep: A Reptile Chromosomes Database. 2005. Available online: http://chromorep.univpm.it (accessed on 20 June 2020).
  8. Oguiura, N.; Ferrarezzi, H.; Batistic, R.F. Cytogenetics and molecular data in snakes: A phylogenetic approach. Cytogenet. Genome Res. 2009, 127, 128–142. [Google Scholar] [CrossRef]
  9. Valenzuela, N.; Lance, V.A. Temperature-Dependent Sex Determination in Vertebrates; Smithsonian Books: Washington, DC, USA, 2004; pp. 1–194. [Google Scholar]
  10. Singh, L.; Sharma, T.; Ray-Chaudhuri, S.P. Multiple sex-chromosomes in the common Indian Krait, Bungarus caeruleus Schneider. Chromosoma 1970, 31, 386–391. [Google Scholar] [CrossRef]
  11. Singh, L. Evolution of karyotypes in snakes. Chromosoma 1972, 38, 185–236. [Google Scholar] [CrossRef]
  12. Singh, L. Multiple W chromosome in a sea snake, Enhydrina schistosa Daudin. Experientia 1972, 28, 95–97. [Google Scholar] [CrossRef]
  13. Mengden, G.A.; Stock, A.D. Chromosomal evolution in Serpentes; a comparison of G and C chromosome banding patterns of some colubrid and boid genera. Chromosoma 1980, 79, 53–64. [Google Scholar] [CrossRef]
  14. Rovatsos, M.; Vukić, J.; Lymberakis, P.; Kratochvíl, L. Evolutionary stability of sex chromosomes in snakes. Proc. R Soc. B Biol. Sci. 2015, 282, 20151992. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Augstenová, B.; Mazzoleni, S.; Kratochvíl, L.; Rovatsos, M. Evolutionary dynamics of the W chromosome in caenophidian snakes. Genes 2018, 9, 5. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Augstenová, B.; Johnson Pokorná, M.; Altmanová, M.; Frynta, D.; Rovatsos, M.; Kratochvíl, L. ZW, XY, and yet ZW: Sex chromosome evolution in snakes even more complicated. Evolution 2018, 72, 1701–1707. [Google Scholar] [CrossRef] [PubMed]
  17. Matsubara, K.; Kumazawa, Y.; Ota, H.; Nishida, C.; Matsuda, Y. Karyotype analysis of four blind snake species (Reptilia: Squamata: Scolecophidia) and karyotypic changes in Serpentes. Cytogenet. Genome Res. 2019, 157, 98–106. [Google Scholar] [CrossRef]
  18. Beçak, W.; Beçak, M.L.; Nazareth, H.R.S.; Ohno, S. Close karyological kinship between the reptilian suborder Serpentes and the class Aves. Chromosoma 1964, 15, 606–617. [Google Scholar] [CrossRef]
  19. Mengden, G.A. Chromosomal Evolution and the Phylogeny of Elapid Snakes. Ph.D. Thesis, Australian National University, Canberra, Australia, 1982. [Google Scholar]
  20. Matsubara, K.; Tarui, H.; Toriba, M.; Yamada, K.; Nishida-Umehara, C.; Agata, K.; Matsuda, Y. Evidence for different origin of sex chromosomes in snakes, birds, and mammals and step-wise differentiation of snake sex chromosomes. Proc. Natl. Acad. Sci. USA 2006, 103, 18190–18195. [Google Scholar] [CrossRef] [Green Version]
  21. Mezzasalma, M.; Andreone, F.; Glaw, F.; Petraccioli, A.; Odierna, G.; Guarino, F.M. A karyological study of three typhlopid species with some inferences on chromosome evolution in blindsnakes (Scolecophidia). Zool. Anz. 2016, 264, 34–40. [Google Scholar] [CrossRef]
  22. Viana, P.F.; Ribeiro, L.B.; Souza, G.M.; Chalkidis, H.M.; Gross, M.C.; Feldberg, E. Is the karyotype of neotropical boid snakes really conserved? Cytotaxonomy, chromosomal rearrangements and karyotype organization in the Boidae family. PLoS ONE 2016, 11, e0160274. [Google Scholar] [CrossRef]
