| Literature DB >> 30636294 |
Kostlend Mara1, Florence Charlot1, Anouchka Guyon-Debast1, Didier G Schaefer2, Cécile Collonnier1, Mathilde Grelon1, Fabien Nogué1.
Abstract
Double-stranded breaks can be repaired by different mechanisms such as homologous recombination (HR), classical nonhomologous end joining (C-NHEJ) and alternative end joining (Alt-EJ). Polymerase Q (POLQ) has been proposed to be the main factor involved in Alt-EJ-mediated DNA repair. Here we describe the role of POLQ in DNA repair and gene targeting in Physcomitrella patens. The disruption of the POLQ gene does not influence the genetic stability of P. patens nor its development. The polq mutant shows the same sensitivity as wild-type towards most of the genotoxic agents tested (ultraviolet (UV), methyl methanesulfonate (MMS) and cisplatin) with the notable exception of bleomycin for which it shows less sensitivity than the wild-type. Furthermore, we show that POLQ is involved in the repair of CRISPR-Cas9-induced double-stranded breaks in P. patens. We also demonstrate that POLQ is a potential competitor and/or inhibitor of the HR repair pathway. This finding has a consequence in terms of genetic engineering, as in the absence of POLQ the frequency of gene targeting is significantly increased and the number of clean two-sided HR-mediated insertions is enhanced. Therefore, the control of POLQ activity in plants could be a useful strategy to optimize the tools of genome engineering for plant breeding.Entities:
Keywords: zzm321990Physcomitrella patenszzm321990; CRISPR-Cas9; alternative end joining (Alt-EJ); gene targeting; polymerase Q (POLQ)
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Year: 2019 PMID: 30636294 DOI: 10.1111/nph.15680
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151