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端粒蛋白TRF2与ATM激酶结合,并能抑制ATM依赖的DNA损伤反应。

The telomeric protein TRF2 binds the ATM kinase and can inhibit the ATM-dependent DNA damage response.

作者信息

Karlseder Jan, Hoke Kristina, Mirzoeva Olga K, Bakkenist Christopher, Kastan Michael B, Petrini John H J, de Lange Titia

机构信息

Laboratory for Cell Biology and Genetics, Rockefeller University, New York, USA.

出版信息

PLoS Biol. 2004 Aug;2(8):E240. doi: 10.1371/journal.pbio.0020240. Epub 2004 Aug 17.

Abstract

The telomeric protein TRF2 is required to prevent mammalian telomeres from activating DNA damage checkpoints. Here we show that overexpression of TRF2 affects the response of the ATM kinase to DNA damage. Overexpression of TRF2 abrogated the cell cycle arrest after ionizing radiation and diminished several other readouts of the DNA damage response, including phosphorylation of Nbs1, induction of p53, and upregulation of p53 targets. TRF2 inhibited autophosphorylation of ATM on S1981, an early step in the activation of this kinase. A region of ATM containing S1981 was found to directly interact with TRF2 in vitro, and ATM immunoprecipitates contained TRF2. We propose that TRF2 has the ability to inhibit ATM activation at telomeres. Because TRF2 is abundant at chromosome ends but not elsewhere in the nucleus, this mechanism of checkpoint control could specifically block a DNA damage response at telomeres without affecting the surveillance of chromosome internal damage.

摘要

端粒蛋白TRF2是防止哺乳动物端粒激活DNA损伤检查点所必需的。在此我们表明,TRF2的过表达会影响ATM激酶对DNA损伤的反应。TRF2的过表达消除了电离辐射后的细胞周期停滞,并减少了DNA损伤反应的其他几个指标,包括Nbs1的磷酸化、p53的诱导以及p53靶标的上调。TRF2抑制了ATM在S1981位点的自身磷酸化,这是该激酶激活的早期步骤。发现含有S1981的ATM区域在体外可与TRF2直接相互作用,并且ATM免疫沉淀复合物中含有TRF2。我们提出,TRF2具有在端粒处抑制ATM激活的能力。由于TRF2在染色体末端丰富而在细胞核的其他位置不存在,这种检查点控制机制可以特异性地阻断端粒处的DNA损伤反应,而不影响对染色体内部损伤的监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a586/509302/a546fee1ca34/pbio.0020240.g001.jpg

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