  23. Augstenová, B.; Mazzoleni, S.; Kostmann, A.; Altmanová, M.; Frynta, D.; Kratochvíl, L.; Rovatsos, M. Cytogenetic analysis did not reveal differentiated sex chromosomes in ten species of boas and pythons (Reptilia: Serpentes). Genes 2019, 10, 934. [Google Scholar] [CrossRef] [Green Version]
  24. Vicoso, B.; Emerson, J.J.; Zektser, Y.; Mahajan, S.; Bachtrog, D. Comparative sex chromosome genomics in snakes: Differentiation, evolutionary strata, and lack of global dosage compensation. PLoS Biol. 2013, 11, e1001643. [Google Scholar] [CrossRef] [Green Version]
  25. Ohno, S. Sex. Chromosomes and Sex-Linked Genes; Springer: Berlin, Germany, 1967; pp. 1–167. [Google Scholar]
  26. Booth, W.; Johnson, D.H.; Moore, S.; Schal, C.; Vargo, E.L. Evidence for viable, non-clonal but fatherless Boa constrictors. Biol. Lett. 2011, 7, 253–256. [Google Scholar] [CrossRef] [PubMed]
  27. Gamble, T.; Castoe, T.A.; Nielsen, S.V.; Banks, J.L.; Card, D.C.; Schield, D.R.; Schuett, G.W.; Booth, W. The discovery of XY sex chromosomes in a boa and python. Curr. Biol. 2017, 27, 2148–2153.e4. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Rovatsos, M.; Kratochvíl, L.; Altmanová, M.; Johnson Pokorná, M. Interstitial telomeric motifs in squamate reptiles: When the exceptions outnumber the rule. PLoS ONE 2015, 10, e0134985. [Google Scholar] [CrossRef] [Green Version]
  29. O’Meally, D.; Patel, H.R.; Stiglec, R.; Sarre, S.D.; Georges, A.; Graves, J.A.M.; Ezaz, T. Non-homologous sex chromosomes of birds and snakes share repetitive sequences. Chromosome Res. 2010, 18, 787–800. [Google Scholar] [CrossRef]
  30. Literman, R.; Badenhorst, D.; Valenzuela, N. qPCR-based molecular sexing by copy number variation in rRNA genes and its utility for sex identification in soft-shell turtles. Methods Ecol. Evol. 2014, 5, 872–880. [Google Scholar] [CrossRef] [Green Version]
  31. Lee, L.; Montiel, E.E.; Valenzuela, N. Discovery of putative XX/XY male heterogamety in Emydura subglobosa turtles exposes a novel trajectory of sex chromosome evolution in Emydura. Cytogenet. Genome Res. 2019, 158, 160–169. [Google Scholar] [CrossRef]
  32. Singchat, W.; Kraichak, E.; Tawichasri, P.; Tawan, T.; Suntronpong, A.; Sillapaprayoon, S.; Phatcharakullawarawat, R.; Muangmai, N.; Suntrarachun, S.; Baicharoen, S.; et al. Dynamics of telomere length in captive Siamese cobra (Naja kaouthia) related to age and sex. Ecol. Evol. 2019, 9, 6366–6377. [Google Scholar] [CrossRef] [Green Version]
  33. Mazzoleni, S.; Augstenová, B.; Clemente, L.; Auer, M.; Fritz, U.; Praschag, P.; Protiva, T.; Velenský, P.; Kratochvíl, L.; Rovatsos, M. Sex is determined by XX/XY sex chromosomes in Australasian side-necked turtles (Testudines: Chelidae). Sci. Rep. 2020, 10, 4276. [Google Scholar] [CrossRef] [Green Version]
  34. Rovatsos, M.; Johnson Pokorná, M.; Altmanová, M.; Kratochvíl, L. Female heterogamety in Madagascar chameleons (Squamata: Chamaeleonidae: Furcifer): Differentiation of sex and neo-sex chromosomes. Sci. Rep. 2015, 5, 13196. [Google Scholar] [CrossRef] [Green Version]
  35. Nagy, Z.T.; Sonet, G.; Glaw, F.; Vences, M. First large-scale DNA barcoding assessment of reptiles in the biodiversity hotspot of Madagascar, based on newly designed COI primers. PLoS ONE 2012, 7, e34506. [Google Scholar] [CrossRef]
