Hess David, Liu Bingsheng, Roan Nadia R, Sternglanz Rolf, Winston Fred
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Mol Cell Biol. 2004 Jan;24(1):135-43. doi: 10.1128/MCB.24.1.135-143.2004.
Histone levels are a key factor in several nuclear processes, including transcription and chromosome segregation. Previous studies have demonstrated that Spt10 and Spt21 are required for the normal transcription of a subset of the histone genes in Saccharomyces cerevisiae, and sequence analysis has suggested that Spt10 is an acetyltransferase. We have now characterized several aspects of transcriptional activation of histone genes by Spt10 in vivo. Our results show that activation by Spt10 is dependent on its acetyltransferase domain. At HTA2-HTB2, the histone locus whose transcription is most strongly dependent on Spt10, Spt10 is physically recruited to the promoter in an Spt21-dependent and a cell cycle-dependent manner. Furthermore, Spt10 and Spt21 directly interact. These results, taken together with the identification of spt10 mutations that suppress an spt21Delta mutation, suggest a model for transcriptional activation by Spt10 and Spt21.
组蛋白水平是包括转录和染色体分离在内的多个核过程中的关键因素。先前的研究表明,酿酒酵母中组蛋白基因子集的正常转录需要Spt10和Spt21,并且序列分析表明Spt10是一种乙酰转移酶。我们现在已经在体内对Spt10激活组蛋白基因转录的几个方面进行了表征。我们的结果表明,Spt10的激活依赖于其乙酰转移酶结构域。在HTA2-HTB2(其转录最强烈依赖于Spt10的组蛋白基因座),Spt10以依赖于Spt21和细胞周期的方式被物理募集到启动子。此外,Spt10和Spt21直接相互作用。这些结果,连同抑制spt21Delta突变的spt10突变的鉴定,提出了一个关于Spt10和Spt21转录激活的模型。