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裂殖酵母泛素缀合酶UbcP3、Ubc15和Rhp6影响交配型区域的转录沉默。

The fission yeast ubiquitin-conjugating enzymes UbcP3, Ubc15, and Rhp6 affect transcriptional silencing of the mating-type region.

作者信息

Nielsen Inga Sig, Nielsen Olaf, Murray Johanne M, Thon Geneviève

机构信息

Department of Genetics, Institute of Molecular Biology, University of Copenhagen, DK-1353 Copenhagen K, Denmark.

出版信息

Eukaryot Cell. 2002 Aug;1(4):613-25. doi: 10.1128/EC.1.4.613-625.2002.

Abstract

Genes transcribed by RNA polymerase II are silenced when introduced near the mat2 or mat3 mating-type loci of the fission yeast Schizosaccharomyces pombe. Silencing is mediated by a number of gene products and cis-acting elements. We report here the finding of novel trans-acting factors identified in a screen for high-copy-number disruptors of silencing. Expression of cDNAs encoding the putative E2 ubiquitin-conjugating enzymes UbcP3, Ubc15 (ubiquitin-conjugating enzyme), or Rhp6 (Rad homolog pombe) from the strong nmt1 promoter derepressed the silent mating-type loci mat2 and mat3 and reporter genes inserted nearby. Deletion of rhp6 slightly derepressed an ade6 reporter gene placed in the mating-type region, whereas disruption of ubcP3 or ubc15 had no obvious effect on silencing. Rhp18 is the S. pombe homolog of Saccharomyces cerevisiae Rad18p, a DNA-binding protein that physically interacts with Rad6p. Rhp18 was not required for the derepression observed when UbcP3, Ubc15, or Rhp6 was overproduced. Overexpressing Rhp6 active-site mutants showed that the ubiquitin-conjugating activity of Rhp6 is essential for disruption of silencing. However, high dosage of UbcP3, Ubc15, or Rhp6 was not suppressed by a mutation in the 26S proteasome, suggesting that loss of silencing is not due to an increased degradation of silencing factors but rather to the posttranslational modification of proteins by ubiquitination. We discuss the implications of these results for the possible modes of action of UbcP3, Ubc15, and Rhp6.

摘要

当RNA聚合酶II转录的基因被导入到裂殖酵母粟酒裂殖酵母的mat2或mat3交配型位点附近时,这些基因会被沉默。沉默是由多种基因产物和顺式作用元件介导的。我们在此报告在筛选沉默的高拷贝数破坏因子的过程中发现的新型反式作用因子。从强nmt1启动子表达编码假定的E2泛素缀合酶UbcP3、Ubc15(泛素缀合酶)或Rhp6(粟酒裂殖酵母Rad同源物)的cDNA,可解除沉默的交配型位点mat2和mat3以及附近插入的报告基因的抑制。缺失rhp6会轻微解除位于交配型区域的ade6报告基因的抑制,而破坏ubcP3或ubc15对沉默没有明显影响。Rhp18是酿酒酵母Rad18p的粟酒裂殖酵母同源物,Rad18p是一种与Rad6p发生物理相互作用的DNA结合蛋白。当过量表达UbcP3、Ubc15或Rhp6时,观察到的去抑制作用不需要Rhp18。过表达Rhp6活性位点突变体表明,Rhp6的泛素缀合活性对于破坏沉默至关重要。然而,26S蛋白酶体中的突变并没有抑制高剂量的UbcP3、Ubc15或Rhp6,这表明沉默丧失不是由于沉默因子降解增加,而是由于蛋白质通过泛素化进行的翻译后修饰。我们讨论了这些结果对UbcP3、Ubc15和Rhp6可能作用模式的影响。

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