  36. Burbrink, F.T.; Lawson, R.; Slowinski, J.B. Mitochondrial DNA phylogeography of the polytypic North American rat snake (Elaphe obsoleta): A critique of the subspecies concept. Evolution 2000, 54, 2107–2118. [Google Scholar] [CrossRef] [PubMed]
  37. de Queiroz, A.; Lawson, R.; Lemos-Espinal, J.A. Phylogenetic relationships of North American garter snakes (Thamnophis) based on four mitochondrial genes: How much DNA sequence is enough? Mol. Phyl. Evol. 2002, 22, 315–329. [Google Scholar] [CrossRef] [PubMed]
  38. Koubová, M.; Johnson Pokorná, M.; Rovatsos, M.; Farkačová, K.; Altmanová, M.; Kratochvíl, L. Sex determination in Madagascar geckos of the genus Paroedura (Squamata: Gekkonidae): Are differentiated sex chromosomes indeed so evolutionary stable? Chromosome Res. 2014, 22, 441–452. [Google Scholar] [CrossRef]
  39. Mazzoleni, S.; Augstenová, B.; Clemente, L.; Auer, M.; Fritz, U.; Praschag, P.; Protiva, T.; Velenský, P.; Kratochvíl, L.; Rovatsos, M. Turtles of the genera Geoemyda and Pangshura (Testudines: Geoemydidae) lack differentiated sex chromosomes: The end of a 40-year error cascade for Pangshura. PeerJ 2019, 7, e6241. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Altschul, S.F.; Gish, W.; Miller, W.; Myers, E.W.; Lipman, D.J. Basic local alignment search tool. J. Mol. Biol. 1990, 215, 403–410. [Google Scholar] [CrossRef]
  41. Sumner, A.T. A simple technique for demonstrating centromeric heterochromatin. Exp. Cell Res. 1972, 75, 304–306. [Google Scholar] [CrossRef]
  42. Ijdo, J.W.; Baldini, A.; Ward, D.C.; Reeders, S.T.; Wells, R.A. Origin of human chromosome 2: An ancestral telomere-telomere fusion. Proc. Natl. Acad. Sci. USA 1991, 88, 9051–9055. [Google Scholar] [CrossRef] [Green Version]
  43. Endow, S.A. Polytenization of the ribosomal genes on the X and Y chromosomes of Drosophila melanogaster. Genetics 1982, 100, 375–385. [Google Scholar] [CrossRef]
  44. Rovatsos, M.; Altmanová, M.; Augstenová, B.; Mazzoleni, S.; Velenský, P.; Kratochvíl, L. ZZ/ZW sex determination with multiple neo-sex chromosomes is common in Madagascan chameleons of the genus Furcifer (Reptilia: Chamaeleonidae). Genes 2019, 10, 1020. [Google Scholar] [CrossRef] [Green Version]
  45. Gorman, G.C.; Gress, F. Chromosome cytology of four boid snakes and a varanid lizard, with comments on the cytosystematics of primitive snakes. Herpetologica 1970, 26, 308–317. [Google Scholar]
  46. Sharma, O.P.; Kour, G. On the Chromosomes of four species of Indian snakes. Cytologia 2005, 70, 65–70. [Google Scholar] [CrossRef] [Green Version]
  47. Singh, L.; Sharma, T.; Ray-Chaudhuri, S. Chromosomes and the classification of the snakes of the family Boidae. Cytogenet. Genome Res. 1968, 7, 161–168. [Google Scholar] [CrossRef] [PubMed]
  48. Beçak, W.; Beçak, M.L. W-sex chromatin fluorescence in snakes. Experientia 1972, 28, 228–229. [Google Scholar] [CrossRef] [PubMed]
  49. Heneen, W.K.; Habib, Z.A.; Röhme, D. Heteromorphism of constitutive heterochromatin in carcinoma and dysplasia of the uterine cervix. Eur. J. Obstet. Gynecol. 1980, 10, 173–182. [Google Scholar] [CrossRef]
  50. Freitas, L.; Seuánez, H. Chromosome heteromorphisms in Cebus apella. J. Hum. Evol. 1982, 11, 173–180. [Google Scholar] [CrossRef]
  51. Haaf, T.; Schmid, M. Chromosome heteromorphisms in the gorilla karyotype: Analyses with distamycin A/DAPI, quinacrine and 5-azacytidine. Heredity 1987, 78, 287–292. [Google Scholar] [CrossRef]
