Kogut Igor, Wang Jianbin, Guacci Vincent, Mistry Rohinton K, Megee Paul C
Department of Biochemistry and Molecular Genetics, University of Colorado Denver School of Medicine, Aurora, Colorado 80045, USA.
Genes Dev. 2009 Oct 1;23(19):2345-57. doi: 10.1101/gad.1819409.
Cohesins mediate sister chromatid cohesion and DNA repair and also function in gene regulation. Chromosomal cohesins are distributed nonrandomly, and their deposition requires the heterodimeric Scc2/Scc4 loader. Whether Scc2/Scc4 establishes nonrandom cohesin distributions on chromosomes is poorly characterized, however. To better understand the spatial regulation of cohesin association, we mapped budding yeast Scc2 and Scc4 chromosomal distributions. We find that Scc2/Scc4 resides at previously mapped cohesin-associated regions (CARs) in pericentromeric and arm regions, and that Scc2/Scc4-cohesin colocalization persists after the initial deposition of cohesins in G1/S phase. Pericentromeric Scc2/Scc4 enrichment is kinetochore-dependent, and both Scc2/Scc4 and cohesin associations are coordinately reduced in these regions following chromosome biorientation. Thus, these characteristics of Scc2/Scc4 binding closely recapitulate those of cohesin. Although present in G1, Scc2/Scc4 initially has a poor affinity for CARs, but its affinity increases as cells traverse the cell cycle. Scc2/Scc4 association with CARs is independent of cohesin, however. Taken together, these observations are inconsistent with a previous suggestion that cohesins are relocated by translocating RNA polymerases from separate loading sites to intergenic regions between convergently transcribed genes. Rather, our findings suggest that budding yeast cohesins are targeted to CARs largely by Scc2/Scc4 loader association at these locations.
黏连蛋白介导姐妹染色单体黏连和DNA修复,并且在基因调控中也发挥作用。染色体黏连蛋白呈非随机分布,其沉积需要异二聚体Scc2/Scc4装载蛋白。然而,Scc2/Scc4是否在染色体上建立非随机的黏连蛋白分布还不清楚。为了更好地理解黏连蛋白结合的空间调控,我们绘制了芽殖酵母Scc2和Scc4的染色体分布图谱。我们发现Scc2/Scc4位于着丝粒周围和臂区域中先前定位的黏连蛋白相关区域(CARs),并且在G1/S期黏连蛋白初始沉积后,Scc2/Scc4-黏连蛋白共定位持续存在。着丝粒周围Scc2/Scc4的富集依赖于动粒,并且在染色体双定向后,这些区域中Scc2/Scc4和黏连蛋白的结合都协同减少。因此,Scc2/Scc4结合的这些特征与黏连蛋白的特征密切相似。尽管Scc2/Scc4在G1期存在,但其最初对CARs的亲和力较差,但随着细胞穿越细胞周期,其亲和力会增加。然而,Scc2/Scc4与CARs的结合独立于黏连蛋白。综上所述,这些观察结果与之前的一种观点不一致,该观点认为黏连蛋白通过将RNA聚合酶从单独的装载位点转移到同向转录基因之间的基因间区域而重新定位。相反,我们的研究结果表明,芽殖酵母黏连蛋白主要通过Scc2/Scc4装载蛋白在这些位置的结合而靶向CARs。