A Central Coupler for Recombination Initiation Linking Chromosome Architecture to S Phase Checkpoint

被引:75
作者
Miyoshi, Tomoichiro [1 ]
Ito, Masaru [1 ]
Kugou, Kazuto [1 ]
Yamada, Shintaro [1 ,2 ]
Furuichi, Masaki [3 ]
Oda, Arisa [1 ,2 ]
Yamada, Takatomi [1 ]
Hirota, Kouji [1 ]
Masai, Hisao [3 ]
Ohta, Kunihiro [1 ,2 ]
机构
[1] Univ Tokyo, Dept Life Sci, Meguro Ku, Tokyo 1538902, Japan
[2] Univ Tokyo, Dept Biochem & Biophys, Bunkyo Ku, Tokyo 1138654, Japan
[3] Tokyo Metropolitan Inst Med Sci, Genome Dynam Project, Setagaya Ku, Tokyo 1568506, Japan
关键词
MEIOTIC DNA BREAKAGE; SISTER-CHROMATID COHESION; LINEAR ELEMENTS; PROTEINS; MEIOSIS; GENE; COMPLEX; REPLICATION; EXPRESSION; PRDM9;
D O I
10.1016/j.molcel.2012.06.023
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
Higher-order chromosome structure is assumed to control various DNA-templated reactions in eukaryotes. Meiotic chromosomes implement developed structures called "axes" and "loops"; both are suggested to tether each other, activating Spoil to catalyze meiotic DNA double-strand breaks (DSBs) at recombination hotspots. We found that the Schizosaccharomyces pombe Spo11 homolog Red 12 and its partners form two distinct subcomplexes, DSBC (Rec6-Rec12-Rec14) and SFT (Rec7-Rec15-Rec24). Mde2, whose expression is strictly regulated by the replication checkpoint, interacts with Rec15 to stabilize the SFT subcomplex and further binds Rec14 in DSBC. Rec10 provides a docking platform for SFT binding to axes and can partially interact with DSB sites located in loops depending upon Mde2, which is indicative of the formation of multiprotein-based tethered axis-loop complex. These data lead us to propose a mechanism by which Mde2 functions as a recombination initiation mediator to tether axes and loops, in liaison with the meiotic replication checkpoint.
引用
收藏
页码:722 / 733
页数:12
相关论文
共 54 条
[1]  
Abe H, 2000, GENETICS, V154, P1497
[2]   Antiviral protein Ski8 is a direct partner of Spo11 in meiotic DNA break formation, independent of its cytoplasmic role in RNA metabolism [J].
Arora, C ;
Kee, K ;
Maleki, S ;
Keeney, S .
MOLECULAR CELL, 2004, 13 (04) :549-559
[3]   PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice [J].
Baudat, F. ;
Buard, J. ;
Grey, C. ;
Fledel-Alon, A. ;
Ober, C. ;
Przeworski, M. ;
Coop, G. ;
de Massy, B. .
SCIENCE, 2010, 327 (5967) :836-840
[4]   A positive but complex association between meiotic double-strand break hotspots and open chromatin in Saccharomyces cerevisiae [J].
Berchowitz, Luke E. ;
Hanlon, Sean E. ;
Lieb, Jason D. ;
Copenhaver, Gregory P. .
GENOME RESEARCH, 2009, 19 (12) :2245-2257
[5]   An atypical topoisomerase II from archaea with implications for meiotic recombination [J].
Bergerat, A ;
deMassy, B ;
Gadelle, D ;
Varoutas, PC ;
Nicolas, A ;
Forterre, P .
NATURE, 1997, 386 (6623) :414-417
[6]   Physical and functional interactions among basic chromosome organizational features govern early steps of meiotic chiasma formation [J].
Blat, Y ;
Protacio, RU ;
Hunter, N ;
Kleckner, N .
CELL, 2002, 111 (06) :791-802
[7]   Direct coupling between meiotic DNA replication and recombination initiation [J].
Borde, V ;
Goldman, ASH ;
Lichten, M .
SCIENCE, 2000, 290 (5492) :806-809
[8]   Meiotic DNA breaks associated with recombination in S. pombe [J].
Cervantes, MD ;
Farah, JA ;
Smith, GR .
MOLECULAR CELL, 2000, 5 (05) :883-888
[9]   Rec25 and Rec27, novel linear-element components, link cohesin to meiotic DNA breakage and recombination [J].
Davis, Luther ;
Rozalen, Ana E. ;
Moreno, Sergio ;
Smith, Gerald R. ;
Martin-Castellanos, Cristina .
CURRENT BIOLOGY, 2008, 18 (11) :849-854
[10]  
DEVEAUX LC, 1992, GENETICS, V130, P251