Enomoto S, Johnston S D, Berman J
Department of Genetics, Cell Biology and Development, University of Minnesota, St. Paul 55108, USA.
Genetics. 2000 Jun;155(2):523-38. doi: 10.1093/genetics/155.2.523.
Using a screen for genes that affect telomere function, we isolated sir3-P898R, an allele of SIR3 that reduces telomeric silencing yet does not affect mating. While sir3-P898R mutations cause no detectable mating defect in quantitative assays, they result in synergistic mating defects in combination with mutations such as sir1 that affect the establishment of silencing. In contrast, sir3-P898R in combination with a cac1 mutation, which affects the maintenance of silencing, does not result in synergistic mating defects. MATa sir3-P898R mutants form shmoo clusters in response to alpha-factor, and sir3-P898R strains are capable of establishing silencing at a previously derepressed HML locus with kinetics like that of wild-type SIR3 strains. These results imply that Sir3-P898Rp is defective in the maintenance, but not the establishment of silencing. In addition, overexpression of a C-terminal fragment of Sir3-P898R results in a dominant nonmating phenotype: HM silencing is completely lost at both HML and HMR. Furthermore, HM silencing is most vulnerable to disruption by the Sir3-P898R C terminus immediately after S-phase, the time when new silent chromatin is assembled onto newly replicated DNA.
通过筛选影响端粒功能的基因,我们分离出了sir3-P898R,它是SIR3的一个等位基因,可降低端粒沉默但不影响交配。虽然在定量分析中,sir3-P898R突变未导致可检测到的交配缺陷,但与影响沉默建立的突变(如sir1)相结合时,它们会导致协同交配缺陷。相比之下,sir3-P898R与影响沉默维持的cac1突变相结合,不会导致协同交配缺陷。MATa sir3-P898R突变体在α-因子作用下形成了芽管簇,并且sir3-P898R菌株能够在先前去抑制的HML位点建立沉默,其动力学与野生型SIR3菌株相似。这些结果表明,Sir3-P898Rp在沉默维持方面存在缺陷,但在沉默建立方面没有缺陷。此外,Sir3-P898R C末端片段的过表达导致显性不交配表型:HML和HMR处的HM沉默完全丧失。此外,在S期之后,即新的沉默染色质组装到新复制的DNA上的时间,HM沉默最容易受到Sir3-P898R C末端的破坏。