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酿酒酵母的G1期特异性细胞周期蛋白:细胞周期的周期性、交配信息素的调控以及与p34CDC28蛋白激酶的关联

G1-specific cyclins of S. cerevisiae: cell cycle periodicity, regulation by mating pheromone, and association with the p34CDC28 protein kinase.

作者信息

Wittenberg C, Sugimoto K, Reed S I

机构信息

Department of Molecular Biology, Research Institute of Scripps Clinic, La Jolla, California 92037.

出版信息

Cell. 1990 Jul 27;62(2):225-37. doi: 10.1016/0092-8674(90)90361-h.

Abstract

The S. cerevisiae CLN genes encode cyclin homologs essential for progression from G1 to S phase. The CLN2 gene encodes a 62 kd polypeptide that accumulates periodically, peaking during G1 and decreasing rapidly thereafter, and is rapidly lost following exposure of cells to mating pheromone. Cln2 abundance can be explained by the G1-specific accumulation of the CLN2 transcript coupled with instability of the Cln2 protein. The abundance of the CLN1 and CLN2 transcripts increases greater than 5-fold during the G1 interval, decreasing dramatically as cells enter S phase. Both transcripts decrease in cells responding to mating pheromone. Finally, we demonstrate that the Cln2 polypeptide interacts with p34CDC28 to form an active protein kinase complex. This physical interaction is consistent with the genetic interaction between the CLN genes and CDC28 and suggests that Cln proteins are an essential component of the active protein kinase complex required for the G1 to S transition.

摘要

酿酒酵母的CLN基因编码细胞周期蛋白同源物,对于从G1期进入S期的进程至关重要。CLN2基因编码一种62kd的多肽,该多肽周期性积累,在G1期达到峰值,此后迅速下降,并且在细胞暴露于交配信息素后迅速消失。Cln2的丰度可以通过CLN2转录本在G1期特异性积累以及Cln2蛋白的不稳定性来解释。在G1期间隔期间,CLN1和CLN2转录本的丰度增加超过5倍,随着细胞进入S期而急剧下降。在对交配信息素作出反应的细胞中,两种转录本都减少。最后,我们证明Cln2多肽与p34CDC28相互作用形成活性蛋白激酶复合物。这种物理相互作用与CLN基因和CDC28之间的遗传相互作用一致,并表明Cln蛋白是G1期到S期转换所需的活性蛋白激酶复合物的重要组成部分。

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