Lee Sung Bae, Kim Sunhong, Lee Jiwoon, Park Jeehye, Lee Gina, Kim Yongsung, Kim Jin-Man, Chung Jongkyeong
National Creative Research Initiatives Center for Cell Growth Regulation, Department of Biological Sciences, Korea Advanced Institute of Science and Technology, 373-1 Kusong-dong, Yusong-gu, Taejon 305-701, Republic of Korea.
EMBO Rep. 2007 Apr;8(4):360-5. doi: 10.1038/sj.embor.7400917. Epub 2007 Mar 9.
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.
有人提出,细胞生长和自噬会根据细胞营养状态进行协调,但它们之间的关系尚未完全明确。在此,我们对自噬特异性基因1(ATG1,一种自噬调节激酶)的果蝇突变体进行了表征,发现ATG1是雷帕霉素靶蛋白(TOR)/S6激酶(S6K)信号通路的负调节因子。我们的果蝇研究表明,ATG1通过干扰S6K的激活来抑制TOR/S6K依赖的细胞生长和发育。同样,在哺乳动物细胞中过表达ATG1也会以激酶活性依赖的方式显著抑制S6K,而短干扰RNA介导的ATG1敲低会诱导S6K的异位激活和S6磷酸化。此外,我们证明ATG1通过阻断S6K在苏氨酸389处的磷酸化来特异性抑制S6K活性。综上所述,我们的遗传和生化结果有力地表明自噬与细胞生长调节之间存在相互作用。