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DNA复制起点与X染色体失活中心非编码基因的定位

Mapping of DNA replication origins to noncoding genes of the X-inactivation center.

作者信息

Rowntree Rebecca K, Lee Jeannie T

机构信息

Howard Hughes Medical Institute, Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.

出版信息

Mol Cell Biol. 2006 May;26(10):3707-17. doi: 10.1128/MCB.26.10.3707-3717.2006.

Abstract

In mammals, few DNA replication origins have been identified. Although there appears to be an association between origins and epigenetic regulation, their underlying link to monoallelic gene expression remains unclear. Here, we identify novel origins of DNA replication (ORIs) within the X-inactivation center (Xic). We analyze 86 kb of the Xic using an unbiased approach and find an unexpectedly large number of functional ORIs. Although there has been a tight correlation between ORIs and CpG islands, we find that ORIs are not restricted to CpG islands and there is no dependence on transcriptional activity. Interestingly, these ORIs colocalize to important genetic elements or genes involved in X-chromosome inactivation. One prominent ORI maps to the imprinting center and to a domain within Tsix known to be required for X-chromosome counting and choice. Location and/or activity of ORIs appear to be modulated by removal of specific Xic elements. These data provide a foundation for testing potential relationships between DNA replication and epigenetic regulation in future studies.

摘要

在哺乳动物中,已鉴定出的DNA复制起点很少。尽管起点与表观遗传调控之间似乎存在关联,但其与单等位基因表达的潜在联系仍不清楚。在这里,我们在X染色体失活中心(Xic)内鉴定出了新的DNA复制起点(ORIs)。我们采用无偏倚方法分析了86 kb的Xic,发现了数量出乎意料的功能性ORIs。尽管ORIs与CpG岛之间存在紧密的相关性,但我们发现ORIs并不局限于CpG岛,且不依赖于转录活性。有趣的是,这些ORIs与参与X染色体失活的重要遗传元件或基因共定位。一个突出的ORI定位于印记中心以及已知在X染色体计数和选择中必需的Tsix内的一个结构域。ORIs的位置和/或活性似乎会因特定Xic元件的去除而受到调节。这些数据为未来研究中测试DNA复制与表观遗传调控之间的潜在关系奠定了基础。

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本文引用的文献

2
Regulation of X-chromosome counting by Tsix and Xite sequences.
Science. 2005 Jul 29;309(5735):768-71. doi: 10.1126/science.1113673.
3
Identification of developmentally specific enhancers for Tsix in the regulation of X chromosome inactivation.
Mol Cell Biol. 2005 Apr;25(7):2757-69. doi: 10.1128/MCB.25.7.2757-2769.2005.
4
X chromosome choice occurs independently of asynchronous replication timing.
J Cell Biol. 2005 Jan 31;168(3):365-73. doi: 10.1083/jcb.200405117. Epub 2005 Jan 24.
5
Cell cycle and developmental regulations of replication factors in mouse embryonic stem cells.
J Biol Chem. 2005 Apr 1;280(13):12976-87. doi: 10.1074/jbc.M412224200. Epub 2005 Jan 19.
6
7
In search of the holy replicator.
Nat Rev Mol Cell Biol. 2004 Oct;5(10):848-55. doi: 10.1038/nrm1495.
8
Chromatin regulates origin activity in Drosophila follicle cells.
Nature. 2004 Jul 15;430(6997):372-6. doi: 10.1038/nature02694.
9
Specification of a DNA replication origin by a transcription complex.
Nat Cell Biol. 2004 Aug;6(8):721-30. doi: 10.1038/ncb1149. Epub 2004 Jul 11.
10
Initiation sites for human DNA replication at a putative ribulose-5-phosphate 3-epimerase gene.
Biochem Biophys Res Commun. 2004 Jul 30;320(3):648-55. doi: 10.1016/j.bbrc.2004.06.018.

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