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A genetic program mediates cold-warming response and promotes stress-induced phenoptosis in C. elegans

机译:遗传程序介导冷暖反应并促进秀丽隐杆线虫的应激诱导的表皮凋亡

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摘要

How multicellular organisms respond to and are impacted by severe hypothermic stress is largely unknown. From C. elegans screens for mutants abnormally responding to cold-warming stimuli, we identify a molecular genetic pathway comprising ISY-1, a conserved uncharacterized protein, and ZIP-10, a bZIP-type transcription factor. ISY-1 gatekeeps the ZIP-10 transcriptional program by regulating the microRNA mir-60. Downstream of ISY-1 and mir-60, zip-10 levels rapidly and specifically increase upon transient cold-warming exposure. Prolonged zip-10 up-regulation induces several protease-encoding genes and promotes stress-induced organismic death, or phenoptosis, of C. elegans. zip-10 deficiency confers enhanced resistance to prolonged cold-warming stress, more prominently in adults than larvae. We conclude that the ZIP-10 genetic program mediates cold-warming response and may have evolved to promote wild-population kin selection under resource-limiting and thermal stress conditions.
机译:多细胞生物如何应对严重的低温应激并受到其影响尚不清楚。从秀丽隐杆线虫筛选异常响应冷暖刺激突变体,我们确定分子遗传途径包括ISY-1,一种保守的未表征的蛋白质,和ZIP-10,一种bZIP型转录因子。 ISY-1通过调节microRNA mir-60来控制ZIP-10转录程序。在ISY-1和mir-60下游,zip-10水平迅速升高,并且在短暂的冷暖暴露后会特别升高。长期的zip-10上调诱导了几种蛋白酶编码基因,并促进了应激诱导的秀丽隐杆线虫的生物死亡或表皮凋亡。 zip-10缺乏症可增强对延长的冷暖应激的抵抗力,在成年人中比幼虫更为突出。我们得出的结论是,ZIP-10遗传程序介导了冷暖反应,并且可能已经进化为在资源有限和热胁迫条件下促进野生种群亲缘选择。

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