Caenorhabditis elegans DNA mismatch repair gene msh-2 is required for microsatellite stability and maintenance of genome integrity

被引:53
作者
Degtyareva, NP
Greenwell, P
Hofmann, ER
Hengartner, MO
Zhang, L
Culotti, JG
Petes, TD
机构
[1] Univ Zurich, Inst Mol Biol, CH-8057 Zurich, Switzerland
[2] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Curriculum Genet & Mol Biol, Chapel Hill, NC 27599 USA
[4] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[5] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
[6] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
关键词
D O I
10.1073/pnas.032671599
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mismatch repair genes are important in maintaining the fidelity of DNA replication. To determine the function of the Caenorhabditis elegans homologue of the MSH2 mismatch repair gene (msh-2), we isolated a strain of C elegans with an insertion of the transposable element Tc1 within msh-2. Early-passage msh-2 mutants were similar to wild-type worms with regard to lifespan and meiotic chromosome segregation but had slightly reduced fertility. The mutant worms had reduced DNA damage-induced germ-line apoptosis after genotoxic stress. The msh-2 mutants also had elevated levels of microsatellite instability and increased rates of reversion of the dominant unc-58(e665) mutation. In addition, serially passaged cultures of msh-2 worms died out much more quickly than those of wild-type worms. These results demonstrate that msh-2 function in C elegans is important in regulating both short- and long-term genomic stability.
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收藏
页码:2158 / 2163
页数:6
相关论文
共 37 条
  • [1] MRT-2 checkpoint protein is required for germline immortality and telomere replication in C-elegans
    Ahmed, S
    Hodgkin, J
    [J]. NATURE, 2000, 403 (6766) : 159 - 164
  • [2] Genetic and biochemical analysis of Msh2p-Msh6p: Role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition
    Alani, E
    Sokolsky, T
    Studamire, B
    Miret, JJ
    Lahue, RS
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (05) : 2436 - 2447
  • [3] BRENNER S, 1974, GENETICS, V77, P71
  • [4] BUERMEYER AB, 1999, ANNU REV GENET, V33, P359
  • [5] CHEN S, 1999, P NATL ACAD SCI USA, V98, P13802
  • [6] Meiotic recombination in C-elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis
    Dernburg, AF
    McDonald, K
    Moulder, G
    Barstead, R
    Dresser, M
    Villeneuve, AM
    [J]. CELL, 1998, 94 (03) : 387 - 398
  • [7] HIGH-FREQUENCY EXCISION OF TRANSPOSABLE ELEMENT TC1 IN THE NEMATODE CAENORHABDITIS ELEGANS IS LIMITED TO SOMATIC-CELLS
    EMMONS, SW
    YESNER, L
    [J]. CELL, 1984, 36 (03) : 599 - 605
  • [8] Microsatellite instability in Drosophila spellchecker1 (MutS homolog) mutants
    Flores, C
    Engels, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) : 2964 - 2969
  • [9] A conserved checkpoint pathway mediates DNA damage-induced apoptosis and cell cycle arrest in C. elegans
    Gartner, A
    Milstein, S
    Ahmed, S
    Hodgkin, J
    Hengartner, MO
    [J]. MOLECULAR CELL, 2000, 5 (03) : 435 - 443
  • [10] Hadjimarcou MI, 2001, GENETICS, V158, P177