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Cdc2对Cdc18 DNA复制蛋白的负调控

Negative regulation of Cdc18 DNA replication protein by Cdc2.

作者信息

Lopez-Girona A, Mondesert O, Leatherwood J, Russell P

机构信息

Departments of Molecular Biology and Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

Mol Biol Cell. 1998 Jan;9(1):63-73. doi: 10.1091/mbc.9.1.63.

Abstract

Fission yeast Cdc18, a homologue of Cdc6 in budding yeast and metazoans, is periodically expressed during the S phase and required for activation of replication origins. Cdc18 overexpression induces DNA rereplication without mitosis, as does elimination of Cdc2-Cdc13 kinase during G2 phase. These findings suggest that illegitimate activation of origins may be prevented through inhibition of Cdc18 by Cdc2. Consistent with this hypothesis, we report that Cdc18 interacts with Cdc2 in association with Cdc13 and Cig2 B-type cyclins in vivo. Cdc18 is phosphorylated by the associated Cdc2 in vitro. Mutation of a single phosphorylation site, T104A, activates Cdc18 in the rereplication assay. The cdc18-K9 mutation is suppressed by a cig2 mutation, providing genetic evidence that Cdc2-Cig2 kinase inhibits Cdc18. Moreover, constitutive expression of Cig2 prevents rereplication in cells lacking Cdc13. These findings identify Cdc18 as a key target of Cdc2-Cdc13 and Cdc2-Cig2 kinases in the mechanism that limits chromosomal DNA replication to once per cell cycle.

摘要

裂殖酵母Cdc18是芽殖酵母和后生动物中Cdc6的同源物,在S期周期性表达,是复制起点激活所必需的。Cdc18过表达会诱导DNA在没有有丝分裂的情况下重新复制,G2期消除Cdc2-Cdc13激酶时也会出现这种情况。这些发现表明,通过Cdc2抑制Cdc18可能会阻止复制起点的非法激活。与这一假设一致,我们报道Cdc18在体内与Cdc2以及Cdc13和Cig2 B型细胞周期蛋白相互作用。Cdc18在体外被相关的Cdc2磷酸化。单个磷酸化位点T104A的突变在重新复制试验中激活了Cdc18。cdc18-K9突变被cig2突变抑制,提供了Cdc2-Cig2激酶抑制Cdc18的遗传学证据。此外,Cig2的组成型表达可防止缺乏Cdc13的细胞中出现重新复制。这些发现确定Cdc18是Cdc2-Cdc13和Cdc2-Cig2激酶在将染色体DNA复制限制在每个细胞周期一次的机制中的关键靶点。

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