Department of Biotechnology, Graduate School of Engineering, Osaka University, Suita 565-0871, Japan.
Cell Rep. 2012 Apr 19;1(4):299-308. doi: 10.1016/j.celrep.2012.02.005. Epub 2012 Mar 22.
Cohesion is essential for the identification of sister chromatids and for the biorientation of chromosomes until their segregation. Here, we have demonstrated that an RNA-binding motif protein encoded on the X chromosome (RBMX) plays an essential role in chromosome morphogenesis through its association with chromatin, but not with RNA. Depletion of RBMX by RNA interference (RNAi) causes the loss of cohesin from the centromeric regions before anaphase, resulting in premature chromatid separation accompanied by delocalization of the shugoshin complex and outer kinetochore proteins. Cohesion defects caused by RBMX depletion can be detected as early as the G2 phase. Moreover, RBMX associates with the cohesin subunits, Scc1 and Smc3, and with the cohesion regulator, Wapl. RBMX is required for cohesion only in the presence of Wapl, suggesting that RBMX is an inhibitor of Wapl. We propose that RBMX is a cohesion regulator that maintains the proper cohesion of sister chromatids.
着丝粒对于姐妹染色单体的识别以及在它们分离之前的染色体的双定向至关重要。在这里,我们已经证明,X 染色体上编码的 RNA 结合基序蛋白(RBMX)通过与染色质而不是 RNA 的关联,在染色体形态发生中发挥着重要作用。通过 RNA 干扰(RNAi)耗尽 RBMX 会导致着丝粒区域在后期之前失去黏合蛋白,导致过早的染色单体分离,并伴有纺锤体检测点蛋白和外层动粒蛋白的去定位。RBMX 耗尽引起的黏合缺陷早在 G2 期就可以检测到。此外,RBMX 与黏合蛋白亚基 Scc1 和 Smc3 以及黏合调节因子 Wapl 相关联。只有在存在 Wapl 的情况下,RBMX 才需要黏合,这表明 RBMX 是 Wapl 的抑制剂。我们提出 RBMX 是一种黏合调节因子,它维持姐妹染色单体的适当黏合。