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Cell cycle-dependent recruitment of telomerase RNA and Cajal bodies to human telomeres.

机译:端粒酶RNA和Cajal体向人端粒的细胞周期依赖性募集。

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摘要

Telomerase is a ribonucleoprotein enzyme that counteracts replicative telomere erosion by adding telomeric sequence repeats onto chromosome ends. Despite its well-established role in telomere synthesis, telomerase has not yet been detected at telomeres. The RNA component of human telomerase (hTR) resides in the nucleoplasmic Cajal bodies (CBs) of interphase cancer cells. Here, in situ hybridization demonstrates that in human HeLa and Hep2 S phase cells, besides accumulating in CBs, hTR specifically concentrates at a few telomeres that also accumulate the TRF1 and TRF2 telomere marker proteins. Surprisingly, telomeres accumulating hTR exhibit a great accessibility for in situ oligonucleotide hybridization without chromatin denaturation, suggesting that they represent a structurally distinct, minor subset of HeLa telomeres. Moreover, we demonstrate that more than 25% of telomeres accumulating hTR colocalize with CBs. Time-lapse fluorescence microscopy demonstrates that CBs moving in the nucleoplasm of S phase cells transiently associate for 10-40 min with telomeres. Our data raise the intriguing possibility that CBs may deliver hTR to telomeres and/or may function in other aspects of telomere maintenance.
机译:端粒酶是一种核糖核酸蛋白酶,可通过在染色体末端添加端粒序列重复来抵消端粒的复制。尽管其在端粒合成中已确立的作用,但尚未在端粒中检测到端粒酶。人类端粒酶(hTR)的RNA成分位于相间癌细胞的核质Cajal体(CBs)中。在这里,原位杂交表明,在人类HeLa和Hep2 S期细胞中,hTR除了在CB中积累外,还专门集中在几个端粒上,这些端粒也积累了TRF1和TRF2端粒标记蛋白。出乎意料的是,积累了hTR的端粒在不染色质变性的情况下对原位寡核苷酸杂交显示出极大的可及性,这表明它们代表了HeLa端粒的结构独特的次要亚型。此外,我们证明了积累hTR的端粒中有超过25%与CBs共定位。延时荧光显微镜显示,在S期细胞核质中移动的CB与端粒短暂缔合10-40分钟。我们的数据提出了有趣的可能性,即CB可能将hTR传递至端粒和/或可能在端粒维持的其他方面起作用。

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