Literature DB >> 14643433

Role of the error-free damage bypass postreplication repair pathway in the maintenance of genomic stability.

Marina Smirnova1, Hannah L Klein.   

Abstract

The postreplication repair pathway (PRR) is composed of error-free and error-prone sub-pathways that allow bypass of DNA damage-induced replication-blocking lesions. The error-free sub-pathway is also used for bypass of spontaneous DNA damage and functions in cooperation with recombination pathways. In diploid yeast cells, error-free PRR is needed to prevent genomic instability, which is manifest as loss of heterozygosity (LOH) events of increased chromosome loss and recombination. Homologous recombination acts synergistically with the error-free damage avoidance branch of PRR to prevent chromosome loss. The DNA damage checkpoint gene MEC1 acts synergistically with the PRR pathway in maintaining genomic stability. Integration of the PRR pathway with other cellular pathways for preventing genomic instability is discussed. In diploid strains, the most dramatic increase is in the abnormality of chromosome loss when a repair or damage detection pathway is defective.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14643433     DOI: 10.1016/j.mrfmmm.2003.08.026

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  24 in total

1.  Ubiquitinated proliferating cell nuclear antigen activates translesion DNA polymerases eta and REV1.

Authors:  Parie Garg; Peter M Burgers
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-12       Impact factor: 11.205

2.  Postreplication repair inhibits CAG.CTG repeat expansions in Saccharomyces cerevisiae.

Authors:  Danielle L Daee; Tony Mertz; Robert S Lahue
Journal:  Mol Cell Biol       Date:  2006-10-23       Impact factor: 4.272

3.  Roles of RAD6 epistasis group members in spontaneous polzeta-dependent translesion synthesis in Saccharomyces cerevisiae.

Authors:  Brenda K Minesinger; Sue Jinks-Robertson
Journal:  Genetics       Date:  2005-01-31       Impact factor: 4.562

4.  HARPing on about the DNA damage response during replication.

Authors:  Robert Driscoll; Karlene A Cimprich
Journal:  Genes Dev       Date:  2009-10-15       Impact factor: 11.361

5.  The human F-Box DNA helicase FBH1 faces Saccharomyces cerevisiae Srs2 and postreplication repair pathway roles.

Authors:  Irene Chiolo; Marco Saponaro; Anastasia Baryshnikova; Jeong-Hoon Kim; Yeon-Soo Seo; Giordano Liberi
Journal:  Mol Cell Biol       Date:  2007-08-27       Impact factor: 4.272

6.  Mrc1 is required for sister chromatid cohesion to aid in recombination repair of spontaneous damage.

Authors:  Hong Xu; Charles Boone; Hannah L Klein
Journal:  Mol Cell Biol       Date:  2004-08       Impact factor: 4.272

Review 7.  Suppression of gross chromosomal rearrangements by a new alternative replication factor C complex.

Authors:  Soma Banerjee; Nilabja Sikdar; Kyungjae Myung
Journal:  Biochem Biophys Res Commun       Date:  2007-07-31       Impact factor: 3.575

8.  Polyubiquitination of proliferating cell nuclear antigen by HLTF and SHPRH prevents genomic instability from stalled replication forks.

Authors:  Akira Motegi; Hung-Jiun Liaw; Kyoo-Young Lee; Henk P Roest; Alex Maas; Xiaoli Wu; Helen Moinova; Sanford D Markowitz; Hao Ding; Jan H J Hoeijmakers; Kyungjae Myung
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-21       Impact factor: 11.205

Review 9.  Srs2: the "Odd-Job Man" in DNA repair.

Authors:  Victoria Marini; Lumir Krejci
Journal:  DNA Repair (Amst)       Date:  2010-01-21

10.  Functional significance of the Rad51-Srs2 complex in Rad51 presynaptic filament disruption.

Authors:  Sierra Colavito; Margaret Macris-Kiss; Changhyun Seong; Olive Gleeson; Eric C Greene; Hannah L Klein; Lumir Krejci; Patrick Sung
Journal:  Nucleic Acids Res       Date:  2009-09-10       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.