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首页> 外文期刊>Nucleic acids research >ATF7 mediates TNF-α–induced telomere shortening
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ATF7 mediates TNF-α–induced telomere shortening

机译:ATF7介导TNF-α诱导的端粒缩短

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摘要

Telomeres maintain the integrity of chromosome ends and telomere length is an important marker of aging. The epidemiological studies suggested that many types of stress including psychosocial stress decrease telomere length. However, it remains unknown how various stresses induce telomere shortening. Here, we report that the stress-responsive transcription factor ATF7 mediates TNF-α–induced telomere shortening. ATF7 and telomerase, an enzyme that elongates telomeres, are localized on telomeres via interactions with the Ku complex. In response to TNF-α, which is induced by various stresses including psychological stress, ATF7 was phosphorylated by p38, leading to the release of ATF7 and telomerase from telomeres. Thus, a decrease of ATF7 and telomerase on telomeres in response to stress causes telomere shortening, as observed in ATF7-deficient mice. These findings give credence to the idea that various types of stress might shorten telomere.
机译:端粒保持染色体末端的完整性,端粒长度是衰​​老的重要标志。流行病学研究表明,包括心理社会压力在内的许多类型的压力都会降低端粒的长度。但是,仍然不清楚各种压力如何导致端粒缩短。在这里,我们报道应激反应转录因子ATF7介导TNF-α诱导的端粒缩短。 ATF7和端粒酶(一种延长端粒的酶)通过与Ku配合物的相互作用而定位在端粒上。响应由各种压力(包括心理压力)诱导的TNF-α,ATF7被p38磷酸化,导致ATF7和端粒酶从端粒释放。因此,如在ATF7缺陷型小鼠中观察到的那样,响应压力,端粒上ATF7和端粒酶的减少会导致端粒缩短。这些发现证实了各种压力可能会缩短端粒的观点。

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