  52. Bressa, M.J.; Franco, M.J.; Toscani, M.A.; Papeschi, A.G. Heterochromatin heteromorphism in Holhymenia rubiginosa (Heteroptera: Coreidae). Eur. J. Entomol. 2008, 105, 65–72. [Google Scholar] [CrossRef] [Green Version]
  53. Ferreira, G.; Barbosa, L.M.; Prizon-Nakajima, A.C.; de Paiva, S.; Vieira, M.; Gallo, R.B.; Borin-Carvalho, L.A.; da Rosa, R.; Wadzki, C.; Dos Santos, I.; et al. Constitutive heterochromatin heteromorphism in the Neotropical armored catfish Hypostomus regain (Ihering, 1905) (Loricariidae, Hypostominae) from the Paraguay River basin (Mato Grosso do Sul, Brazil). Comp. Cytogenet. 2019, 13, 27–39. [Google Scholar] [CrossRef] [Green Version]
  54. Sims, S.H.; Macgregor, H.C.; Pellatt, P.S.; Horner, H.A. Chromosome 1 in crested and marbled newts (Triturus). Chromosoma 1984, 89, 169–185. [Google Scholar] [CrossRef]
  55. Mezzasalma, M.; Andreone, F.; Aprea, G.; Glaw, F.; Odierna, G.; Guarino, F.M. When can chromosomes drive speciation? The peculiar case of the Malagasy tomato frogs (genus Dyscophus). Zool. Anz. 2017, 268, 41–46. [Google Scholar] [CrossRef]
  56. Batistic, R.F.; Ferrarezzi, H.; Soma, M. O cariótipo de Tropidophis paucisquamis e suas afinidades com outras famílias. Resumos do III Simpósio do Programa Biota/FAPESP Universidade Federal de São Carlos. 2002. Available online: https://www.biota.org.br/publi/banco/index?show+91144174 (accessed on 15 May 2022).
  57. Mezzasalma, M.; Andreone, F.; Branch, W.R.; Glaw, F.; Guarino, F.M.; Nagy, Z.T.; Odierna, G.; Aprea, G. Chromosome evolution in pseudoxyrhophiine snakes from Madagascar: A wide range of karyotypic variability. Biol. J. Linn. Soc. 2014, 112, 450–460. [Google Scholar] [CrossRef]
  58. Porter, C.A.; Hamilton, M.J.; Sites, J.W., Jr.; Baker, R.J. Location of ribosomal DNA in chromosomes of squamate reptiles: Systematic and evolutionary implications. Herpetologica 1991, 47, 271–280. [Google Scholar]
  59. Porter, C.; Haiduk, M.; De Queiroz, K. Evolution and Phylogenetic significance of ribosomal gene location in chromosomes of squamate reptiles. Copeia 1994, 1994, 302–313. [Google Scholar] [CrossRef]
  60. Viana, P.F.; Ezaz, T.; de Bello Cioffi, M.; Jackson Almeida, B.; Feldberg, E. Evolutionary insights of the ZW sex chromosomes in snakes: A new chapter added by the amazonian puffing snakes of the genus Spilotes. Genes 2019, 10, 288. [Google Scholar] [CrossRef] [Green Version]
  61. Hernando, A.; García, J.A. Standard karyotype and nucleolus organizer region of Neotropical blindsnake Typhlops brongersmianus, Serpentes: Typhlopidae. Acta Herpetol. 2007, 2, 117–120. [Google Scholar]
  62. Bruschi, D.; Rivera, M.; Lima, A.; Zúñiga, A.; Recco-Pimentel, S. Interstitial Telomeric Sequences (ITS) and major rDNA mapping reveal insights into the karyotypical evolution of Neotropical leaf frogs species (Phyllomedusa, Hylidae, Anura). Mol. Cytogenet. 2014, 7, 22. [Google Scholar] [CrossRef] [Green Version]
  63. Augstenová, B.; Pensabene, E.; Kratochvíl, L.; Rovatsos, M. Cytogenetic evidence for sex chromosomes and karyotype evolution in anguimorphan lizards. Cells 2021, 10, 1612. [Google Scholar] [CrossRef]
