首页> 外文期刊>Nucleic Acids Research >The dhfr oribeta-binding protein RIP60 contains 15 zinc fingers: DNA binding and looping by the central three fingers and an associated proline-rich region.
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The dhfr oribeta-binding protein RIP60 contains 15 zinc fingers: DNA binding and looping by the central three fingers and an associated proline-rich region.

机译:dhfr oribeta结合蛋白RIP60包含15个锌指:三个中指和一个相关的富含脯氨酸的区域与DNA结合和环化。

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摘要

Initiation of DNA replication occurs with high frequency within oribeta, a short region 3' to the Chinese hamster dhfr gene. Homodimers of RIP60 (replication initiation-region protein 60 kDA) purified from nuclear extract bind two ATT-rich sites in oribeta and foster the formation of a twisted 720 bp DNA loop in vitro. Using a one hybrid screen in yeast, we have cloned the cDNA for human RIP60. RIP60 contains 15 C(2)H(2)zinc finger (ZF) DNA binding motifs organized in three clusters, termed hand Z1 (ZFs 1-5), hand Z2 (ZFs 6-8) and hand Z3 (ZFs 9-15). A proline-rich region is located between hands Z2 and Z3. Gel mobility shift and DNase I footprinting experiments show hands Z1 and Z2 independently bind the oribeta RIP60 sites specifically, but with different affinities. Hand Z3 binds DNA, but displays no specificity for RIP60 sites. Ligation enhancement, DNase I footprinting, and atomic force microscopy assays show that hand Z2 and a portion of the associated proline-rich region is sufficient for protein multimerization on DNA and DNA looping in vitro. Polyomavirus origin-dependent plasmid replication assays show RIP60 has weak replication enhancer activity, suggesting that RIP60 does not harbor a transcriptional transactivation domain. Because vertebrate origins of replication have no known consensus sequence, we suggest that sequence-specific DNA binding proteins such as RIP60 may act as accessory factors in origin identification prior to the assembly of pre-initiation complexes.
机译:DNA复制的启动在oribeta(中国仓鼠dhfr基因的3'短区域)内高频率发生。从核提取物中纯化的RIP60(复制起始区蛋白60 kDA)的同型物与oribeta中的两个ATT富集位点结合,并在体外促进扭曲的720 bp DNA环的形成。使用酵母中的一个杂交筛选,我们已经克隆了人RIP60的cDNA。 RIP60包含15个C(2)H(2)锌指(ZF)DNA结合基序,分为三个簇,称为手Z1(ZF 1-5),手Z2(ZF 6-8)和手Z3(ZF 9-15) )。富含脯氨酸的区域位于手Z2和Z3之间。凝胶迁移率变化和DNase I足迹实验表明,手Z1和Z2独立地特异性结合oribeta RIP60位点,但亲和力不同。 Z3手与DNA结合,但对RIP60位点没有特异性。连接增强,DNase I足迹和原子力显微镜分析表明,手Z2和部分相关的脯氨酸富集区域足以在体外DNA和DNA环上进行蛋白质多聚。多瘤病毒起源依赖性质粒复制试验表明,RIP60具有弱的复制增强子活性,表明RIP60不具有转录反式激活结构域。因为脊椎动物的复制起点没有已知的共有序列,所以我们建议在组装预启动复合物之前,序列特异性DNA结合蛋白(例如RIP60)可能会作为起点鉴定中的辅助因子。

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