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Telomeric G-quadruplexes are a substrate and site of localization for human telomerase

机译:端粒G-四链体是人类端粒酶的底物和定位位点

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It has been hypothesized that G-quadruplexes can sequester the 30 end of the telomere and prevent it from being extended by telomerase. Here we purify and characterize stable, conformationally homogenous human telomeric G-quadruplexes, and demonstrate that human telomerase is able to extend parallel, intermolecular conformations in vitro. These G-quadruplexes align correctly with the RNA template of telomerase, demonstrating that at least partial G-quadruplex resolution is required. A highly purified preparation of human telomerase retains this extension ability, establishing that the core telomerase enzyme complex is sufficient for partial G-quadruplex resolution and extension. The parallel-specific G-quadruplex ligand N-methyl mesoporphyrin IX (NMM) causes an increase in telomeric G-quadruplexes, and we show that telomerase colocalizes with a subset of telomeric G-quadruplexes in vivo. The ability of telomerase to partially unwind, extend and localize to these structures implies that parallel telomeric G-quadruplexes may play an important biological role.
机译:据推测,G-四链体可以隔离端粒的30末端并防止其被端粒酶延伸。在这里,我们纯化和表征稳定,构象同源的人类端粒G四联体,并证明人类端粒酶能够在体外扩展平行,分子间构象。这些G-四链体与端粒酶的RNA模板正确对齐,表明至少需要部分G-四链体分辨率。高纯度的人类端粒酶制剂保留了这种延伸能力,从而确定核心端粒酶复合物足以实现部分G-四链体的分解和延伸。平行特异性G-四链体配体N-甲基中卟啉IX(NMM)导致端粒G-四链体增加,并且我们表明端粒酶在体内与一部分端粒G-四链体共定位。端粒酶部分解旋,延伸和定位于这些结构的能力暗示平行端粒G-四链体可能起重要的生物学作用。

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