The Drosophila Mutagen-Sensitivity Gene mus109 Encodes DmDNA2

Abstract

The identification of mutants through forward genetic screens is the backbone of Drosophila genetics research, yet many mutants identified through these screens have yet to be mapped to the Drosophila genome. This is especially true of mutants that have been identified as mutagen-sensitive (mus), but have not yet been mapped to their associated molecular locus. Our study addressed the need for additional mus gene identification by determining the locus and exploring the function of the X-linked mutagen-sensitive gene mus109 using three available mutant alleles: mus109^D1, mus109^D2, and mus109^lS. After first confirming that all three mus109 alleles were sensitive to methyl methanesulfonate (MMS) using complementation analysis, we used deletion mapping to narrow the candidate genes for mus109. Through DNA sequencing, we were able to determine that mus109 is the uncharacterized gene CG2990, which encodes the Drosophila ortholog of the highly conserved DNA2 protein that is important for DNA replication and repair. We further used the sequence and structure of DNA2 to predict the impact of the mus109 allele mutations on the final gene product. Together, these results provide a tool for researchers to further investigate the role of DNA2 in DNA repair processes in Drosophila.

1. Introduction

The development of gene mapping techniques has a long and storied history in the Drosophila melanogaster model system (reviewed in [1]), beginning with Alfred Sturtevant’s fundamental publication of the first genetic map in 1913 [2]. In this work, Sturtevant showed that genes are arranged in a linear order along chromosomes and that the recombination frequency between two genes could be used as a measure of the distance between them. This discovery created the foundation for other key advances in Drosophila gene mapping, including the generation of detailed polytene chromosome cytogenetic maps [3,4], the development of deletion kits covering the genome [5,6,7], and the sequencing of the D. melanogaster genome [8].

However, despite these advances, the current D. melanogaster genome annotation includes 14,184 genes that have not yet been mapped to the molecular genome (FlyBase R6.43; [9]), including many genes that were discovered in forward genetic screens. In these cases, alleles have been discovered that produce a phenotype of interest, but the molecular locus responsible for this phenotype remains unknown. For example, several forward genetic screens have been conducted to identify D. melanogaster mutants with defects in DNA repair (e.g., [10,11,12,13,14,15]). In these screens, flies that showed reduced survival in the presence of a mutagen—usually the alkylating agent methyl methanesulfonate (MMS)—were identified as probable DNA repair mutants. To date, 58 of these mutagen-sensitive (mus) stocks have been generated, yet the gene responsible for the mus phenotype is known for only 15 of these stocks [16,17]. Importantly, each mapped mus gene has encoded an ortholog of a human DNA repair protein [17], including proteins implicated in disorders such as Bloom syndrome [18], Fanconi anemia [16], and xeroderma pigmentosum [19].

The knowledge derived from studies of these 15 mapped mus genes demonstrates the utility of mapping mus genes to facilitate DNA repair research in Drosophila. With this in mind, we sought to map mus109, an X-linked essential gene with three extant alleles: mus109^D1 [13] and mus109^D2 [14] are homozygous viable hypomorphic alleles, whereas mus109^lS is a homozygous lethal null allele [20]. mus109 mutants are characterized by chromosomal instability in the absence of mutagen treatment [20,21,22,23], with the majority of chromosome breaks occurring in heterochromatin [22]. Further, mus109 mutants are sensitive to MMS, 4-nitroquinoline-1-oxide (4NQO), and γ irradiation [13,14,24,25], which are mutagens that create DNA adducts (MMS and 4NQO; [26,27]) and oxidative damage (γ irradiation; [28]). In this manuscript, we present detailed mapping data obtained through complementation analysis, deletion crosses, and DNA sequence alignment showing that mus109 is the uncharacterized Drosophila gene CG2990 (human DNA2). We further discuss the potential functionality of the mus109 mutant alleles by comparing the mutations to conserved catalytic regions in DNA2.

2. Materials and Methods

2.1. Drosophila Stocks and Maintenance

D. melanogaster stocks were maintained at 25 °C in bottles containing Nutri-Fly Bloomington Formulation media (Genesee Scientific) with a 12h day/night cycle. Experimental crosses were conducted in narrow vials containing corn syrup/soy media (Archon Scientific). The following fly stocks were obtained from the Bloomington Drosophila Stock Center (BDSC): mus109^D1 (BDSC# 2320), mus109^D2 (BDSC# 2307), mus109^lS (BDSC# 4168), Df(1)ED6991 (BDSC# 37535), Df(1)ED6989 (BDSC# 9056), Df(1)BSC539 (BDSC# 25067), Df(1)BSC754 (BDSC# 26852), DGRP-59 (wild-type; BDSC# 28129), and FM7c, P{GAL4-Kr.C}DC1, P{UAS-GFP.S65T}DC5, sn⁺ (BDSC# 5193).