  64. Clemente, L.; Mazzoleni, S.; Pensabene Bellavia, E.; Augstenová, B.; Auer, M.; Praschag, P.; Protiva, T.; Velenský, P.; Wagner, P.; Fritz, U.; et al. Interstitial telomeric repeats are rare in turtles. Genes 2020, 11, 657. [Google Scholar] [CrossRef]
  65. Camper, J.; Hanks, B. Variation in the nucleolus organizer region among New World snakes. J. Herpetol. 1995, 29, 468–471. [Google Scholar] [CrossRef]
  66. Rovatsos, M.; Pokorná, M.J.; Kratochvíl, L. Differentiation of sex chromosomes and karyotype characterisation in the dragon snake Xenodermus javanicus (Squamata: Xenodermatidae). Cytogenet. Genome Res. 2015, 147, 48–54. [Google Scholar] [CrossRef]
  67. Backström, N.; Forstmeier, W.; Schielzeth, H.; Mellenius, H.; Nam, K.; Bolund, E.; Webster, M.T.; Öst, T.; Schneider, M.; Kempenaers, B.; et al. The recombination landscape of the zebra finch Taeniopygia guttata genome. Genome Res. 2010, 20, 485–495. [Google Scholar] [CrossRef] [Green Version]
  68. Groenen, M.A.M.; Wahlberg, P.; Foglio, M.; Cheng, H.H.; Megens, H.J.; Crooijmans, R.P.M.A.; Besnier, F.; Lathrop, M.; Muir, W.M.; Wong, G.K.; et al. A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate. Genome Res. 2009, 19, 510–519. [Google Scholar] [CrossRef] [Green Version]
  69. Schield, D.R.; Pasquesi, G.I.M.; Perry, B.W.; Adams, R.H.; Nikolakis, Z.L.; Westfall, A.K.; Orton, R.W.; Meik, J.M.; MacKessy, S.P.; Castoe, T.A.; et al. Snake recombination landscapes are concentrated in functional regions despite PRDM9. Mol. Biol. Evol. 2020, 37, 1272–1294. [Google Scholar] [CrossRef]
  70. Azzalin, C.M.; Nergadze, S.G.; Giulotto, E. Human intrachromosomal telomeric-like repeats: Sequence organization and mechanisms of origin. Chromosoma 2001, 110, 75–82. [Google Scholar] [CrossRef]
  71. Mallery, C.S., Jr.; Carrillo, M.M. A case study of sex-linkage in Python regius (Serpentes: Boidae), with new insights into sex determination in Henophidia. Phyllomedusa 2016, 15, 29–42. [Google Scholar] [CrossRef] [Green Version]
  72. Booth, W.; Schuett, G.W.; Ridgway, A.; Buxton, D.W.; Castoe, T.A.; Bastone, G.; Bennett, C.; McMahan, W. New insights on facultative parthenogenesis in pythons. Biol. J. Linn. Soc. 2014, 112, 461–468. [Google Scholar] [CrossRef]
  73. Kratochvíl, L.; Stöck, M.; Rovatsos, M.; Bullejos, M.; Herpin, A.; Jeffries, D.L.; Peichel, C.L.; Perrin, N.; Valenzuela, N.; Pokorná, M.J. Expanding the classical paradigm: What we have learnt from vertebrates about sex chromosome evolution. Phil. Trans. R. Soc. B 2021, 376, 20200097. [Google Scholar] [CrossRef]
  74. Gamble, T.; Coryell, J.; Ezaz, T.; Lynch, J.; Scantlebury, D.P.; Zarkower, D. Restriction site-associated DNA sequencing (RAD-seq) reveals an extraordinary number of transitions among gecko sex-determining systems. Mol. Biol. Evol. 2015, 32, 1296–1309. [Google Scholar] [CrossRef] [Green Version]
  75. Keating, S.E.; Blumer, M.; Grismer, L.L.; Lin, A.; Nielsen, S.V.; Thura, M.K.; Wood, P.L., Jr.; Quah, E.S.H.; Gamble, T. Sex chromosome turnover in bent-toed geckos (Cyrtodactylus). Genes 2021, 12, 116. [Google Scholar] [CrossRef]
  76. Kostmann, A.; Augstenová, B.; Frynta, D.; Kratochvíl, L.; Rovatsos, M. Cytogenetically elusive sex chromosomes in scincoidean lizards. Int. J. Mol. Sci. 2021, 22, 8670. [Google Scholar] [CrossRef]
Figure 1. Giemsa-stained karyograms are depicted for the species: (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus. Sex is indicated.
