Department of Biological Science, Florida State University, Tallahassee, Florida, United States of America.
PLoS One. 2012;7(11):e50023. doi: 10.1371/journal.pone.0050023. Epub 2012 Nov 14.
Replicating the genome prior to each somatic cell division not only requires precise duplication of the genetic information, but also accurately reestablishing the epigenetic signatures that instruct how the genetic material is to be interpreted in the daughter cells. The mammalian inactive X chromosome (Xi), which is faithfully inherited in a silent state in each daughter cell, provides an excellent model of epigenetic regulation. While much is known about the early stages of X chromosome inactivation, much less is understood with regards to retaining the Xi chromatin through somatic cell division. Here we report that the WSTF-ISWI chromatin remodeling complex (WICH) associates with the Xi during late S-phase as the Xi DNA is replicated. Elevated levels of WICH at the Xi is restricted to late S-phase and appears before BRCA1 and γ-H2A.X. The sequential appearance of WICH and BRCA1/γ-H2A.X implicate each as performing important but distinct roles in the maturation and maintenance of heterochromatin at the Xi.
在每个体细胞分裂之前复制基因组不仅需要精确复制遗传信息,还需要准确地重新建立指导遗传物质在子细胞中如何被解释的表观遗传特征。哺乳动物失活 X 染色体(Xi)在每个子细胞中以沉默状态被忠实遗传,为表观遗传调控提供了一个极好的模型。虽然人们对 X 染色体失活的早期阶段有了很多了解,但对于如何在体细胞分裂过程中保持 Xi 染色质知之甚少。在这里,我们报告说,WSTF-ISWI 染色质重塑复合物(WICH)在 S 期晚期与 Xi 结合,因为 Xi DNA 正在复制。Xi 上 WICH 的高水平仅局限于 S 期晚期,并且出现在 BRCA1 和 γ-H2A.X 之前。WICH 和 BRCA1/γ-H2A.X 的顺序出现表明它们在 Xi 上异染色质的成熟和维持中都具有重要但不同的作用。