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本文引用的文献

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BRG1 co-localizes with DNA replication factors and is required for efficient replication fork progression.BRG1 与 DNA 复制因子共定位,并且对于有效的复制叉推进是必需的。
Nucleic Acids Res. 2010 Nov;38(20):6906-19. doi: 10.1093/nar/gkq559. Epub 2010 Jun 22.
3
Abasic sites preferentially form at regions undergoing DNA replication.堿基部位易在进行 DNA 复制的区域形成。
FASEB J. 2010 Oct;24(10):3674-80. doi: 10.1096/fj.09-145276. Epub 2010 May 28.
4
Predictable dynamic program of timing of DNA replication in human cells.人类细胞中 DNA 复制时间的可预测动态程序。
Genome Res. 2009 Dec;19(12):2288-99. doi: 10.1101/gr.094060.109. Epub 2009 Sep 18.
5
Temporal differences in DNA replication during the S phase using single fiber analysis of normal human fibroblasts and glioblastoma T98G cells.用正常人成纤维细胞和神经胶质瘤 T98G 细胞的单纤维分析方法研究 S 期 DNA 复制的时间差异。
Cell Cycle. 2009 Oct 1;8(19):3133-48. doi: 10.4161/cc.8.19.9682.
6
DNA replication and the GINS complex: localization on extended chromatin fibers.DNA 复制与 GINS 复合物:在延伸的染色质纤维上的定位。
Epigenetics Chromatin. 2009 May 14;2(1):6. doi: 10.1186/1756-8935-2-6.
7
Replication timing as an epigenetic mark.复制时间作为一种表观遗传标记。
Epigenetics. 2009 Feb 16;4(2):93-7. doi: 10.4161/epi.4.2.7772. Epub 2009 Feb 1.
8
Excess MCM proteins protect human cells from replicative stress by licensing backup origins of replication.过量的微小染色体维持缺陷蛋白通过许可备用复制起点来保护人类细胞免受复制应激。
Proc Natl Acad Sci U S A. 2008 Jul 1;105(26):8956-61. doi: 10.1073/pnas.0803978105. Epub 2008 Jun 25.
9
DNA replication in early S phase pauses near newly activated origins.在S期早期,DNA复制在新激活的起始点附近暂停。
Cell Cycle. 2008 May 15;7(10):1440-8. doi: 10.4161/cc.7.10.5879. Epub 2008 Feb 29.
10
Dormant origins licensed by excess Mcm2-7 are required for human cells to survive replicative stress.由过量的Mcm2-7许可的休眠起源对于人类细胞在复制应激下存活是必需的。
Genes Dev. 2007 Dec 15;21(24):3331-41. doi: 10.1101/gad.457807.

对在S期早期复制的DNA进行时间和功能分析。

Temporal and functional analysis of DNA replicated in early S phase.

作者信息

Kaufman David G, Cohen Stephanie M, Chastain Paul D

机构信息

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Adv Enzyme Regul. 2011;51(1):257-71. doi: 10.1016/j.advenzreg.2010.11.004. Epub 2010 Nov 18.

DOI:10.1016/j.advenzreg.2010.11.004
PMID:21093474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3079056/
Abstract

In summary, recently developed technologies have begun to draw back the curtain of mystery that obscures some of the basic mechanisms of DNA replication at multiple levels. Studies using extended DNA and chromatin fiber techniques have proven valuable for identifying the location of origins of replication at specific genomic sites and determining their temporal order of replication, for identifying and quantifying sites of DNA damage and localizing chromatin proteins in relation to sites of DNA replication. The future potential of these methods include further discoveries in functional genomics and contributions to the elucidation of the histone code. Such studies could prove very valuable in studies of the mechanisms of cancer development, aging, and other processes of disordered genomic functioning.

摘要

总之,最近开发的技术已开始揭开笼罩在DNA复制某些基本机制上的多层神秘面纱。使用延伸DNA和染色质纤维技术的研究已证明在确定特定基因组位点的复制起点位置、确定其复制时间顺序、识别和量化DNA损伤位点以及确定与DNA复制位点相关的染色质蛋白定位方面具有重要价值。这些方法未来的潜力包括在功能基因组学方面的进一步发现以及对阐明组蛋白密码的贡献。此类研究在癌症发展、衰老及其他基因组功能紊乱过程的机制研究中可能极具价值。