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ATF7 mediates TNF-alpha-induced telomere shortening

机译:ATF7介质TNF-α诱导的端粒缩短

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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-alpha-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-alpha, 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物。 流行病学研究表明,许多类型的压力,包括心理社会应激降低端粒长度。 然而,它仍然未知各种压力诱导端粒缩短。 在此,我们报告说应力响应转录因子ATF7介导TNF-α-诱导的端粒缩短。 ATF7和端粒酶,一种伸长端粒的酶,通过与Ku络合物的相互作用局部地局压在端粒上。 响应于TNF-α,其由包括心理应激的各种应力引起的,ATF7被P38磷酸化,导致来自端粒的ATF7和端粒酶的释放。 因此,响应于应力的端粒上的ATF7和端粒酶降低导致端粒缩短,如在ATF7缺陷小鼠中所观察到的。 这些调查结果给予了各种类型的压力可能缩短端粒的想法。

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