Drosophila DNA polymerase theta utilizes both helicase-like and polymerase domains during microhomology-mediated end joining and interstrand crosslink repair-Reference-Cited by-同舟云学术

Drosophila DNA polymerase theta utilizes both helicase-like and polymerase domains during microhomology-mediated end joining and interstrand crosslink repair

Published:2017-05-25 Issue:5 Volume:13 Page:e1006813
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Beagan Kelly,Armstrong Robin L.,Witsell Alice,Roy Upasana^ORCID,Renedo Nikolai,Baker Amy E.,Schärer Orlando D.,McVey Mitch^ORCID

Funder

Directorate for Biological Sciences

National Institute of General Medical Sciences

National Institutes of Health

Korean Institute for Basic Science

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference61 articles.

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3. Crosstalk between translesion synthesis, Fanconi anemia network, and homologous recombination repair pathways in interstrand DNA crosslink repair and development of chemoresistance;B Haynes;Mutat Res Rev Mutat Res,2015

4. DNA damage response factors from diverse pathways, including DNA crosslink repair, mediate alternative end joining;SM Howard;PLoS Genet,2015

5. mus308 mutants of Drosophila exhibit hypersensitivity to DNA cross-linking agents and are defective in a deoxyribonuclease;JB Boyd;Genetics,1990

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