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RPN-6 determines C. elegans longevity under proteotoxic stress conditions

机译:RPN-6在蛋白毒性胁迫条件下确定线虫寿命

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摘要

Organisms that protect their germ-cell lineages from damage often do so at considerable cost: limited metabolic resources become partitioned away from maintenance of the soma, leaving the ageing somatic tissues to navigate survival amid an environment containing damaged and poorly functioning proteins. Historically, experimental paradigms that limit reproductive investment result in lifespan extension. We proposed that germline-deficient animals might exhibit heightened protection from proteotoxic stressors in somatic tissues. We find that the forced re-investment of resources from the germ line to the soma in Caenorhabditis elegans results in elevated somatic proteasome activity, clearance of damaged proteins and increased longevity. This activity is associated with increased expression of rpn-6, a subunit of the 19S proteasome, by the FOXO transcription factor DAF-16. Ectopic expression of rpn-6 is sufficient to confer proteotoxic stress resistance and extend lifespan, indicating that rpn-6 is a candidate to correct deficiencies in age-related protein homeostasis disorders.
机译:保护其生殖细胞谱系免受损害的有机体通常会付出可观的代价:有限的新陈代谢资源从维持体细胞中分离出来,使老化的体细胞组织在蛋白质受损且功能差的环境中导航生存。从历史上看,限制生殖投资的实验范式导致寿命的延长。我们提出种系缺陷的动物可能对体组织中的蛋白毒性应激物表现出更高的保护作用。我们发现,秀丽隐杆线虫从种系到体细胞的强制性资源再投资会导致体细胞蛋白酶体活性升高,清除受损蛋白并延长寿命。此活性与FOXO转录因子DAF-16增强的19S蛋白酶体亚基rpn-6的表达有关。 rpn-6的异位表达足以赋予蛋白毒性应激抗性并延长寿命,这表明rpn-6是纠正与年龄有关的蛋白质体内稳态疾病缺陷的候选药物。

著录项

  • 来源
    《Nature》 |2012年第7415期|p.263-268|共6页
  • 作者单位

    Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA;

    Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA;

    Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA;

    Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA;

    Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA;

    Razavi Newman Center for Bioinformatics, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA,Department of Computational Medicine and Bioinformatics, University of Michigan, 100 Washtenaw Avenue, Ann Arbor, Michigan 48109-2218, USA;

    Razavi Newman Center for Bioinformatics, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA,Bioinformatics and Computational Biology, Genentech, 1 DNA Way, South San Francisco, California 94080, USA;

    Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:54:16

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