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首页> 外文期刊>Molecular biology of the cell >An InCytes from MBC Selection: CENP-H–containing Complex Facilitates Centromere Deposition of CENP-A in Cooperation with FACT and CHD1
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An InCytes from MBC Selection: CENP-H–containing Complex Facilitates Centromere Deposition of CENP-A in Cooperation with FACT and CHD1

机译:从MBC选择中获得的InCytes:与FACT和CHD1合作,含有CENP-H的复合物促进CENP-A的着丝粒沉积

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摘要

Centromere identity is thought to be determined by epigenetic mechanisms. The centromere-specific histone H3 variant CENP-A plays a central role in specifying the locus where the centromere is constructed. However, the precise mechanisms that target CENP-A to centromeric chromatin are poorly understood. Here, we show that facilitates chromatin transcription (FACT) localizes to centromeres in a CENP-H–containing complex-dependent manner. In conditional mutant cell lines for SSRP1, a subunit of FACT, centromere targeting of newly synthesized CENP-A is severely inhibited. The chromatin remodeling factor CHD1 binds to SSRP1 both in vivo and in vitro and associates with centromeres. The centromeric localization of CHD1 is lost in SSRP1-depleted cells. RNA interference knockdown of CHD1 leads to a decrease in the amount of centromere localized CENP-A. These findings indicate that the CENP-H–containing complex facilitates deposition of newly synthesized CENP-A into centromeric chromatin in cooperation with FACT and CHD1.
机译:着丝粒身份被认为是由表观遗传机制决定的。着丝粒特异的组蛋白H3变异体CENP-A在确定着丝粒所在的基因座中起着核心作用。但是,将CENP-A靶向着丝粒染色质的精确机制了解甚少。在这里,我们显示了促进染色质转录(FACT)以CENP-H包含的复合物依赖性方式定位于着丝粒。在FACT的亚基SSRP1的条件突变细胞系中,新合成的CENP-A的着丝粒靶向受到严重抑制。染色质重塑因子CHD1在体内和体外均与SSRP1结合,并与着丝粒相关。 CHD1的着丝粒定位在SSRP1耗尽的细胞中丢失。 CHD1的RNA干扰敲低导致着丝粒定位的CENP-A数量减少。这些发现表明,与FACT和CHD1合作,含CENP-H的复合物可促进新合成的CENP-A沉积到着丝粒染色质中。

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