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

被引:130
作者
Lee, Sung Bae
Kim, Sunhong
Lee, Jiwoon
Park, Jeehye
Lee, Gina
Kim, Yongsung
Kim, Jin-Man
Chung, Jongkyeong
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Natl Creat Res Initiat Ctr Cell Growth Regulat, Taejon 305701, South Korea
[2] Chungnam Natl Univ, Sch Med, Dept Pathol, Taejon 301721, South Korea
关键词
autophagy; cell growth; S6K; TOR;
D O I
10.1038/sj.embor.7400917
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:360 / 365
页数:6
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