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一种含果蝇Myb蛋白复合物在位点特异性DNA复制中的作用。

Role for a Drosophila Myb-containing protein complex in site-specific DNA replication.

作者信息

Beall Eileen L, Manak J Robert, Zhou Sharleen, Bell Maren, Lipsick Joseph S, Botchan Michael R

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.

出版信息

Nature. 2002;420(6917):833-7. doi: 10.1038/nature01228.

Abstract

There is considerable interest in the developmental, temporal and tissue-specific patterns of DNA replication in metazoans. Site-specific DNA replication at the chorion loci in Drosophila follicle cells leads to extensive gene amplification, and the organization of the cis-acting DNA elements that regulate this process may provide a model for how such regulation is achieved. Two elements important for amplification of the third chromosome chorion gene cluster, ACE3 and Ori-beta, are directly bound by Orc (origin recognition complex), and two-dimensional gel analysis has revealed that the primary origin used is Ori-beta (refs 7-9). Here we show that the Drosophila homologue of the Myb (Myeloblastosis) oncoprotein family is tightly associated with four additional proteins, and that the complex binds site-specifically to these regulatory DNA elements. Drosophila Myb is required in trans for gene amplification, showing that a Myb protein is directly involved in DNA replication. A Drosophila Myb binding site, as well as the binding site for another Myb complex member (p120), is necessary in cis for replication of reporter transgenes. Chromatin immunoprecipitation experiments localize both proteins to the chorion loci in vivo. These data provide evidence that specific protein complexes bound to replication enhancer elements work together with the general replication machinery for site-specific origin utilization during replication.

摘要

后生动物DNA复制的发育、时间和组织特异性模式受到了广泛关注。果蝇卵泡细胞中绒毛膜基因座的位点特异性DNA复制导致广泛的基因扩增,而调节这一过程的顺式作用DNA元件的组织方式可能为实现这种调节提供一个模型。对第三染色体绒毛膜基因簇扩增重要的两个元件ACE3和Ori-β直接与Orc(起始识别复合物)结合,二维凝胶分析表明所使用的主要起始位点是Ori-β(参考文献7-9)。在这里,我们表明成髓细胞瘤(Myeloblastosis)癌蛋白家族的果蝇同源物与另外四种蛋白质紧密相关,并且该复合物位点特异性地结合这些调节性DNA元件。果蝇Myb在反式作用中是基因扩增所必需的,这表明Myb蛋白直接参与DNA复制。果蝇Myb结合位点以及另一个Myb复合物成员(p120)的结合位点在顺式作用中是报告转基因复制所必需的。染色质免疫沉淀实验在体内将这两种蛋白质定位到绒毛膜基因座。这些数据提供了证据,表明与复制增强子元件结合的特定蛋白质复合物与一般复制机制共同作用,以在复制过程中实现位点特异性起始位点的利用。

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