Comparative analyses of two primate species diverged by more than 60 million years show different rates but similar distribution of genome-wide UV repair events

Umit Akkose^1,#, Veysel Ogulcan Kaya^1,#, Laura Lindsey-Boltz^2,#, Zeynep Karagoz¹, Adam D. Brown³, Peter A. Larsen^4,†, Anne D. Yoder⁴, Aziz Sancar², Ogun Adebali^1,*

1. Molecular Biology, Genetics & Bioengineering Program, Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul, 34956, Turkey
2. Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, 27599, USA
3. Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina, 27708, USA
4. Department of Biology, Duke University, Durham, North Carolina, 27708, USA

^† Current Address: Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, 55112, USA

^# These authors contributed equally
^* To whom correspondence should be addressed: oadebali@sabanciuniv.edu

Running title: Nucleotide excision repair profiles in primates

Keywords: Nucleotide excision repair, UV damage, XR-seq, Mouse Lemur, (6-4)PP, CPD, Primate

Abstract

Nucleotide excision repair is the primary DNA repair mechanism that removes bulky DNA adducts such as UV-induced pyrimidine dimers. Correspondingly, genome-wide mapping of nucleotide excision repair with eXcision Repair sequencing (XR-seq), provides comprehensive profiling of DNA damage repair. A number of XR-seq experiments at a variety of conditions for different damage types revealed heterogenous repair in the human genome. Although human repair profiles were extensively studied, how repair maps vary between primates is yet to be investigated. Here, we characterized the genome-wide UV-induced damage repair in gray mouse lemur,Microcebus murinus, in comparison to human. Mouse lemurs are strictly nocturnal, are the world's smallest living primates, and last shared a common ancestor with humans at least 60 million years ago. We derived fibroblast cell lines from mouse lemur, exposed them to UV irradiation. The following repair events were captured genome-wide through the XR-seq protocol. Mouse lemur repair profiles were analyzed in comparison to the equivalent human fibroblast datasets. We found that overall UV sensitivity, repair efficiency, and transcription-coupled repair levels differ between the two primates. Despite this, comparative analysis of human and mouse lemur fibroblasts revealed that genome-wide repair profiles of the homologous regions are highly correlated. This correlation is stronger for the highly expressed genes. With the inclusion of an additional XR-seq sample derived from another human cell line in the analysis, we found that fibroblasts of the two primates repair UV-induced DNA lesions in a more similar pattern than two distinct human cell lines do. Our results suggest that mouse lemurs and humans, and possibly primates in general, share a homologous repair mechanism as well as genomic variance distribution, albeit with their variable repair efficiency. This result also emphasizes the deep homologies of individual tissue types across the eukaryotic phylogeny.

Go to manuscript