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本文引用的文献

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DNA secondary structures and epigenetic determinants of cancer genome evolution.DNA 二级结构和癌症基因组进化的表观遗传决定因素。
Nat Struct Mol Biol. 2011 Jul 3;18(8):950-5. doi: 10.1038/nsmb.2089.
2
DNA replication through G-quadruplex motifs is promoted by the Saccharomyces cerevisiae Pif1 DNA helicase.酵母 Pif1 DNA 解旋酶促进 G-四链体基序的 DNA 复制。
Cell. 2011 May 27;145(5):678-91. doi: 10.1016/j.cell.2011.04.015.
3
Rudimentary G-quadruplex-based telomere capping in Saccharomyces cerevisiae.酿酒酵母中基于原始 G-四链体的端粒封闭。
Nat Struct Mol Biol. 2011 Apr;18(4):478-85. doi: 10.1038/nsmb.2033. Epub 2011 Mar 13.
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Massive genomic rearrangement acquired in a single catastrophic event during cancer development.在癌症发展过程中,单一灾难性事件获得的大规模基因组重排。
Cell. 2011 Jan 7;144(1):27-40. doi: 10.1016/j.cell.2010.11.055.
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Stability of telomeric G-quadruplexes.端粒 G-四链体的稳定性。
Nucleic Acids Res. 2011 Apr;39(8):3282-94. doi: 10.1093/nar/gkq1292. Epub 2010 Dec 21.
6
Epigenetic instability due to defective replication of structured DNA.由于结构 DNA 的复制缺陷导致的表观遗传不稳定。
Mol Cell. 2010 Dec 10;40(5):703-13. doi: 10.1016/j.molcel.2010.11.009.
7
ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner.ATR-X 综合征蛋白靶向串联重复序列,并以大小依赖的方式影响等位基因特异性表达。
Cell. 2010 Oct 29;143(3):367-78. doi: 10.1016/j.cell.2010.09.023.
8
Formation of a G-quadruplex at the BCL2 major breakpoint region of the t(14;18) translocation in follicular lymphoma.滤泡性淋巴瘤中 t(14;18)易位的 BCL2 主要断裂点区域形成 G-四链体。
Nucleic Acids Res. 2011 Feb;39(3):936-48. doi: 10.1093/nar/gkq824. Epub 2010 Sep 29.
9
Replication termination at eukaryotic chromosomes is mediated by Top2 and occurs at genomic loci containing pausing elements.真核染色体的复制终止由 Top2 介导,并发生在含有暂停元件的基因组位点上。
Mol Cell. 2010 Aug 27;39(4):595-605. doi: 10.1016/j.molcel.2010.07.024.
10
G-quadruplex nucleic acids and human disease.G-四链体核酸与人类疾病。
FEBS J. 2010 Sep;277(17):3470-88. doi: 10.1111/j.1742-4658.2010.07760.x. Epub 2010 Jul 29.

G-四链体诱导的先导链复制不稳定。

G-quadruplex-induced instability during leading-strand replication.

机构信息

Recombinaison et Instabilité Génétique, Institut Curie Centre de Recherche, CNRS UMR3244, Université Pierre et Marie Curie, Paris Cedex 05, France.

出版信息

EMBO J. 2011 Aug 26;30(19):4033-46. doi: 10.1038/emboj.2011.316.

DOI:10.1038/emboj.2011.316
PMID:21873979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3209785/
Abstract

G-quadruplexes are four-stranded nucleic acid structures whose biological functions remain poorly understood. In the yeast S. cerevisiae, we report that G-quadruplexes form and, if not properly processed, pose a specific challenge to replication. We show that the G-quadruplex-prone CEB1 tandem array is tolerated when inserted near ARS305 replication origin in wild-type cells but is very frequently destabilized upon treatment with the potent Phen-DC(3) G-quadruplex ligand, or in the absence of the G-quadruplex-unwinding Pif1 helicase, only when the G-rich strand is the template of leading-strand replication. The orientation-dependent instability is associated with the formation of Rad51-Rad52-dependent X-shaped intermediates during replication detected by two-dimensional (2D) gels, and relies on the presence of intact G-quadruplex motifs in CEB1 and on the activity of ARS305. The asymmetrical behaviour of G-quadruplex prone sequences during replication has implications for their evolutionary dynamics within genomes, including the maintenance of G-rich telomeres.

摘要

四链体是由 4 条链组成的核酸结构,其生物学功能仍知之甚少。在酵母 S. cerevisiae 中,我们报告说四链体形成,如果不能正确处理,会对复制造成特殊的挑战。我们表明,当 G 四链体倾向的 CEB1 串联阵列插入到野生型细胞的 ARS305 复制起点附近时是可以容忍的,但在用强 Phen-DC(3) G 四链体配体处理或在没有 G 四链体解旋酶 Pif1 的情况下,只有当富含 G 的链是前导链复制的模板时,它才会非常频繁地不稳定。二维 (2D) 凝胶检测到的复制过程中形成的 Rad51-Rad52 依赖性 X 形中间体与取向依赖性不稳定性有关,并且依赖于 CEB1 中完整的 G 四链体基序和 ARS305 的活性。复制过程中易发生 G 四链体的序列的不对称行为对其在基因组内的进化动态具有重要意义,包括富含 G 的端粒的维持。