Rec8 phosphorylation and recombination promote the step-wise loss of cohesins in meiosis

被引:106
作者
Brar, Gloria A. [1 ]
Kiburz, Brendan M. [1 ]
Zhang, Yi [1 ]
Kim, Ji-Eun [1 ]
White, Forest [1 ]
Amon, Angelika [1 ]
机构
[1] MIT, Howard Hughes Med Inst, Ctr Canc Res, Cambridge, MA 02139 USA
关键词
D O I
10.1038/nature04794
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
During meiosis, cohesins-protein complexes that hold sister chromatids together-are lost from chromosomes in a step-wise manner(1). Loss of cohesins from chromosome arms is necessary for homologous chromosomes to segregate during meiosis I. Retention of cohesins around centromeres until meiosis II is required for the accurate segregation of sister chromatids. Here we show that phosphorylation of the cohesin subunit Rec8 contributes to step-wise cohesin removal. Our data further implicate two other key regulators of meiotic chromosome segregation, the cohesin protector Sgo1 and meiotic recombination in bringing about the step-wise loss of cohesins and thus the establishment of the meiotic chromosome segregation pattern. Understanding the interplay between these processes should provide insight into the events underlying meiotic chromosome mis-segregation, the leading cause of miscarriages and mental retardation in humans.
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页码:532 / 536
页数:5
相关论文
共 28 条
[1]   ANALYSIS OF WILD-TYPE AND RAD50 MUTANTS OF YEAST SUGGESTS AN INTIMATE-RELATIONSHIP BETWEEN MEIOTIC CHROMOSOME SYNAPSIS AND RECOMBINATION [J].
ALANI, E ;
PADMORE, R ;
KLECKNER, N .
CELL, 1990, 61 (03) :419-436
[2]   Phosphorylation of the cohesin subunit Scc1 by Polo/Cdc5 kinase regulates sister chromatid separation in yeast [J].
Alexandru, G ;
Uhlmann, F ;
Mechtler, K ;
Poupart, MA ;
Nasmyth, K .
CELL, 2001, 105 (04) :459-472
[3]   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
[4]   DMC1 - A MEIOSIS-SPECIFIC YEAST HOMOLOG OF ESCHERICHIA-COLI RECA REQUIRED FOR RECOMBINATION, SYNAPTONEMAL COMPLEX-FORMATION, AND CELL-CYCLE PROGRESSION [J].
BISHOP, DK ;
PARK, D ;
XU, LZ ;
KLECKNER, N .
CELL, 1992, 69 (03) :439-456
[5]   Disjunction of homologous chromosomes in meiosis I depends on proteolytic cleavage of the meiotic cohesin Rec8 by separin [J].
Buonomo, SBC ;
Clyne, RK ;
Fuchs, J ;
Loidl, J ;
Uhlmann, F ;
Nasmyth, K .
CELL, 2000, 103 (03) :387-398
[6]   Division of the nucleolus and its release of CDC14 during anaphase of meiosis I depends on separase, SPO12, and SLK19 [J].
Buonomo, SBC ;
Rabitsch, KP ;
Fuchs, J ;
Gruber, S ;
Sullivan, M ;
Uhlmann, F ;
Petronczki, M ;
Tóth, A ;
Nasmyth, K .
DEVELOPMENTAL CELL, 2003, 4 (05) :727-739
[7]   Polo-like kinase Cdc5 promotes chiasmata formation and cosegregation of sister centromeres at meiosis I [J].
Clyne, RK ;
Katis, VL ;
Jessop, L ;
Benjamin, KR ;
Herskowitz, I ;
Lichten, M ;
Nasmyth, K .
NATURE CELL BIOLOGY, 2003, 5 (05) :480-485
[8]   Anaphase initiation in Saccharomyces cerevisiae is controlled by the APC-dependent degradation of the anaphase inhibitor Pds1p [J].
CohenFix, O ;
Peters, JM ;
Kirschner, MW ;
Koshland, D .
GENES & DEVELOPMENT, 1996, 10 (24) :3081-3093
[9]   Preferential cleavage of chromatin-bound cohesin after targeted phosphorylation by Polo-like kinase [J].
Hornig, NCD ;
Uhlmann, F .
EMBO JOURNAL, 2004, 23 (15) :3144-3153
[10]   Maintenance of cohesin at centromeres after meiosis I in budding yeast requires a kinetochore-associated protein related to MEI-S332 [J].
Katis, VL ;
Galova, M ;
Rabitsch, KP ;
Gregan, J ;
Nasmyth, K .
CURRENT BIOLOGY, 2004, 14 (07) :560-572