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GINS是一种在芽殖酵母中进行染色体DNA复制所需的新型多蛋白复合物。

GINS, a novel multiprotein complex required for chromosomal DNA replication in budding yeast.

作者信息

Takayama Yuko, Kamimura Yoichiro, Okawa Mariko, Muramatsu Sachiko, Sugino Akio, Araki Hiroyuki

机构信息

Division of Microbial Genetics, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan.

出版信息

Genes Dev. 2003 May 1;17(9):1153-65. doi: 10.1101/gad.1065903.

Abstract

Eukaryotic chromosomal DNA replication requires a two-step assembly of replication proteins on origins; formation of the prereplicative complex (pre-RC) in late M and G1 phases of the cell cycle, and assembly of other replication proteins in S phase to load DNA polymerases to initiate DNA synthesis. In budding yeast, assembly of Dpb11 and the Sld3-Cdc45 complex on the pre-RC at origins is required for loading DNA polymerases. Here we describe a novel replication complex, GINS (Go, Ichi, Nii, and San; five, one, two, and three in Japanese), in budding yeast, consisting of Sld5, Psf1 (partner of Sld five 1), Psf2, and Psf3 proteins, all of which are highly conserved in eukaryotic cells. Since the conditional mutations of Sld5 and Psf1 confer defect of DNA replication under nonpermissive conditions, GINS is suggested to function for chromosomal DNA replication. Consistently, in S phase, GINS associates first with replication origins and then with neighboring sequences. Without GINS, neither Dpb11 nor Cdc45 associates properly with chromatin DNA. Conversely, without Dpb11 or Sld3, GINS does not associate with origins. Moreover, genetic and two-hybrid interactions suggest that GINS interacts with Sld3 and Dpb11. Therefore, Dpb11, Sld3, Cdc45, and GINS assemble in a mutually dependent manner on replication origins to initiate DNA synthesis.

摘要

真核染色体DNA复制需要在复制起点上分两步组装复制蛋白:在细胞周期的M期晚期和G1期形成前复制复合体(pre-RC),并在S期组装其他复制蛋白以加载DNA聚合酶来启动DNA合成。在芽殖酵母中,Dpb11和Sld3-Cdc45复合体在复制起点的pre-RC上组装是加载DNA聚合酶所必需的。在此,我们描述了芽殖酵母中的一种新型复制复合体GINS(Go、Ichi、Nii和San;在日语中分别为五、一、二和三),它由Sld5、Psf1(Sld five 1的伙伴)、Psf2和Psf3蛋白组成,所有这些蛋白在真核细胞中都高度保守。由于Sld5和Psf1的条件性突变在非允许条件下导致DNA复制缺陷,因此推测GINS在染色体DNA复制中发挥作用。一致的是,在S期,GINS首先与复制起点结合,然后与相邻序列结合。没有GINS,Dpb11和Cdc45都不能正确地与染色质DNA结合。相反,没有Dpb11或Sld3,GINS就不会与复制起点结合。此外,遗传学和双杂交相互作用表明GINS与Sld3和Dpb11相互作用。因此,Dpb11、Sld3、Cdc45和GINS以相互依赖的方式在复制起点组装以启动DNA合成。

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