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DNApol ‐ϵ gene is indispensable for the survival and growth of Drosophila melanogaster
Author(s) -
Verma Akanksha,
Sengupta Sonali,
Lakhotia Subhash C.
Publication year - 2012
Publication title -
genesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.093
H-Index - 110
eISSN - 1526-968X
pISSN - 1526-954X
DOI - 10.1002/dvg.20791
Subject(s) - biology , drosophila melanogaster , imaginal disc , genetics , mutant , gene , transgene , complementation , allele , exon , drosophilidae , somatic cell , melanogaster , intron , mutation , microbiology and biotechnology
Based on deletion and complementation mapping and DNA sequencing, a new recessive fully penetrant mutation ( DNApol ‐ϵ pl10R ), causing prolonged larval life and larval/early pupal lethality, is identified as the first mutant allele of the DNApol ‐ϵ ( CG6768 ) gene of Drosophila melanogaster . A same‐sense base pair substitution in exon 1 of the DNApol ‐ϵ gene is associated with retention of the first intron and significant reduction in DNApol‐ϵ transcripts in DNApol ‐ϵ pl10R homozygotes. Homozygous mutant larvae show small imaginal discs with fewer cells and reduced polyteny in salivary glands, presumably because of the compromised DNA polymerase function following exhaustion of the maternal contribution. Extremely small and rare DNApol ‐ϵ pl10R homozygous somatic clones in DNApol ‐ϵ pl10R /+ imaginal discs confirm their poor mitotic activity. The DNApol ‐ϵ pl10R homozygotes, like those expressing DNApol‐ϵ‐RNAi transgene, show high sensitivity to DNA damaging agents. The first mutant allele of the DNApol ‐ϵ gene will facilitate functional characterization of this enzyme in the genetically tractable Drosophila model. genesis 50:86–101, 2012. © 2011 Wiley Periodicals, Inc.