Jády Beáta E, Richard Patricia, Bertrand Edouard, Kiss Tamás
Laboratoire de Biologie Moléculaire Eucaryote du CNRS, UMR5099, IFR109, 31062 Toulouse, France.
Mol Biol Cell. 2006 Feb;17(2):944-54. doi: 10.1091/mbc.e05-09-0904. Epub 2005 Nov 30.
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.
端粒酶是一种核糖核蛋白酶,通过在染色体末端添加端粒序列重复片段来对抗复制性端粒侵蚀。尽管端粒酶在端粒合成中的作用已得到充分证实,但尚未在端粒处检测到它。人端粒酶的RNA成分(hTR)存在于间期癌细胞的核质卡哈尔体(CBs)中。在此,原位杂交表明,在人HeLa和Hep2 S期细胞中,除了在CBs中积累外,hTR还特异性地集中在一些端粒上,这些端粒也积累了TRF1和TRF2端粒标记蛋白。令人惊讶的是,积累hTR的端粒在不进行染色质变性的情况下对原位寡核苷酸杂交具有很高的可及性,这表明它们代表了HeLa端粒中结构上不同的一小部分。此外,我们证明超过25%积累hTR的端粒与CBs共定位。延时荧光显微镜显示,在S期细胞核质中移动的CBs与端粒短暂结合10 - 40分钟。我们的数据提出了一个有趣的可能性,即CBs可能将hTR递送至端粒和/或可能在端粒维持的其他方面发挥作用。