Rowntree Rebecca K, Lee Jeannie T
Howard Hughes Medical Institute, Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Mol Cell Biol. 2006 May;26(10):3707-17. doi: 10.1128/MCB.26.10.3707-3717.2006.
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.
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。