Mammalian polymerase ζ is essential for post-replication repair of UV-induced DNA lesions

被引:58
作者
Jansen, Jacob G. [1 ]
Tsaalbi-Shtylik, Anastasia [1 ]
Hendriks, Giel [1 ]
Verspuy, Johan [1 ]
Gali, Himabindu [2 ]
Haracska, Lajos [2 ]
de Wind, Niels [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Toxicogenet, NL-2300 RC Leiden, Netherlands
[2] Hungarian Acad Sci, Biol Res Ctr, Inst Genet, H-6726 Szeged, Hungary
关键词
DNA translesion synthesis; Post-replication repair; DNA damage bypass; Rev3; Ultraviolet light; Mammalian cells; CELL NUCLEAR ANTIGEN; SACCHAROMYCES-CEREVISIAE; TRANSLESION SYNTHESIS; REV1; PROTEIN; EMBRYONIC LETHALITY; CATALYTIC SUBUNIT; POL-ZETA; GENOMIC INSTABILITY; INDUCED MUTATIONS; UBIQUITIN LIGASE;
D O I
10.1016/j.dnarep.2009.09.006
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
DNA polymerase zeta is believed to be an essential constituent of DNA damage tolerance, comprising several pathways that allow the replication of DNA templates containing unrepaired damage. We wanted to better define the role of polymerase zeta in DNA damage tolerance in mammalian cells. To this aim we have investigated replication of ultraviolet light-damaged DNA templates in mouse embryonic fibroblasts deficient for Rev3, the catalytic subunit of polymerase zeta. We found that Rev3 is important for a post-replication repair pathway of helix-distorting [6-4]pyrimidine-pyrimidone photoproducts and, to a lesser extent, of cyclobutaine pyrimidine dimers. Unlike its partner Rev1, Rev3 appears not to be involved in an immediate translesion synthesis pathway at a stalled replication fork. The deficiency of Rev3(-/-) MEFs in post-replication repair of different photoproducts contributes to the extreme sensitivity of these cells to UV light. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1444 / 1451
页数:8
相关论文
共 56 条
[1]
Complex formation with Rev1 enhances the proficiency of Saccharomyces cerevisiae DNA polymerase for mismatch extension and for extension opposite from DNA lesions [J].
Acharya, Narottam ;
Johnson, Robert E. ;
Prakash, Satya ;
Prakash, Louise .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (24) :9555-9563
[2]
[Anonymous], 2005, DNA Repair and Mutagenesis
[3]
Distinct roles for Rev1p and Rev7p during translesion synthesis in Saccharomyces cerevisiae [J].
Baynton, K ;
Bresson-Roy, A ;
Fuchs, RPP .
MOLECULAR MICROBIOLOGY, 1999, 34 (01) :124-133
[4]
Disruption of mouse polymerase ζ (Rev3) leads to embryonic lethality and impairs blastocyst development in vitro [J].
Bemark, M ;
Khamlichi, AA ;
Davies, SL ;
Neuberger, MS .
CURRENT BIOLOGY, 2000, 10 (19) :1213-1216
[5]
Yeast Rad5 protein required for postreplication repair has a DNA helicase activity specific for replication fork regression [J].
Blastyák, Andras ;
Pintér, Lajos ;
Unk, Ildiko ;
Prakash, Louise ;
Prakash, Satya ;
Haracska, Lajos .
MOLECULAR CELL, 2007, 28 (01) :167-175
[6]
hMMS2 serves a redundant role in human PCNA polyubiquitination [J].
Brun, Jan ;
Chiu, Roland ;
Lockhart, Katherine ;
Xiao, Wei ;
Wouters, Bradly G. ;
Gray, Douglas A. .
BMC MOLECULAR BIOLOGY, 2008, 9
[7]
Monoubiquitination of proliferating cell nuclear antigen induced by stalled replication requires uncoupling of DNA polymerase and mini-chromosome maintenance helicase activities [J].
Chang, Debbie J. ;
Lupardus, Patrick J. ;
Cimprich, Karlene A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (43) :32081-32088
[8]
Lysine 63-polyubiquitination guards against translesion synthesis-induced mutations [J].
Chiu, Roland K. ;
Brun, Jan ;
Ramaekers, Chantal ;
Theys, Jan ;
Weng, Lin ;
Lambin, Philippe ;
Gray, Douglas A. ;
Wouters, Bradly G. .
PLOS GENETICS, 2006, 2 (07) :1070-1083
[9]
Diaz M, 2003, MOL CANCER RES, V1, P836
[10]
Disruption of the Rev3l-encoded catalytic subunit of polymerase ζ in mice results in early embryonic lethality [J].
Esposito, G ;
Godin, I ;
Klein, U ;
Yaspo, ML ;
Cumano, A ;
Rajewsky, K .
CURRENT BIOLOGY, 2000, 10 (19) :1221-1224