Kamakaka R T, Rine J
Division of Genetics, Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.
Genetics. 1998 Jun;149(2):903-14. doi: 10.1093/genetics/149.2.903.
A promoter fusion library of Saccharomyces cerevisiae genes was used to exploit phenotypes associated with altered protein dosage. We identified a novel gene, SAS10, by the ability of Sas10p, when overproduced, to disrupt silencing. The predicted Sas10p was 70,200 kD and strikingly rich in charged amino acids. Sas10p was exclusively nuclear in all stages of the cell cycle. Overproduction of Sas10p caused derepression of mating type genes at both HML and HMR, as well as of URA3, TRP1, and ADE2 when inserted near a telomere or at HMR or the rDNA locus. Repressed genes not associated with silenced chromatin were unaffected. Sas10p was essential for viability, and the termination point following Sas10p depletion was as large budded cells. Remarkably, Sas10p overproduction disrupted silencing even under conditions that bypassed the requirement for Sir proteins, ORC, and Rap1p in silencing. These data implied that Sas10p function was intimately connected with the structure of silenced chromatin.
利用酿酒酵母基因的启动子融合文库来研究与蛋白质剂量改变相关的表型。我们通过过量表达时Sas10p破坏沉默的能力鉴定出一个新基因SAS10。预测的Sas10p为70200 kD,且富含带电荷的氨基酸。在细胞周期的所有阶段,Sas10p都仅存在于细胞核中。Sas10p的过量表达导致HML和HMR处的交配型基因以及插入端粒附近、HMR或rDNA位点时的URA3、TRP1和ADE2基因去抑制。与沉默染色质无关的受抑制基因不受影响。Sas10p对细胞活力至关重要,Sas10p耗尽后的终止点是大芽殖细胞。值得注意的是,即使在绕过沉默中对Sir蛋白、ORC和Rap1p的需求的条件下,Sas10p的过量表达也会破坏沉默。这些数据表明Sas10p的功能与沉默染色质的结构密切相关。