Timely anaphase onset requires a novel spindle and kinetochore complex comprising Ska1 and Ska2

被引:208
作者
Hanisch, Anja [1 ]
Sillje, Herman H. W. [1 ]
Nigg, Erich A. [1 ]
机构
[1] Max Planck Inst Biochem, Dept Cell Biol, D-82152 Martinsried, Germany
关键词
kinetochore; Mad2; metaphase; microtubules; spindle checkpoint;
D O I
10.1038/sj.emboj.7601426
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
Chromosome segregation during mitosis requires chromosomes to undergo bipolar attachment on spindle microtubules (MTs) and subsequent silencing of the spindle checkpoint. Here, we describe the identification and characterisation of a novel spindle and kinetochore (KT)associated complex that is required for timely anaphase onset. The complex comprises at least two proteins, termed Ska1 ((S) under bar pindle and (K) under barT (A) under bar ssociated 1) and Ska2. Ska1 associates with KTs following MT attachment during prometaphase. Ska1 and Ska2 interact with each other and Ska1 is required for Ska2 stability in vivo. Depletion of either Ska1 or Ska2 by small interfering RNA results in the loss of both proteins from the KT. The absence of Ska proteins does not disrupt overall KT structure, but KT fibres show an increased cold-sensitivity. Most strikingly, Ska-depleted cells undergo a prolonged checkpoint-dependent delay in a metaphase-like state. This delay is characterised by the recruitment of Mad2 protein to a few KTs and the occasional loss of individual chromosomes from the metaphase plate. These data suggest that the Ska1/2 complex plays a critical role in the maintenance of the metaphase plate and/or spindle checkpoint silencing.
引用
收藏
页码:5504 / 5515
页数:12
相关论文
共 35 条
[1]   Captivating capture: How microtubules attach to kinetochores [J].
Biggins, S ;
Walczak, CE .
CURRENT BIOLOGY, 2003, 13 (11) :R449-R460
[2]   Implication of a novel multiprotein Dam1p complex in outer kinetochore function [J].
Cheeseman, IM ;
Brew, C ;
Wolyniak, M ;
Desai, A ;
Anderson, S ;
Muster, N ;
Yates, JR ;
Huffaker, TC ;
Drubin, DG ;
Barnes, G .
JOURNAL OF CELL BIOLOGY, 2001, 155 (07) :1137-1145
[3]   Architecture of the human Ndc80-Hec1 complex, a critical constituent of the outer kinetochore [J].
Ciferri, C ;
De Luca, J ;
Monzani, S ;
Ferrari, KJ ;
Ristic, D ;
Wyman, C ;
Stark, H ;
Kilmartin, J ;
Salmon, ED ;
Musacchio, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (32) :29088-29095
[4]   Centromeres and kinetochores: From epigenetics to mitotic checkpoint signaling [J].
Cleveland, DW ;
Mao, YH ;
Sullivan, KF .
CELL, 2003, 112 (04) :407-421
[5]   hNuf2 inhibition blocks stable kinetochore-microtubule attachment and induces mitotic cell death in HeLa cells [J].
DeLuca, JG ;
Moree, B ;
Hickey, JM ;
Kilmartin, JV ;
Salmon, ED .
JOURNAL OF CELL BIOLOGY, 2002, 159 (04) :549-555
[6]   Hec1 and Nuf2 are core components of the kinetochore outer plate essential for organizing microtubule attachment sites [J].
DeLuca, JG ;
Dong, YM ;
Hergert, P ;
Strauss, J ;
Hickey, JM ;
Salmon, ED ;
McEwen, BF .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (02) :519-531
[7]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[8]   Measuring the stoichiometry and physical interactions between components elucidates the architecture of the vertebrate kinetochore [J].
Emanuele, MJ ;
McCleland, ML ;
Satinover, DL ;
Stukenberg, PT .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (10) :4882-4892
[9]   Different Plk1 functions show distinct dependencies on polo-box domain-mediated targeting [J].
Hanisch, A ;
Wehner, A ;
Nigg, EA ;
Silljé, HHW .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (01) :448-459
[10]   Saccharomyces cerevisiae Duo1p and Dam1p, novel proteins involved in mitotic spindle function [J].
Hofmann, C ;
Cheeseman, IM ;
Goode, BL ;
McDonald, KL ;
Barnes, G ;
Drubin, DG .
JOURNAL OF CELL BIOLOGY, 1998, 143 (04) :1029-1040