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转录复合物对DNA复制起点的特异性决定

Specification of a DNA replication origin by a transcription complex.

作者信息

Danis Etienne, Brodolin Konstantin, Menut Sophie, Maiorano Domenico, Girard-Reydet Claire, Méchali Marcel

机构信息

Institute of Human Genetics, CNRS, Genome Dynamics and Development, 141 rue de la Cardonille, 34396 Montpellier Cedex 5, France.

出版信息

Nat Cell Biol. 2004 Aug;6(8):721-30. doi: 10.1038/ncb1149. Epub 2004 Jul 11.

Abstract

In early Xenopus development, transcription is repressed and DNA replication initiates at non-specific sites. Here, we show that a site-specific DNA replication origin can be induced in this context by the assembly of a transcription domain. Deletion of the promoter element abolishes site-specific initiation, and its relocalization to an ectopic site induces a new origin of replication. This process does not require active transcription, and specification of the origin occurs mainly through a decrease in non-specific initiation at sites distant from the promoter. Finally, chromatin immunoprecipitation experiments suggest that site-specific acetylation of histones favours the selection of the active DNA replication origin. We propose that the specification of active DNA replication origins occurs by secondary epigenetic events and that the programming of chromatin for transcription during development contributes to this selection in higher eukaryotes.

摘要

在非洲爪蟾早期发育过程中,转录受到抑制,DNA复制在非特异性位点起始。在此,我们表明在这种情况下,通过转录结构域的组装可诱导出位点特异性DNA复制起点。启动子元件的缺失消除了位点特异性起始,而将其重新定位到异位位点会诱导产生新的复制起点。这一过程不需要活跃转录,并且复制起点的确定主要是通过远离启动子位点的非特异性起始减少来实现的。最后,染色质免疫沉淀实验表明,组蛋白的位点特异性乙酰化有利于活性DNA复制起点的选择。我们提出,活性DNA复制起点的确定是由次级表观遗传事件发生的,并且发育过程中染色质的转录编程有助于高等真核生物中的这种选择。

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