Proteomics analysis identifies new components of the fission and budding yeast anaphase-promoting complexes

被引:86
作者
Yoon, HJ
Feoktistova, A
Wolfe, BA
Jennings, JL
Link, AJ
Gould, KL
机构
[1] Vanderbilt Univ, Sch Med, Howard Hughes Med Inst, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Microbiol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Sch Med, Dept Immunol, Nashville, TN 37232 USA
关键词
D O I
10.1016/S0960-9822(02)01331-3
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
The anaphase-promoting complex (APC) is a conserved multisubunit ubiquitin ligase required for the degradation of key cell cycle regulators. Components of the APC have been identified through genetic screens in both Schizosaccharomyces pombe and Saccharomyces cerevisiae as well as through, biochemical purification coupled with mass spectrometric protein identification. With these approaches, 11 subunits of the core S. cerevisiae APC have been identified. Here, we have applied a tandem affinity purification approach coupled with direct analysis of the purified complexes by mass spectrometry (DALPC) to reveal additional subunits of both the S. pombe and S. cerevisiae APCs. Our data increase the total number of identified APC subunits to 13 in both yeasts and indicate that previous approaches were biased against the identification of small subunits. These results underscore the power of direct analysis of protein complexes by mass spectrometry and set the foundation for further functional and structural studies of the APC.
引用
收藏
页码:2048 / 2054
页数:7
相关论文
共 32 条
[1]   A novel Cdc20-related WD-repeat protein, Fzr1, is required for spore formation in Schizosaccharomyces pombe [J].
Asakawa, H ;
Kitamura, K ;
Shimoda, C .
MOLECULAR GENETICS AND GENOMICS, 2001, 265 (03) :424-435
[2]   TATA BOX MUTATIONS IN THE SCHIZOSACCHAROMYCES-POMBE NMT-1 PROMOTER AFFECT TRANSCRIPTION EFFICIENCY BUT NOT THE TRANSCRIPTION START POINT OR THIAMINE REPRESSIBILITY [J].
BASI, G ;
SCHMID, E ;
MAUNDRELL, K .
GENE, 1993, 123 (01) :131-136
[3]  
Berry LD, 1999, MOL CELL BIOL, V19, P2535
[4]  
Blanco MA, 2001, J CELL SCI, V114, P2135
[5]   Study of cyclin proteolysis in anaphase-promoting complex (APC) mutant cells reveals the requirement for APC function in the final steps of the fission yeast septation initiation network [J].
Chang, L ;
Morrell, JL ;
Feoktistova, A ;
Gould, KL .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (19) :6681-6694
[6]   The transcriptional program of sporulation in budding yeast [J].
Chu, S ;
DeRisi, J ;
Eisen, M ;
Mulholland, J ;
Botstein, D ;
Brown, PO ;
Herskowitz, I .
SCIENCE, 1998, 282 (5389) :699-705
[7]   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
[8]   Ama1p is a meiosis-specific regulator of the anaphase promoting complex/cyclosome in yeast [J].
Cooper, KF ;
Mallory, MJ ;
Egeland, DB ;
Jarnik, M ;
Strich, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14548-14553
[9]   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
[10]   A conditional lethal mutant in the fission yeast 26 S protease subunit mts3(+) is defective in metaphase to anaphase transition [J].
Gordon, C ;
McGurk, G ;
Wallace, M ;
Hastie, ND .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (10) :5704-5711