Teixeira M Teresa, Forstemann Klaus, Gasser Susan M, Lingner Joachim
Swiss Institute for Experimental Cancer Research (ISREC), Epalinges, Switzerland.
EMBO Rep. 2002 Jul;3(7):652-9. doi: 10.1093/embo-reports/kvf133.
Telomerase uses an internal RNA moiety as template for the synthesis of telomere repeats. In Saccharomyces cerevisiae, the telomerase holoenzyme contains the telomerase reverse transcriptase subunit Est2p, the telomerase RNA moiety TLC1, the telomerase associated proteins Est1p and Est3p, and Sm proteins. Here we assess telomerase assembly by determining the localization of telomerase components. We found that Est1p, Est2p and TLC1 can migrate independently of each other to the nucleus. With limiting amounts of TLC1, overexpressed Est1p and Est2p accumulated in the nucleolus, whereas enzymatically active Est2p-TLC1 complexes are distributed over the entire nucleus. The distribution to the nucleoplasm depended on the specific interaction between Est2p and TLC1 but was independent of Est1p and Est3p. Altogether, our results suggest a role of the nucleolus in telomerase biogenesis. We also describe experiments that support a transient cytoplasmic localization of TLC1 RNA.
端粒酶利用其内部的RNA部分作为合成端粒重复序列的模板。在酿酒酵母中,端粒酶全酶包含端粒酶逆转录酶亚基Est2p、端粒酶RNA部分TLC1、端粒酶相关蛋白Est1p和Est3p以及Sm蛋白。在此,我们通过确定端粒酶组分的定位来评估端粒酶组装。我们发现Est1p、Est2p和TLC1能够彼此独立地迁移至细胞核。在TLC1数量有限的情况下,过表达的Est1p和Est2p在核仁中积累,而具有酶活性的Est2p-TLC1复合物则分布于整个细胞核。向核质的分布取决于Est2p与TLC1之间的特异性相互作用,但与Est1p和Est3p无关。总之,我们的结果表明核仁在端粒酶生物合成中发挥作用。我们还描述了支持TLC1 RNA在细胞质中短暂定位的实验。