Kishi Shuji, Lu Kun Ping
Cancer Biology Program, Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.
J Biol Chem. 2002 Mar 1;277(9):7420-9. doi: 10.1074/jbc.M111365200. Epub 2001 Dec 13.
Cells derived from patients with the human genetic disorder ataxia-telangiectasia (A-T) display many abnormalities, including telomere shortening, premature senescence, and defects in the activation of S phase and G(2)/M checkpoints in response to double-strand DNA breaks induced by ionizing radiation. We have previously demonstrated that one of the ATM substrates is Pin2/TRF1, a telomeric protein that binds the potent telomerase inhibitor PinX1, negatively regulates telomere elongation, and specifically affects mitotic progression. Following DNA damage, ATM phosphorylates Pin2/TRF1 and suppresses its ability to induce abortive mitosis and apoptosis (Kishi, S., Zhou, X. Z., Nakamura, N., Ziv, Y., Khoo, C., Hill, D. E., Shiloh, Y., and Lu, K. P. (2001) J. Biol. Chem. 276, 29282-29291). However, the functional importance of Pin2/TRF1 in mediating ATM-dependent regulation remains to be established. To address this question, we directly inhibited the function of endogenous Pin2/TRF1 in A-T cells by stable expression of two different dominant-negative Pin2/TRF1 mutants and then examined their effects on telomere length and DNA damage response. Both the Pin2/TRF1 mutants increased telomere length in A-T cells, as shown in other cells. Surprisingly, both the Pin2/TRF1 mutants reduced radiosensitivity and complemented the G(2)/M checkpoint defect without inhibiting Cdc2 activity in A-T cells. In contrast, neither of the Pin2/TRF1 mutants corrected the S phase checkpoint defect in the same cells. These results indicate that inhibition of Pin2/TRF1 in A-T cells is able to bypass the requirement for ATM in specifically restoring telomere shortening, the G(2)/M checkpoint defect, and radiosensitivity and demonstrate a critical role for Pin2/TRF1 in the ATM-dependent regulation of telomeres and DNA damage response.
源自患有人类遗传性共济失调毛细血管扩张症(A-T)患者的细胞表现出许多异常,包括端粒缩短、过早衰老以及在响应电离辐射诱导的双链DNA断裂时S期和G(2)/M期检查点激活缺陷。我们先前已证明,ATM的底物之一是Pin2/TRF1,一种端粒蛋白,它结合有效的端粒酶抑制剂PinX1,负向调节端粒延长,并特别影响有丝分裂进程。DNA损伤后,ATM使Pin2/TRF1磷酸化并抑制其诱导流产性有丝分裂和凋亡的能力(岸本,S.,周,X.Z.,中村,N.,齐夫,Y.,邱,C.,希尔,D.E.,希洛,Y.,和卢,K.P.(2001年)《生物化学杂志》276,29282 - 29291)。然而,Pin2/TRF1在介导ATM依赖性调节中的功能重要性仍有待确定。为了解决这个问题,我们通过稳定表达两种不同的显性负性Pin2/TRF1突变体直接抑制A-T细胞中内源性Pin2/TRF1的功能,然后检查它们对端粒长度和DNA损伤反应的影响。如在其他细胞中所示,两种Pin2/TRF1突变体均增加了A-T细胞中的端粒长度。令人惊讶的是,两种Pin2/TRF1突变体均降低了放射敏感性并弥补了G(2)/M期检查点缺陷,而未抑制A-T细胞中的Cdc2活性。相反,两种Pin2/TRF1突变体均未纠正同一细胞中的S期检查点缺陷。这些结果表明,在A-T细胞中抑制Pin2/TRF1能够在特异性恢复端粒缩短、G(2)/M期检查点缺陷和放射敏感性方面绕过对ATM的需求,并证明Pin2/TRF1在ATM依赖性端粒调节和DNA损伤反应中起关键作用。