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ATG1 an autophagy regulator inhibits cell growth by negatively regulating S6 kinase

机译:自噬调节剂ATG1通过负调节S6激酶抑制细胞生长

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摘要

It has been proposed that cell growth and autophagy are coordinated in response to cellular nutrient status, but the relationship between them is not fully understood. Here, we have characterized the fly mutants of Autophagy-specific gene 1 (ATG1), an autophagy-regulating kinase, and found that ATG1 is a negative regulator of the target of rapamycin (TOR)/S6 kinase (S6K) pathway. Our Drosophila studies have shown that ATG1 inhibits TOR/S6K-dependent cell growth and development by interfering with S6K activation. Consistently, overexpression of ATG1 in mammalian cells also markedly inhibits S6K in a kinase activity-dependent manner, and short interfering RNA-mediated knockdown of ATG1 induces ectopic activation of S6K and S6 phosphorylation. Moreover, we demonstrated that ATG1 specifically inhibits S6K activity by blocking phosphorylation of S6K at Thr 389. Taken together, our genetic and biochemical results strongly indicate crosstalk between autophagy and cell growth regulation.
机译:已经提出细胞生长和自噬响应于细胞营养状况而协调,但是它们之间的关系尚未完全理解。在这里,我们已经表征了自噬特异性基因1(ATG1)的蝇突变体,一种自噬调节激酶,并且发现ATG1是雷帕霉素(TOR)/ S6激酶(S6K)途径靶标的负调节剂。我们的果蝇研究表明,ATG1通过干扰S6K激活来抑制TOR / S6K依赖性细胞的生长和发育。一致地,哺乳动物细胞中ATG1的过表达还以激酶活性依赖性方式显着抑制S6K,而RNA介导的ATG1的短干扰抑制诱导S6K和S6磷酸化的异位激活。此外,我们证明了ATG1通过在Thr 389处阻断S6K的磷酸化而特异性抑制S6K活性。综上,我们的遗传和生化结果强烈表明自噬与细胞生长调节之间的串扰。

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