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Hansenula Polymorpha TERT: A Telomerase Catalytic SubunitIsolated in Recombinant Form with Limited Reverse TranscriptaseActivity

机译:多形汉逊酵母TERT:端粒酶催化亚基。以有限的逆转录酶重组形式分离活动

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摘要

Telomerase is a ribonucleoprotein, the main function of which is to synthesize telomeres, i.e. repetitive sequences which are localized at the ends of eukaryotic chromosomes. Telomerase maintains the stability of the genome in eukaryotic cells by replicating chromosomal ends. The structural and functional investigation of the telomerase complex is significantly restricted due to difficulties connected with the isolation of its main catalytic subunit in recombinant form. Herein, we describe a method developed for the isolation of the recombinant telomerase reverse transcriptase from thermotolerant yeastHansenula polymorpha. A functional test performed for the isolated protein and the RNA/DNA duplex, simulating the interaction of telomerase RNA and telomere, reveals that the isolated catalytic subunit of telomerase possesses limited reverse transcriptase activity.
机译:端粒酶是一种核糖核蛋白,其主要功能是合成端粒,即位于真核染色体末端的重复序列。端粒酶通过复制染色体末端来维持真核细胞中基因组的稳定性。由于端粒酶复合物的主要催化亚基以重组形式的分离存在困难,因此端粒酶复合物的结构和功能研究受到很大限制。在此,我们描述了一种从耐热酵母多形汉逊酵母中分离重组端粒酶逆转录酶的方法。对分离的蛋白质和RNA / DNA双链体进行的功能测试,模拟端粒酶RNA和端粒的相互作用,发现分离的端粒酶催化亚基具有有限的逆转录酶活性。

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