Roberts S M, Winston F
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genetics. 1997 Oct;147(2):451-65. doi: 10.1093/genetics/147.2.451.
The Saccharomyces cerevisiae transcription factor Spt20/Ada5 was originally identified by mutations that suppress Ty insertion alleles and by mutations that suppress the toxicity caused by Gal4-VP16 overexpression. Here we present evidence for physical associations between Spt20/Ada5 and three other Spt proteins, suggesting that they exist in a complex. A related study demonstrates that this complex also contains the histone acetyltransferase, Gcn5, and Ada2. This complex has been named SAGA (Spt/Ada/Gcn5 acetyltransferase). To identify functions that genetically interact with SAGA, we have screened for mutations that cause lethality in an spt20 delta/ada5 delta mutant. Our screen identified mutations in SNF2, SIN4, and GAL11. These mutations affect two known transcription complexes: Snf/Swi, which functions in nucleosome remodeling, and Srb/mediator, which is required for regulated transcription by RNA polymerase II. Systematic analysis has demonstrated that spt20 delta/ada5 delta and spt7 delta mutations cause lethality with every snf/swi and srb/mediator mutation tested. Furthermore, a gcn5 delta mutation causes severe sickness with snf/swi mutations, but not with srb/mediator mutations. These findings suggest that SAGA has multiple activities and plays critical roles in transcription by RNA polymerase II.
酿酒酵母转录因子Spt20/Ada5最初是通过抑制Ty插入等位基因的突变以及抑制Gal4-VP16过表达所导致毒性的突变而被鉴定出来的。在此,我们提供证据表明Spt20/Ada5与其他三种Spt蛋白之间存在物理关联,这表明它们以复合物形式存在。一项相关研究表明,该复合物还包含组蛋白乙酰转移酶Gcn5和Ada2。这个复合物被命名为SAGA(Spt/Ada/Gcn5乙酰转移酶)。为了鉴定与SAGA发生遗传相互作用的功能,我们筛选了在spt20Δ/ada5Δ突变体中导致致死性的突变。我们的筛选鉴定出了SNF2、SIN4和GAL11中的突变。这些突变影响两种已知的转录复合物:在核小体重塑中起作用的Snf/Swi,以及RNA聚合酶II进行调控转录所必需的Srb/中介体。系统分析表明,spt20Δ/ada5Δ和spt7Δ突变与所测试的每一个snf/swi和srb/中介体突变都会导致致死性。此外,gcn5Δ突变与snf/swi突变一起会导致严重病变,但与srb/中介体突变一起则不会。这些发现表明SAGA具有多种活性,并在RNA聚合酶II的转录过程中发挥关键作用。