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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Telomerase repeat addition processivity is increased at critically short telomeres in a Tel1-dependent manner in Saccharomyces cerevisiae.
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Telomerase repeat addition processivity is increased at critically short telomeres in a Tel1-dependent manner in Saccharomyces cerevisiae.

机译:在酿酒酵母中,以Tel1依赖的方式在临界短端粒上增加端粒酶重复添加的持续性。

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摘要

Telomerase is the ribonucleoprotein enzyme that elongates telomeres to counteract telomere shortening. The core enzyme consists of a reverse transcriptase protein subunit and an RNA subunit. The RNA subunit contains a short region that is used as a template by the reverse transcriptase to add short, tandem, G-rich repeats to the 3' ends of telomeres. By coexpressing two RNA subunits that differ in the telomeric repeat sequence specified and examining the telomere extensions after one cell cycle, we determined that Saccharomyces cerevisiae telomerase can dissociate and reassociate from a given telomere during one cell cycle. We also confirmed that telomerase is nonprocessive in terms of telomeric repeat addition. However, repeat addition processivity is significantly increased at extremely short telomeres, a process that is dependent on the ATM-ortholog Tel1. We propose that this enhancement of telomerase processivity at short telomeres serves to rapidly elongate critically short telomeres.
机译:端粒酶是延长端粒以抵消端粒缩短的核糖核蛋白酶。核心酶由逆转录酶蛋白亚基和RNA亚基组成。 RNA亚基包含一个短区域,该短区域被逆转录酶用作模板,以向端粒的3'末端添加短的,串联的,富含G的重复序列。通过共表达两个指定的端粒重复序列不同的RNA亚基并在一个细胞周期后检查端粒的延伸,我们确定了酿酒酵母端粒酶可以在一个细胞周期内与给定的端粒解离并重新结合。我们还证实,就端粒重复添加而言,端粒酶是非加工性的。但是,在极短的端粒中重复添加的合成能力显着提高,该过程取决于ATM-直向同源物Tel1。我们建议在端粒短时增强端粒酶的合成能力可迅速延长临界短端粒。

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