2.2. Complementation Analysis

Five mus109 heterozygous females—carrying either the mus109^D1, mus109^D2, or mus109^lS chromosome over an X chromosome balancer marked with the dominant Bar eye phenotype—were crossed to five hemizygous mus109^D1 or mus109^D2 males per vial to establish Brood 1 (day 0). On day 3, the flies were flipped into new vials to establish Brood 2. On day 4, Brood 1 vials were mock treated with 250 µL water. On day 5, the adult flies were discarded from Brood 2 vials, and on day 6, Brood 2 vials were treated with 250 µL 0.05% methyl methanesulfonate (MMS; Sigma-Aldrich). Adult offspring were frozen on day 18 (Brood 1) or day 21 (Brood 2) and were subsequently scored for sex and eye phenotype. For each vial, relative survival was calculated as the ratio of mus109 mutant to non-mutant flies in Brood 2, normalized to the same ratio in the corresponding Brood 1 vial. Vials with fewer than 15 progeny in either Brood 1 or 2 were excluded from analysis, as in [29]. Statistical significance was determined by one-way ANOVA with Tukey’s correction for multiple comparisons. Statistical analysis and graphing were performed using GraphPad Prism 7.05.

2.3. Deletion Mapping

Four deletions covering the area predicted by Mason et al. [14] to contain mus109 were selected: Df(1)ED6991, Df(1)ED6989, Df(1)BSC539, and Df(1)BSC754. Five heterozygous females—carrying one of the deletions over an X chromosome balancer—were crossed to five mus109^D2 males per vial to establish Brood 1 (day 0). The remainder of the MMS sensitivity assay proceeded as in the complementation analysis crosses.

2.4. DNA Sequencing

For the mus109^D1 and mus109^D2 alleles, DNA was extracted from single adult hemizygous males using the protocol described in [30]. For mus109^lS, flies were balanced with the FM7c, P{GAL4-Kr.C}DC1, P{UAS-GFP.S65T}DC5, sn⁺ chromosome and homozygous third-instar larvae were identified by the absence of green fluorescence. DNA was then extracted from single homozygous third-instar larvae using the same protocol described in [30]. From these extracts, the CG2990 coding region was amplified, purified with a GeneJet Gel Extraction Kit (Thermo Scientific), and sequenced (Eurofins Genomics). The primers used in PCR and sequencing are shown in Table S1. Sequences were aligned to the FlyBase [31] CG2990 reference sequence and identified mutations were confirmed on a second DNA sample.

2.5. Protein Alignment

Clustal Omega [32] was used to conduct amino acid sequence alignment between DNA2 orthologs in wild-type D. melanogaster (NCBI Accession# NP_727386), Mus musculus (NCBI Accession# NP_796346.2), Homo sapiens (NCBI Accession# NP_001073918.2), and Caenorhabditis elegans (NCBI Accession# NP_496516.1). Alignment was visualized using Jalview version 2.11.1.4 [33]. Domains were mapped and analyzed according to the domain map devised by Zhou et al. [34] based on the structure of M. musculus DNA2.

3. Results and Discussion

Since the three mus109 alleles—mus109^D1, mus109^D2, and mus109^lS—were identified in the early 1980s [14,20,24], we first used complementation analysis to confirm that the fly stocks were still mutagen-sensitive. All possible mus109 allelic combinations showed sensitivity to MMS with significantly lower relative survival values compared to wild-type (one-way ANOVA, F(5,50) = 255.7, p < 0.0001; Figure 1). Although the relative survival values were not significantly different between the mus109 allele combinations (p = 0.221), the relative survival values were lower in genotypes containing mus109^lS than in combinations without mus109^lS (Figure S1), consistent with previous suggestions that mus109^lS is amorphic [20] whereas mus109^D1 and mus109^D2 are hypomorphic [21].

Next, deletion mapping was used to narrow the genomic location of mus109. Four deletions spanning the approximately 630 kb region predicted to contain mus109 [14] were each crossed to mus109^D2 and assayed for sensitivity to MMS. With relative survival values of 0 in each case (Table S2), all four deletions failed to complement mus109^D2. Thus, the location of mus109 was narrowed to the approximately 62kb region shared by all deletions (Figure 2). The FlyBase entries for the nine genes within this region were reviewed to identify genes involved in DNA metabolism (

Table 1. Predicted function of genes within mus109^D2 and the non-complementing region.

Gene	Summary *
asRNA:CR45185	Antisense long non-coding RNA; function unknown.
asRNA:CR45601	Antisense long non-coding RNA; function unknown.
CG2990	5′-3′ DNA helicase, 5′-flap endonuclease; orthologous to HsDNA2 (DNA replication helicase/nuclease 2).
CG15312	Function unknown.
CG33557	DNA-binding transcription factor; orthologous to HsSCX (scleraxis bHLH transcription factor).
Cht6	Chitinase; orthologous to HsCHIT1 (chitinase 1).
Gr9a	Gustatory receptor.
Yp1	Yolk protein.
Yp2	Yolk protein.

