Hsiao Susan J, Poitras Marc F, Cook Brandoch D, Liu Yie, Smith Susan
Skirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Avenue, 2nd Floor, New York, NY 10016, USA.
Mol Cell Biol. 2006 Mar;26(6):2044-54. doi: 10.1128/MCB.26.6.2044-2054.2006.
Regulation of telomere length maintenance and capping are a critical cell functions in both normal and tumor cells. Tankyrase 2 (Tnks2) is a poly(ADP-ribose) polymerase (PARP) that has been shown to modify itself and TRF1, a telomere-binding protein. We show here by overexpression studies that tankyrase 2, like its closely related homolog tankyrase 1, can function as a positive regulator of telomere length in human cells, dependent on its catalytic PARP activity. To study the role of Tnks2 in vivo, we generated mice with the Tnks2 PARP domain deleted. These mice are viable and fertile but display a growth retardation phenotype. Telomere analysis by quantitative fluorescence in situ hybridization (FISH), flow-FISH, and restriction fragment analysis showed no change in telomere length or telomere capping in these mice. To determine the requirement for Tnks2 in long-term maintenance of telomeres, we generated embryonic stem cells with the Tnks2 PARP domain deleted and observed no change, even upon prolonged growth, in telomere length or telomere capping. Together, these results suggest that Tnks2 has a role in normal growth and development but is not essential for telomere length maintenance or telomere capping in mice.
端粒长度维持和封端的调控是正常细胞和肿瘤细胞中的关键细胞功能。端锚聚合酶2(Tnks2)是一种聚(ADP-核糖)聚合酶(PARP),已被证明可对自身及端粒结合蛋白TRF1进行修饰。我们通过过表达研究表明,端锚聚合酶2与其密切相关的同源物端锚聚合酶1一样,可作为人类细胞中端粒长度的正向调节因子,这依赖于其催化性PARP活性。为了研究Tnks2在体内的作用,我们构建了缺失Tnks2 PARP结构域的小鼠。这些小鼠可存活且可育,但表现出生长迟缓的表型。通过定量荧光原位杂交(FISH)、流式FISH和限制性片段分析进行的端粒分析表明,这些小鼠的端粒长度或端粒封端没有变化。为了确定Tnks2在端粒长期维持中的需求,我们构建了缺失Tnks2 PARP结构域的胚胎干细胞,并且观察到即使在长期生长后,端粒长度或端粒封端也没有变化。总之,这些结果表明,Tnks2在正常生长和发育中起作用,但对小鼠的端粒长度维持或端粒封端并非必不可少。