CSB-independent, XPC-dependent transcription-coupled repair in Drosophila

Author:

Deger Nazli12,Cao Xuemei1ORCID,Selby Christopher P.1,Gulec Saygin1,Kawara Hiroaki1,Dewey Evan B.2,Wang Li1,Yang Yanyan1ORCID,Archibald Sierra1,Selcuk Berkay3ORCID,Adebali Ogun3,Sekelsky Jeff2ORCID,Sancar Aziz12ORCID,Liu Zhenxing1ORCID

Affiliation:

1. Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599

2. Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599

3. Molecular Biology, Genetics, and Bioengineering Program, Faculty of Engineering and Natural Sciences, Sabanci University, 34956 Istanbul, Turkey

Abstract

Significance We have discovered that Drosophila , which does not have the canonical TCR homologs, does nevertheless carry out TCR as efficiently as organisms that do. Furthermore, using the XR-seq and in vivo excision assay we have also shown that both global repair and TCR in Drosophila are dependent on the XPC protein and in that regard, Drosophila excision repair is more similar to the monocellular eukaryotic yeast repair system than it is to multicellular eukaryotes. Finally, we have generated genome-wide single nucleotide repair maps of Drosophila for CPDs, (6-4) photoproducts, and cisplatin-d(GpG) adducts that should be a useful source for investigators working on DNA damage, repair, and mutagenesis in Drosophila .

Funder

HHS | NIH | National Institute of General Medical Sciences

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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