Figure 1. Giemsa-stained karyograms are depicted for the species: (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus. Sex is indicated.
Genes 13 01185 g001
Figure 2. C-banded metaphases for the species: (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus. Chromosomes with polymorphism in heterochromatic blocks are indicated by arrowheads. Sex is indicated.
Figure 2. C-banded metaphases for the species: (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus. Chromosomes with polymorphism in heterochromatic blocks are indicated by arrowheads. Sex is indicated.
Genes 13 01185 g002
Figure 3. The distribution of telomeric repeats (TTAGGG)n in metaphases. (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus. Chromosomes with ITRs are marked with arrowheads. Sex is indicated.
Figure 3. The distribution of telomeric repeats (TTAGGG)n in metaphases. (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus. Chromosomes with ITRs are marked with arrowheads. Sex is indicated.
Genes 13 01185 g003
Figure 4. The distribution of rDNA loci in metaphases for the species: (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus, marked with arrowheads. Sex is indicated.
Figure 4. The distribution of rDNA loci in metaphases for the species: (a,b) Eryx colubrinus, (c,d) Eryx conicus, (e,f) Eryx miliaris, (g,h) Eryx muelleri, (i,j) Python regius, (k) Cylindrophis ruffus, and (l) Tropidophis melanurus, marked with arrowheads. Sex is indicated.
Genes 13 01185 g004
Figure 5. Comparative genome hybridization in metaphases for the species: (ad) Eryx colubrinus, (eh) Eryx conicus, (il) Eryx miliaris, (mp) Eryx muelleri, and (qt) Python regius. Sex-specific regions were not identified in any of the studied specimens. For each metaphase, we present an image of the merged signal from the hybridization of the green (male-specific) and red (female-specific) probe and a photo with DAPI stain to better visualize the chromosome morphology. Sex is indicated.
Figure 5. Comparative genome hybridization in metaphases for the species: (ad) Eryx colubrinus, (eh) Eryx conicus, (il) Eryx miliaris, (mp) Eryx muelleri, and (qt) Python regius. Sex-specific regions were not identified in any of the studied specimens. For each metaphase, we present an image of the merged signal from the hybridization of the green (male-specific) and red (female-specific) probe and a photo with DAPI stain to better visualize the chromosome morphology. Sex is indicated.
Genes 13 01185 g005
Table 1. List of examined specimens.
Table 1. List of examined specimens.
FamilySpeciesSex
CylindrophiidaeCylindrophis ruffus01
ErycidaeEryx colubrinus22
Eryx conicus11
Eryx miliaris33
Eryx muelleri11
PythonidaePython regius34
TropidophiidaeTropidophis melanurus01
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Charvát, T.; Augstenová, B.; Frynta, D.; Kratochvíl, L.; Rovatsos, M. Cytogenetic Analysis of the Members of the Snake Genera Cylindrophis, Eryx, Python, and Tropidophis. Genes 2022, 13, 1185. https://doi.org/10.3390/genes13071185

AMA Style

Charvát T, Augstenová B, Frynta D, Kratochvíl L, Rovatsos M. Cytogenetic Analysis of the Members of the Snake Genera Cylindrophis, Eryx, Python, and Tropidophis. Genes. 2022; 13(7):1185. https://doi.org/10.3390/genes13071185

Chicago/Turabian Style

Charvát, Tomáš, Barbora Augstenová, Daniel Frynta, Lukáš Kratochvíl, and Michail Rovatsos. 2022. "Cytogenetic Analysis of the Members of the Snake Genera Cylindrophis, Eryx, Python, and Tropidophis" Genes 13, no. 7: 1185. https://doi.org/10.3390/genes13071185

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop