Methods for Studying the DNA Damage Response in the Caenorhabdatis elegans Germ Line

被引:83
作者
Craig, Ashley L. [1 ]
Moser, Sandra C. [1 ]
Bailly, Aymeric P. [1 ,2 ,3 ]
Gartner, Anton [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Wellcome Trust Ctr Gene Regulat & Express, Dundee DD1 4HN, Scotland
[2] Univ Montpellier I, CNRS, CRBM, UMR 5237, F-34006 Montpellier, France
[3] Univ Montpellier 2, CNRS, CRBM, UMR 5237, F-34095 Montpellier 5, France
来源
CAENORHABDITIS ELEGANS: CELL BIOLOGY AND PHYSIOLOGY, SECOND EDITION | 2012年 / 107卷
基金
英国惠康基金;
关键词
PROGRAMMED CELL-DEATH; CHECKPOINT PROTEIN; INDUCED APOPTOSIS; MEIOTIC PROPHASE; CROSSING-OVER; REPAIR; PATHWAY; P53; REPLICATION; STRESS;
D O I
10.1016/B978-0-12-394620-1.00011-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In response to genotoxic insults, cells activate DNA damage response pathways that either stimulate transient cell cycle arrest and DNA repair or induce apoptosis. The Caenorhabditis elegans germ line is now well established as a model system to study these processes in a genetically tractable, multicellular organism. Upon treatment with genotoxic agents, premeiotic C. elegans germ cells transiently halt cell cycle progression, whereas meiotic prophase germ cells in the late-pachytene stage undergo apoptosis. Further, accumulation of unrepaired meiotic recombination intermediates can also lead to apoptosis of affected pachytene cells. DNA damage-induced cell death requires key components of the evolutionarily conserved apoptotic machinery. Moreover, both cell cycle arrest and pachytene apoptosis responses depend on conserved DNA damage checkpoint proteins. Genetics- and genomics-based approaches that have demonstrated roles for conserved checkpoint proteins have also begun to uncover novel components of these response pathways. In this chapter, we briefly review the C. elegans DNA damage response field, discuss in detail methods currently used to assay DNA damage responses in C. elegans, and describe the development of new experimental tools that will facilitate a more comprehensive understanding of the DNA damage response.
引用
收藏
页码:321 / 352
页数:32
相关论文
共 71 条
[1]   Programmed cell death mediated by ced-3 and ced-4 protects Caenorhabditis elegans from Salmonella typhimurium-mediated killing [J].
Aballay, A ;
Ausubel, FM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2735-2739
[2]   MRT-2 checkpoint protein is required for germline immortality and telomere replication in C-elegans [J].
Ahmed, S ;
Hodgkin, J .
NATURE, 2000, 403 (6766) :159-164
[3]   C-elegans RAD-5/CLK-2 defines a new DNA damage checkpoint protein [J].
Ahmed, S ;
Alpi, A ;
Hengartner, MO ;
Gartner, A .
CURRENT BIOLOGY, 2001, 11 (24) :1934-1944
[4]   Genetic and cytological characterization of the recombination protein RAD-51 in Caenorhabditis elegans [J].
Alpi, A ;
Pasierbek, P ;
Gartner, A ;
Loidl, J .
CHROMOSOMA, 2003, 112 (01) :6-16
[5]   The Caenorhabditis elegans Homolog of Gen1/Yen1 Resolvases Links DNA Damage Signaling to DNA Double-Strand Break Repair [J].
Bailly, Aymeric P. ;
Freeman, Alasdair ;
Hall, Julie ;
Declais, Anne-Cecile ;
Alpi, Arno ;
Lilley, David M. J. ;
Ahmed, Shawn ;
Gartner, Anton .
PLOS GENETICS, 2010, 6 (07) :1-16
[6]   PURIFICATION AND CHARACTERIZATION OF THE HUMAN RAD51 PROTEIN, AN ANALOG OF ESCHERICHIA-COLI RECA [J].
BENSON, FE ;
STASIAK, A ;
WEST, SC .
EMBO JOURNAL, 1994, 13 (23) :5764-5771
[7]   Conserved checkpoint monitors meiotic chromosome synapsis in Caenorhabditis elegans [J].
Bhalla, N ;
Dernburg, AF .
SCIENCE, 2005, 310 (5754) :1683-1686
[8]   Combined functional genomic maps of the C-elegans DNA damage response [J].
Boulton, SJ ;
Gartner, A ;
Reboul, J ;
Vaglio, P ;
Dyson, N ;
Hill, DE ;
Vidal, M .
SCIENCE, 2002, 295 (5552) :127-131
[9]   BRCA1/BARD1 orthologs required for DNA repair in Caenorhabditis elegans [J].
Boulton, SJ ;
Martin, JS ;
Polanowska, J ;
Hill, DE ;
Gartner, A ;
Vidal, M .
CURRENT BIOLOGY, 2004, 14 (01) :33-39
[10]  
BRENNER S, 1974, GENETICS, V77, P71