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一种新的早衰样综合征表明,基因毒性应激会抑制生长激素轴。

A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis.

作者信息

Niedernhofer Laura J, Garinis George A, Raams Anja, Lalai Astrid S, Robinson Andria Rasile, Appeldoorn Esther, Odijk Hanny, Oostendorp Roos, Ahmad Anwaar, van Leeuwen Wibeke, Theil Arjan F, Vermeulen Wim, van der Horst Gijsbertus T J, Meinecke Peter, Kleijer Wim J, Vijg Jan, Jaspers Nicolaas G J, Hoeijmakers Jan H J

机构信息

Center for Biomedical Genetics Medical Genetic Center Department of Cell Biology and Genetics, Erasmus Medical Center, PO Box 1738, 3000 DR Rotterdam, The Netherlands.

出版信息

Nature. 2006 Dec 21;444(7122):1038-43. doi: 10.1038/nature05456.

Abstract

XPF-ERCC1 endonuclease is required for repair of helix-distorting DNA lesions and cytotoxic DNA interstrand crosslinks. Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum. A patient presented with a severe XPF mutation leading to profound crosslink sensitivity and dramatic progeroid symptoms. It is not known how unrepaired DNA damage accelerates ageing or its relevance to natural ageing. Here we show a highly significant correlation between the liver transcriptome of old mice and a mouse model of this progeroid syndrome. Expression data from XPF-ERCC1-deficient mice indicate increased cell death and anti-oxidant defences, a shift towards anabolism and reduced growth hormone/insulin-like growth factor 1 (IGF1) signalling, a known regulator of lifespan. Similar changes are seen in wild-type mice in response to chronic genotoxic stress, caloric restriction, or with ageing. We conclude that unrepaired cytotoxic DNA damage induces a highly conserved metabolic response mediated by the IGF1/insulin pathway, which re-allocates resources from growth to somatic preservation and life extension. This highlights a causal contribution of DNA damage to ageing and demonstrates that ageing and end-of-life fitness are determined both by stochastic damage, which is the cause of functional decline, and genetics, which determines the rates of damage accumulation and decline.

摘要

XPF-ERCC1核酸内切酶是修复扭曲螺旋的DNA损伤和具有细胞毒性的DNA链间交联所必需的。XPF中的轻度突变会导致易患癌症的着色性干皮病综合征。一名患者出现了严重的XPF突变,导致对交联高度敏感并出现明显的早衰症状。目前尚不清楚未修复的DNA损伤如何加速衰老及其与自然衰老的关联。在此,我们展示了老年小鼠的肝脏转录组与这种早衰综合征小鼠模型之间存在高度显著的相关性。来自XPF-ERCC1缺陷小鼠的表达数据表明细胞死亡增加和抗氧化防御增强,代谢向合成代谢转变,生长激素/胰岛素样生长因子1(IGF1)信号传导减少,而IGF1是已知的寿命调节因子。在野生型小鼠中,对慢性基因毒性应激、热量限制或衰老的反应也会出现类似变化。我们得出结论,未修复的细胞毒性DNA损伤会诱导由IGF1/胰岛素途径介导的高度保守的代谢反应,该反应将资源从生长重新分配到体细胞维持和寿命延长。这突出了DNA损伤对衰老的因果作用,并表明衰老和生命末期的健康状况既由作为功能衰退原因的随机损伤决定,也由决定损伤积累和衰退速率的遗传学决定。

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