Fission yeast Mes1p ensures the onset of meiosis II by blocking degradation of cyclin Cdc13p

被引:64
作者
Izawa, D
Goto, M
Yamashita, A
Yamano, H
Yamamoto, M [1 ]
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Biophys & Biochem, Tokyo 1130033, Japan
[2] Univ Tokyo, Mol Genet Res Lab, Tokyo 1130033, Japan
[3] Natl Inst Basic Biol, Dept Cell Proliferat, Okazaki, Aichi 4440867, Japan
[4] Marie Curie Res Inst, Cell Cycle Control Grp, Surrey RH8 0TL, England
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature03406
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
Meiosis is a special form of nuclear division to generate eggs, spermand spores in eukaryotes. Meiosis consists of the first (MI) and the second (MII) meiotic divisions, which occur consecutively. MI is reductional, in which homologous chromosomes derived from parents segregate. MI is supported by an elaborate mechanism involving meiosis-specific cohesin and its protector(1). MII is equational, in which replicated sister-chromatids separate as in mitosis. MII is generally considered to mimic mitosis in mechanism. However, fission yeastMes1p is essential for MII but dispensable for mitosis. The mes1-B44 mutant arrests before MII2. Transcription of mes1 is low in vegetative cells and boosted in a narrow window between late MI and late MII3. The mes1 mRNA undergoes meiosis-specific splicing(4). Here we show that Mes1p is a factor that suppresses the degradation of cyclin Cdc13p at anaphase I. Mes1p binds to Slp1p, an activator of APC/C ( anaphase promoting complex/cyclosome), and counteracts its function to engage Cdc13p in proteolysis. Inhibition of APC/C-dependent degradation of Cdc13p by Mes1p was reproduced in a Xenopus egg extract. We therefore propose that Mes1p has a key function in saving a sufficient level of MPF ( M-phase-promoting factor) activity required for the execution of MII.
引用
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页码:529 / 533
页数:5
相关论文
共 30 条
[1]  
Blanco MA, 2001, J CELL SCI, V114, P2135
[2]   The G1/S cyclin Cig2p during meiosis in fission yeast [J].
Borgne, A ;
Murakami, H ;
Ayté, J ;
Nurse, P .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (06) :2080-2090
[3]   2 FISSION YEAST B-TYPE CYCLINS, CIG2 AND CDC13, HAVE DIFFERENT FUNCTIONS IN MITOSIS [J].
BUENO, A ;
RUSSELL, P .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2286-2297
[4]   D box and KEN box motifs in budding yeast Hsl1p are required for APC-mediated degradation and direct binding to Cdc20p and Cdh1p [J].
Burton, JL ;
Solomon, MJ .
GENES & DEVELOPMENT, 2001, 15 (18) :2381-2395
[5]  
Decottignies A, 2001, J CELL SCI, V114, P2627
[6]   Direct binding of CDC20 protein family members activates the anaphase-promoting complex in mitosis and G1 [J].
Fang, GW ;
Yu, HT ;
Kirschner, MW .
MOLECULAR CELL, 1998, 2 (02) :163-171
[7]   Cut2 proteolysis required for sister-chromatid separation in fission yeast [J].
Funabiki, H ;
Yamano, H ;
Kumada, K ;
Nagao, K ;
Hunt, T ;
Yanagida, M .
NATURE, 1996, 381 (6581) :438-441
[8]   TYROSINE PHOSPHORYLATION OF THE FISSION YEAST CDC2+ PROTEIN-KINASE REGULATES ENTRY INTO MITOSIS [J].
GOULD, KL ;
NURSE, P .
NATURE, 1989, 342 (6245) :39-45
[9]   The Schizosaccharomyces pombe spindle checkpoint protein mad2p blocks anaphase and genetically interacts with the anaphase-promoting complex [J].
He, XW ;
Patterson, TE ;
Sazer, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :7965-7970
[10]   Residual Cdc2 activity remaining at meiosis I exit is essential for meiotic M-M transition in Xenopus oocyte extracts [J].
Iwabuchi, M ;
Ohsumi, K ;
Yamamoto, TM ;
Sawada, W ;
Kishimoto, T .
EMBO JOURNAL, 2000, 19 (17) :4513-4523