* Information derived from gene ontology, summaries, and human orthologs sections of each gene’s FlyBase entry.

), a characteristic of all mapped mus genes. Notably, one of these genes, CG2990, is orthologous to the well-characterized DNA repair gene DNA2 [17]. Similar to Drosophila mus109, DNA2 is essential in yeast and mice [35,36], its downregulation causes genome instability in yeast and human cells [37,38], and yeast Dna2 mutants are sensitive to MMS [39]. Collectively, these observations suggested that CG2990 is an ideal mus109 candidate gene. To test our hypothesis that mus109 was CG2990, we sequenced the CG2990 coding region in wild-type flies and in each of the three mus109 alleles. In comparing these sequences, we identified mutations resulting in premature stop codons in all three mus109 alleles as well as eight missense mutations in mus109^D1 (Figure 3A), all of which likely affect the functionality of the mus109 gene product.

The DNA2 protein is an essential and conserved nuclease-helicase with roles in several pathways that are crucial for maintaining genome integrity (reviewed in [41]). These pathways include long-track end resection during homologous recombination [42], Okazaki fragment processing [43], the recovery of stalled replication forks [44], and the maintenance of mitochondrial DNA [45]. Underscoring the importance of this protein, human DNA2 mutations have been implicated in mitochondrial myopathy [46], microcephalic primordial dwarfism [47], and some cancers [48]. DNA2 consists of a structure-specific nuclease and helicase/DNA-dependent ATPase connected by a β-barrel stalk [34]. While the nuclease activity is most critical to DNA2 repair functions [49,50,51], the helicase domains contribute to the narrow tunnel-like structure of DNA2 that allows single-stranded DNA access to the nuclease [34].

To explore the possible impact of the nonsense and missense mutations on mus109 mutant allele functionality, we mapped DNA2 domains onto CG2990 using the mouse DNA2 protein structure [34] (Figure 3B). Like mouse DNA2, CG2990 contains a structure-specific nuclease domain and a helicase/DNA-dependent ATPase domain connected by a β-barrel stalk sequence, as well as two helicase motifs (1A and 2A) [34]. The two helicase motifs are common to members of the Upf1 subfamily of helicases and contain an ATPase at their cleft [52]; however, helicase and ATPase activity are considered weak and non-essential to DNA2 nuclease function [34,49].

We further compared the CG2990 and human DNA2 protein sequences. The amino acid sequence alignment of CG2990 confirmed sequence homology to human DNA2 as well as with other model species (Figure 4). CG2990 contains the highly conserved DEXXQ-box helicase motif, as well as all known active site residues as defined in Zhou et al. [34]. Similarly, CG2990 contains most of the DNA contact site residues found in mouse DNA2 [34]. The insertion/deletion mutation in mus109^lS creates a premature stop codon prior to the active site residues in the nuclease domain. This mutation likely abolishes nuclease function, which is known to be essential for viability in yeast [49]. If so, this could explain the homozygous lethal phenotype of mus109^lS mutants. In contrast, the nonsense mutations in the mus109^D1 and mus109^D2 alleles occur after the conserved nuclease domain, which may allow for functional nuclease activity. While the nonsense mutation in mus109^D1 occurs in the second helicase domain, the I663V mutation in the stalk domain changes a highly conserved amino acid (Figure 4), which may impact protein folding and/or helicase functionality.

Considering our deletion mapping data and our identification of deleterious mutations in CG2990, we conclude that mus109 is CG2990, the Drosophila ortholog of DNA2 [17]. This knowledge will be immediately useful to the DNA repair community, as there are no existing non-transgenic alleles of CG2990. With the identification of three (two hypomorphic and one amorphic) alleles of CG2990, future genetic studies on the functions of DmDNA2 in DNA repair can be conducted. For example, comparisons between the mus109^D1 and mus109^D2 alleles exposed to mutagens that impact DNA replication could be used to dissect the function of the DmDNA2 helicase 1A domain, which is present in mus109^D1 but not mus109^D2. Likewise, investigations of the mus109^D1 allele may further uncover the importance of the DmDNA2 helicase 2A domain, as this domain is not predicted to contribute to the tunnel structure needed for the nucleolytic activity of DNA2. Both of these genetic studies would also benefit from complementary biochemical analyses of the truncated DmDNA2 proteins produced in mus109^D1 and mus109^D2 mutants. Further, because DNA2 has been shown to act as a tumor suppressor (reviewed in [41]), the nuclease domain mutant allele may serve as a model with which to study DNA2-deficient cancer processes. Future studies may also aim to investigate genetic interactions with DmDNA2 by creating flies mutant in both DNA2 and a critical gene in a redundant double-strand break repair pathway, such as tosca (Exo1). These and other experimental possibilities will greatly contribute to the growing body of work on DNA repair mechanisms and strengthen the use of Drosophila as a model for biomedical research.