McCord Ron, Pierce Michael, Xie Jianxin, Wonkatal Sandeep, Mickel Carolyn, Vershon Andrew K
Waksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, 190 Frelinghuysen Road, Piscataway, NJ 08854, USA.
Mol Cell Biol. 2003 Mar;23(6):2009-16. doi: 10.1128/MCB.23.6.2009-2016.2003.
Transcriptional repression is often correlated with the alteration of chromatin structure through modifications of the nucleosomes in the promoter region, such as by deacetylation of the N-terminal histone tails. This is presumed to make the promoter region inaccessible to other regulatory factors and the general transcription machinery. To accomplish this, histone deacetylases are recruited to specific promoters via DNA-binding proteins and tethering factors. We have previously reported the requirement for the NAD(+)-dependent histone deacetylase Hst1 and the DNA-binding protein Sum1 for vegetative repression of many middle sporulation genes in Saccharomyces cerevisiae. Here we report the identification of a novel tethering factor, Rfm1, that is required for Hst1-mediated repression. Rfm1 interacts with both Sum1 and Hst1 and is required for the Sum1-Hst1 interaction. DNA microarray and Northern blot analyses showed that Rfm1 is required for repression of the same subset of Sum1-repressed genes that require Hst1. These results suggest that Rfm1 is a specificity factor that targets the Hst1 deacetylase to a subset of Sum1-regulated genes.
转录抑制通常与启动子区域核小体修饰引起的染色质结构改变相关,例如通过N端组蛋白尾巴的去乙酰化。据推测,这会使启动子区域对其他调节因子和通用转录机制不可接近。为实现这一点,组蛋白去乙酰化酶通过DNA结合蛋白和拴系因子被招募到特定启动子。我们之前报道过,酿酒酵母中许多中期孢子形成基因的营养生长抑制需要NAD(+)依赖性组蛋白去乙酰化酶Hst1和DNA结合蛋白Sum1。在此我们报道了一种新型拴系因子Rfm1的鉴定,它是Hst1介导的抑制所必需的。Rfm1与Sum1和Hst1都相互作用,并且是Sum1-Hst1相互作用所必需的。DNA微阵列和Northern印迹分析表明,Rfm1是抑制需要Hst1的Sum1抑制基因的同一子集所必需的。这些结果表明,Rfm1是一种特异性因子,它将Hst1去乙酰化酶靶向Sum1调节基因的一个子集。