Regulation of sister chromatid cohesion between chromosome arms

被引:209
作者
Giménez-Abián, JF
Sumara, I
Hirota, T
Hauf, S
Gerlich, D
de la Torre, C
Ellenberg, J
Peters, JM
机构
[1] Res Inst Mol Pathol, A-1030 Vienna, Austria
[2] CSIC, Ctr Invest Biol, Madrid 28040, Spain
[3] European Mol Biol Lab, D-69117 Heidelberg, Germany
基金
日本学术振兴会;
关键词
D O I
10.1016/j.cub.2004.06.052
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Sister chromatid separation in anaphase depends on the removal of cohesin complexes from chromosomes [1]. In vertebrates, the bulk of cohesin is already removed from chromosome arms during prophase and prometaphase [2,3], whereas cohesin remains at centromeres until metaphase, when cohesin is cleaved by the protease separase [3, 4]. In unperturbed mitoses, arm cohesion nevertheless persists throughout metaphase and is principally sufficient to maintain sister chromatid cohesion [5]. How arm cohesion is maintained until metaphase is unknown. Here we show that small amounts of cohesin can be detected in the interchromatid region of metaphase chromosome arms. If prometaphase is prolonged by treatment of cells with microtubule poisons, these cohesin complexes dissociate from chromosome arms, and arm cohesion is dissolved. If cohesin dissociation in prometaphase-arrested cells is prevented by depletion of Plk1 or inhibition of Aurora B, arm cohesion is maintained. These observations imply that, in unperturbed mitoses, small amounts of cohesin maintain arm cohesion until metaphase. When cells lacking Plk1 and Aurora B activity enter anaphase, chromatids lose cohesin. This loss is prevented by proteasome inhibitors, implying that it depends on separase activation. Separase may therefore be able to cleave cohesin at centromeres and on chromosome arms.
引用
收藏
页码:1187 / 1193
页数:7
相关论文
共 20 条
[1]
A potential role for human cohesin in mitotic spindle aster assembly [J].
Gregson, HC ;
Schmiesing, JA ;
Kim, JS ;
Kobayashi, T ;
Zhou, S ;
Yokomori, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (50) :47575-47582
[2]
Building and breaking bridges between sister chromatids [J].
Haering, CH ;
Nasmyth, K .
BIOESSAYS, 2003, 25 (12) :1178-1191
[3]
The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint [J].
Hauf, S ;
Cole, RW ;
LaTerra, S ;
Zimmer, C ;
Schnapp, G ;
Walter, R ;
Heckel, A ;
van Meel, J ;
Rieder, CL ;
Peters, JM .
JOURNAL OF CELL BIOLOGY, 2003, 161 (02) :281-294
[4]
Cohesin cleavage by separase required for anaphase and cytokinesis in human cells [J].
Hauf, S ;
Waizenegger, IC ;
Peters, JM .
SCIENCE, 2001, 293 (5533) :1320-1323
[5]
Human chromatid cohesin component hRad21 is phosphorylated in M phase and associated with metaphase centromeres [J].
Hoque, MT ;
Ishikawa, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) :5059-5067
[6]
Levan A, 1938, HEREDITAS, V24, P471
[7]
Cohesin release is required for sister chromatid resolution, but not for condensin-mediated compaction, at the onset of mitosis [J].
Losada, A ;
Hirano, M ;
Hirano, T .
GENES & DEVELOPMENT, 2002, 16 (23) :3004-3016
[8]
Identification of Xenopus SMC protein complexes required for sister chromatid cohesion [J].
Losada, A ;
Hirano, M ;
Hirano, T .
GENES & DEVELOPMENT, 1998, 12 (13) :1986-1997
[9]
Identification and characterization of SA/Scc3p subunits in the Xenopus and human cohesin complexes [J].
Losada, A ;
Yokochi, T ;
Kobayashi, R ;
Hirano, T .
JOURNAL OF CELL BIOLOGY, 2000, 150 (03) :405-416
[10]
Ludford RJ, 1936, ARCH EXP ZELLFORSCH, V18, P411