4.8 Article

Sld7, an Sld3-associated protein required for efficient chromosomal DNA replication in budding yeast

期刊

EMBO JOURNAL
卷 30, 期 10, 页码 2019-2030

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/emboj.2011.115

关键词

Cdc45; cell cycle; DNA replication; Sld3; yeast

资金

  1. CREST
  2. Ministry of Education, Culture, Sports, Science and Technology
  3. Grants-in-Aid for Scientific Research [20114006, 20227004] Funding Source: KAKEN

向作者/读者索取更多资源

Genetic screening of yeast for sld (synthetic lethality with dpb11) mutations has identified replication proteins, including Sld2, -3, and -5, and clarified the molecular mechanisms underlying eukaryotic chromosomal DNA replication. Here, we report a new replication protein, Sld7, identified by rescreening of sld mutations. Throughout the cell cycle, Sld7 forms a complex with Sld3, which associates with replication origins in a complex with Cdc45, binds to Dpb11 when phosphorylated by cyclin-dependent kinase, and dissociates from origins once DNA replication starts. However, Sld7 does not move with the replication fork. Sld7 binds to the nonessential N-terminal portion of Sld3 and reduces its affinity for Cdc45, a component of the replication fork. Although Sld7 is not essential for cell growth, its absence reduces the level of cellular Sld3, delays the dissociation from origins of GINS, a component of the replication fork, and slows S-phase progression. These results suggest that Sld7 is required for the proper function of Sld3 at the initiation of DNA replication. The EMBO Journal (2011) 30, 2019-2030. doi: 10.1038/emboj.2011.115; Published online 12 April 2011

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据