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Humanized telomeres and an attempt to express a functional human telomerase in yeast

机译:人源化端粒和在酵母中表达功能性人端粒酶的尝试

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摘要

The maintenance of telomeric repeat DNA depends on an evolutionarily conserved reverse trans criptase called telomerase. In vitro, only the catalytic subunit and a telomerase-associated RNA are required for the synthesis of species-specific repeat DNA. In an attempt to establish a heterologous system for the study of the human telomerase enzyme, we expressed the two core components and predicted regulatory subunits in the yeast Saccharomyces cerevisiae. We show that adequate substrates for human telomerase can be generated; the expressed enzyme was localized in the nucleus and it had the capacity to synthesize human-specific repeats in vitro. However, there was no evidence for human telomerase activity at yeast telomeres in vivo. Therefore functional replacement of the yeast telomerase by the human enzyme may require additional human-specific components. We also replaced the template region of the yeast telomerase RNA with one that dictates the synthesis of vertebrate repeats and performed a detailed molecular analysis of the composition of the telomeres upon outgrowth of such strains. The results suggest that vertebrate repeats on yeast telomeres are subject to a very high degree of repeat turnover and show that an innermost tract of 50 bp of yeast repeats are resistant to replacement.
机译:端粒重复DNA的维持取决于进化上保守的逆转录酶,即端粒酶。在体外,仅催化亚基和端粒酶相关的RNA即可合成物种特异性重复DNA。为了建立一个用于研究人类端粒酶的异源系统,我们在酿酒酵母中表达了两个核心成分并预测了调控亚基。我们表明可以产生足够的底物,用于人类端粒酶。表达的酶位于细胞核中,并具有在体外合成人特异性重复序列的能力。然而,没有证据表明人体内酵母端粒具有人类端粒酶活性。因此,人端酶对酵母端粒酶的功能替代可能需要其他人特异性成分。我们还用指示脊椎动物重复序列合成的酵母端粒酶RNA的模板区域替换了模板,并在此类菌株长大后对端粒的组成进行了详细的分子分析。结果表明,酵母端粒上的脊椎动物重复序列具有很高的重复序列重复率,并且表明酵母重复序列的最内层50 bp对置换具有抗性。

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