CDC16P, CDC23P AND CDC27P FORM A COMPLEX ESSENTIAL FOR MITOSIS

被引:221
作者
LAMB, JR
MICHAUD, WA
SIKORSKI, RS
HIETER, PA
机构
[1] Department of Molecular Biology, Johns Hopkins University, School of Medicine, Baltimore, MD 21205
[2] Department of Biological Sciences, Univ. of Maryland, Baltimore County, Catonsville
关键词
CDC16; CDC23; CDC27; CELL CYCLE; MITOSIS; PROTEIN-PROTEIN INTERACTIONS; TPR;
D O I
10.1002/j.1460-2075.1994.tb06752.x
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
Cdc16p, Cdc23p and Cdc27p are all essential proteins required for cell cycle progression through mitosis in Saccharomyces cerevisiae. All three proteins contain multiple tandemly repeated 34 amino acid tetratrico-peptide repeats (TPRs). Using two independent assays, two-hybrid analysis in vivo and co-immunoprecipitation in vitro, we demonstrate that Cdc16p, Cdc23p and Cdc27p self associate and interact with one another to form a macromolecular complex. A temperature sensitive mutation in the most highly conserved TPR domain of Cdc27p results in a greatly reduced ability to interact with Cdc23p, but has no effect on interactions with wild-type Cdc27p or Cdc16p. The specificity of this effect indicates that TPRs can mediate protein-protein interactions and that this mutation may define an essential interaction for cell cycle progression in yeast. The conservation of at least two of the three proteins from yeast to man suggests that this protein complex is essential for mitosis in a wide range of eukaryotes.
引用
收藏
页码:4321 / 4328
页数:8
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