Luo Kunheng, Vega-Palas Miguel A, Grunstein Michael
Department of Biological Chemistry, UCLA School of Medicine, 90095, USA.
Genes Dev. 2002 Jun 15;16(12):1528-39. doi: 10.1101/gad.988802.
In Saccharomyces cerevisiae, heterochromatin-like regions are found near telomeres and at the silent mating-type loci, where they can repress genes in an epigenetic manner. Several proteins are involved in telomeric heterochromatin structure including Rap1, Sir2, Sir3, Sir4, yKu70 (Hdf1), yKu80 (Hdf2), and the N termini of histones H3 and H4. By recognizing cis-acting DNA-binding sites, Rap1 is believed to recruit Sir and other silencing proteins and determine where heterochromatin forms. The integrity of heterochromatin also requires the binding of Sir proteins to histones that may form a scaffold for Sir protein interactions with chromatin. In this study we describe how the heterochromatin complex may form initially and how it differs from the complex that spreads along the chromosome. We found that close to the telomere end, Sir4 can bind Rap1 independently of Sir2, Sir3, yKu70/yKu80, and the intact H4 N terminus. In contrast, Sir4 binding requires all of the silencing factors further along telomeric heterochromatin. These data indicate that Sir4 binding to Rap1 initiates the sequential association of Sir and other proteins, allowing the subsequent spreading of the heterochromatin proteins along the chromosome.
在酿酒酵母中,类似异染色质的区域存在于端粒附近和沉默交配型位点,在这些地方它们可以以表观遗传的方式抑制基因。几种蛋白质参与端粒异染色质结构,包括Rap1、Sir2、Sir3、Sir4、yKu70(Hdf1)、yKu80(Hdf2)以及组蛋白H3和H4的N端。通过识别顺式作用DNA结合位点,Rap1被认为可招募Sir和其他沉默蛋白,并确定异染色质形成的位置。异染色质的完整性还需要Sir蛋白与组蛋白结合,组蛋白可能形成Sir蛋白与染色质相互作用的支架。在本研究中,我们描述了异染色质复合物最初可能如何形成以及它与沿染色体扩散的复合物有何不同。我们发现,靠近端粒末端时,Sir4可以独立于Sir2、Sir3、yKu70/yKu80和完整的H4 N端与Rap1结合。相比之下,在端粒异染色质更远的位置,Sir4的结合需要所有的沉默因子。这些数据表明,Sir4与Rap1的结合启动了Sir和其他蛋白质的顺序结合,使得异染色质蛋白随后能够沿染色体扩散。