The INO80 complex is required for damage-induced recombination

被引:30
作者
Kawashima, Satoshi
Ogiwara, Hideaki
Tada, Shusuke
Harata, Masahiko
Wintersberger, Ulrike
Enomoto, Takemi
Seki, Masayuki
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Mol Cell Biol Lab, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Tohoku Univ, Grad Sch Agr Sci, Div Life Sci,Lab Mol Biol, Dept Mol & Cell Biol, Sendai, Miyagi 9818555, Japan
[3] Univ Vienna, Inst Canc Res, Div Mol Genet, A-1090 Vienna, Austria
[4] Tohoku Univ, 21st Century COE Program, Comprehens Res & Educ Ctr Planning Drug Dev & Cli, Sendai, Miyagi 9808578, Japan
关键词
INO80; SWR1; NuA4; Arp4; Arp5; Arp6; Arp8; recombination; repair; chromatin remodeling;
D O I
10.1016/j.bbrc.2007.02.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The budding yeast INO80 complex has a role in remodeling chromatin structure, and the SWR1 complex replaces a H2A/H2B dimer with a variant dimer, H2A.Z (Htz1)/H2B. It has been reported that these chromatin remodeling complexes contain Arp4 (actin-related protein) and actin in common and are recruited to HO endonuclease-induced DNA double-strand break (DSB) site. Reportedly, Ino80 can evict nucleosomes surrounding a HO-induced DSB; however, it has no apparent role to play in the repair of HO-induced DSB. Here we show that an essential factor for INO80 chromatin remodeling activity, Arp8, is involved in damage-induced sister chromatid recombination and interchromosomal recombination between heteroallales. In contrast, arp6 mutants are proficient for recombination, indicating that the SWRI complex does not promote recombination. Our data suggest that the remodeling of chromatin by the INO80 complex facilitates efficient homologus recombination upon DNA damages. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:835 / 841
页数:7
相关论文
共 30 条
  • [1] DSB repair: the yeast paradigm
    Aylon, Y
    Kupiec, M
    [J]. DNA REPAIR, 2004, 3 (8-9) : 797 - 815
  • [2] Acetylation of histone H4 by Esa1 is required for DNA double-strand break repair
    Bird, AW
    Yu, DY
    Pray-Grant, MG
    Qiu, QF
    Harmon, KE
    Megee, PC
    Grant, PA
    Smith, MM
    Christman, MF
    [J]. NATURE, 2002, 419 (6905) : 411 - 415
  • [3] Bressan DA, 1999, MOL CELL BIOL, V19, P7681
  • [4] Binding of chromatin-modifying activities to phosphorylated histone H2A at DNA damage sites
    Downs, JA
    Allard, S
    Jobin-Robitaille, O
    Javaheri, A
    Auger, A
    Bouchard, N
    Kron, SJ
    Jackson, SP
    Côté, J
    [J]. MOLECULAR CELL, 2004, 16 (06) : 979 - 990
  • [5] The actin-related proteins
    Frankel, S
    Mooseker, MS
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (01) : 30 - 37
  • [6] The INO80 protein controls homologous recombination in Arabidopsis thaliana
    Fritsch, O
    Benvenuto, G
    Bowler, C
    Molinier, J
    Hohn, B
    [J]. MOLECULAR CELL, 2004, 16 (03) : 479 - 485
  • [7] The nuclear actin-related protein Act3p/Arp4p of Saccharomyces cerevisiae is involved in transcription regulation of stress genes
    Görzer, I
    Schüller, C
    Heidenreich, E
    Krupanska, L
    Kuchler, K
    Wintersberger, U
    [J]. MOLECULAR MICROBIOLOGY, 2003, 50 (04) : 1155 - 1171
  • [8] Uses and abuses of HO endonuclease
    Haber, JE
    [J]. GUIDE TO YEAST GENETICS AND MOLECULAR AND CELL BIOLOGY, PT B, 2002, 350 : 141 - 164
  • [9] The nuclear actin-related protein of Saccharomyces cerevisiae, Act3p/Arp4, interacts with core histones
    Harata, M
    Oma, Y
    Mizuno, S
    Jiang, YW
    Stillman, DJ
    Wintersberger, U
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (08) : 2595 - 2605
  • [10] MUTATIONS IN XRS2 AND RAD50 DELAY BUT DO NOT PREVENT MATING-TYPE SWITCHING IN SACCHAROMYCES-CEREVISIAE
    IVANOV, EL
    SUGAWARA, N
    WHITE, CI
    FABRE, F
    HABER, JE
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) : 3414 - 3425