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本文引用的文献

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The G4 genome.G4基因组。
PLoS Genet. 2013 Apr;9(4):e1003468. doi: 10.1371/journal.pgen.1003468. Epub 2013 Apr 18.
2
Co-transcriptional formation of DNA:RNA hybrid G-quadruplex and potential function as constitutional cis element for transcription control.DNA:RNA 杂交 G-四链体的共转录形成及其作为转录调控的组成性顺式元件的潜在功能。
Nucleic Acids Res. 2013 May 1;41(10):5533-41. doi: 10.1093/nar/gkt264. Epub 2013 Apr 12.
3
Genome-wide mapping of human DNA-replication origins: levels of transcription at ORC1 sites regulate origin selection and replication timing.人类 DNA 复制起始点的全基因组图谱绘制:ORC1 位点的转录水平调节着起始点选择和复制时间。
Genome Res. 2013 Jan;23(1):1-11. doi: 10.1101/gr.142331.112. Epub 2012 Nov 27.
4
Unraveling cell type-specific and reprogrammable human replication origin signatures associated with G-quadruplex consensus motifs.解析与 G-四链体共识基序相关的具有细胞类型特异性和可重编程性的人类复制起始点特征。
Nat Struct Mol Biol. 2012 Aug;19(8):837-44. doi: 10.1038/nsmb.2339. Epub 2012 Jul 1.
5
Epstein-Barr nuclear antigen 1 (EBNA1)-dependent recruitment of origin recognition complex (Orc) on oriP of Epstein-Barr virus with purified proteins: stimulation by Cdc6 through its direct interaction with EBNA1. Epstein-Barr 核抗原 1(EBNA1)依赖性募集起始识别复合物(Orc)在 Epstein-Barr 病毒 oriP 上的纯蛋白:通过 Cdc6 与其与 EBNA1 的直接相互作用的刺激。
J Biol Chem. 2012 Jul 6;287(28):23977-94. doi: 10.1074/jbc.M112.368456. Epub 2012 May 14.
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R loops: from transcription byproducts to threats to genome stability.R 环:从转录副产物到基因组稳定性的威胁。
Mol Cell. 2012 Apr 27;46(2):115-24. doi: 10.1016/j.molcel.2012.04.009.
7
New insights into replication origin characteristics in metazoans.真核生物复制起始点特征的新认识。
Cell Cycle. 2012 Feb 15;11(4):658-67. doi: 10.4161/cc.11.4.19097.
8
Genome-wide depletion of replication initiation events in highly transcribed regions.全基因组范围内高度转录区域的复制起始事件耗竭。
Genome Res. 2011 Nov;21(11):1822-32. doi: 10.1101/gr.124644.111. Epub 2011 Aug 3.
9
Genome-scale analysis of metazoan replication origins reveals their organization in specific but flexible sites defined by conserved features.真核生物复制起点的全基因组分析揭示了它们在特定但灵活的位点的组织,这些位点由保守特征定义。
Genome Res. 2011 Sep;21(9):1438-49. doi: 10.1101/gr.121830.111. Epub 2011 Jul 12.
10
Preferential localization of human origins of DNA replication at the 5'-ends of expressed genes and at evolutionarily conserved DNA sequences.人类 DNA 复制起点优先定位于表达基因的 5' 端和进化上保守的 DNA 序列。
PLoS One. 2011;6(5):e17308. doi: 10.1371/journal.pone.0017308. Epub 2011 May 13.

人源识别复合物优先结合于 G-四链体偏好的 RNA 和单链 DNA。

Human origin recognition complex binds preferentially to G-quadruplex-preferable RNA and single-stranded DNA.

机构信息

From the Department of Chemical and Biological Sciences, Faculty of Science, Japan Women's University, Tokyo 112-8681, Japan.

the Graduate School of Humanities and Sciences, Ochanomizu University, Tokyo 112-8610, Japan.

出版信息

J Biol Chem. 2013 Oct 18;288(42):30161-30171. doi: 10.1074/jbc.M113.492504. Epub 2013 Sep 3.

DOI:10.1074/jbc.M113.492504
PMID:24003239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3798484/
Abstract

Origin recognition complex (ORC), consisting of six subunits ORC1-6, is known to bind to replication origins and function in the initiation of DNA replication in eukaryotic cells. In contrast to the fact that Saccharomyces cerevisiae ORC recognizes the replication origin in a sequence-specific manner, metazoan ORC has not exhibited strict sequence-specificity for DNA binding. Here we report that human ORC binds preferentially to G-quadruplex (G4)-preferable G-rich RNA or single-stranded DNA (ssDNA). We mapped the G-rich RNA-binding domain in the ORC1 subunit, in a region adjacent to its ATPase domain. This domain itself has an ability to preferentially recognize G4-preferable sequences of ssDNA. Furthermore, we found, by structure modeling, that the G-rich RNA-binding domain is similar to the N-terminal portion of AdoMet_MTase domain of mammalian DNA methyltransferase 1. Therefore, in contrast with the binding to double-stranded DNA, human ORC has an apparent sequence preference with respect to its RNA/ssDNA binding. Interestingly, this specificity coincides with the common signature present in most of the human replication origins. We expect that our findings provide new insights into the regulations of function and chromatin binding of metazoan ORCs.

摘要

起始识别复合物(ORC)由六个亚基 ORC1-6 组成,已知其与复制起始点结合,并在真核细胞中启动 DNA 复制。与酿酒酵母 ORC 以序列特异性方式识别复制起始点的事实相反,真核生物 ORC 对 DNA 结合没有表现出严格的序列特异性。在这里,我们报告人类 ORC 优先结合 G-四联体(G4)偏好性 G 丰富 RNA 或单链 DNA(ssDNA)。我们在 ORC1 亚基中定位了 G 丰富 RNA 结合域,该域位于其 ATP 酶结构域附近。该结构域本身具有优先识别 G4 偏好性 ssDNA 序列的能力。此外,我们通过结构建模发现,G 丰富 RNA 结合域与哺乳动物 DNA 甲基转移酶 1 的 AdoMet_MTase 结构域的 N 端部分相似。因此,与结合双链 DNA 相比,人类 ORC 对其 RNA/ssDNA 结合具有明显的序列偏好性。有趣的是,这种特异性与大多数人类复制起始点存在的共同特征一致。我们预计我们的发现将为真核生物 ORC 的功能调控和染色质结合提供新的见解。