Lendvay T S, Morris D K, Sah J, Balasubramanian B, Lundblad V
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
Genetics. 1996 Dec;144(4):1399-412. doi: 10.1093/genetics/144.4.1399.
The primary determinant for telomere replication is the enzyme telomerase, responsible for elongating the G-rich strand of the telomere. The only component of this enzyme that has been identified in Saccharomyces cerevisiae is the TLC1 gene, encoding the telomerase RNA subunit. However, a yeast strain defective for the EST1 gene exhibits the same phenotypes (progressively shorter telomeres and a senescence phenotype) as a strain deleted for TLC1, suggesting that EST1 encodes either a component of telomerase or some other factor essential for telomerase function. We designed a multitiered screen that led to the isolation of 22 mutants that display the same phenotypes as est1 and tlc1 mutant strains. These mutations mapped to four complementation groups: the previously identified EST1 gene and three additional genes, called EST2, EST3 and EST4. Cloning of the EST2 gene demonstrated that it encodes a large, extremely basic novel protein with no motifs that provide clues as to function. Epistasis analysis indicated that the four EST genes function in the same pathway for telomere replication as defined by the TLC1 gene, suggesting that the EST genes encode either components of telomerase or factors that positively regulate telomerase activity.
端粒复制的主要决定因素是端粒酶,它负责延长端粒富含G的链。在酿酒酵母中已鉴定出的该酶的唯一成分是TLC1基因,它编码端粒酶RNA亚基。然而,一个EST1基因缺陷的酵母菌株表现出与TLC1缺失菌株相同的表型(端粒逐渐缩短和衰老表型),这表明EST1要么编码端粒酶的一个成分,要么编码对端粒酶功能至关重要的其他某种因子。我们设计了一个多层筛选方法,分离出了22个与est1和tlc1突变菌株表现出相同表型的突变体。这些突变定位于四个互补群:先前鉴定出的EST1基因以及另外三个基因,分别称为EST2、EST3和EST4。EST2基因的克隆表明,它编码一种大型的、碱性极强的新型蛋白质,没有任何能提供功能线索的基序。上位性分析表明,这四个EST基因在由TLC1基因定义的端粒复制同一途径中发挥作用,这表明EST基因要么编码端粒酶的成分,要么编码正向调节端粒酶活性的因子。