Evolution of Atg1 function and regulation

被引:112
作者
Chan, Edmond Y. [2 ]
Tooze, Sharon A. [1 ]
机构
[1] Canc Res UK, London Res Inst, London WC2A 3PX, England
[2] Univ Strathclyde, Inst Pharm & Biomed Sci, Glasgow, Lanark, Scotland
关键词
ULK; unc-51; unc-51-like kinase; fused; STK36; autophagy; PRE-AUTOPHAGOSOMAL STRUCTURE; STARVATION-INDUCED AUTOPHAGY; INHIBITS CELL-GROWTH; C-ELEGANS; CAENORHABDITIS-ELEGANS; PROTEIN-KINASE; SERINE/THREONINE KINASE; SACCHAROMYCES-CEREVISIAE; SELECTIVE AUTOPHAGY; YEAST AUTOPHAGY;
D O I
10.4161/auto.8709
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The serine/threonine kinase Atg1 plays an essential role downstream of TOR for the regulation of autophagy. In yeast, where Atg1 was first identified, a complex regulatory mechanism has been described that includes at least seven other interacting proteins and a phosphorylation-dependent switch. Recent findings confirm that the mammalian Atg1 homologues ULK1 and 2 have autophagy regulatory roles. However, we and others have also demonstrated mechanistic differences with the yeast model and between these two Atg1 family members. Here, we elaborate on our growing understanding of Atg1 function, incorporating findings from yeast, C elegans, D. melanogaster and mammalian cells. We propose that through evolution, Atg1 proteins have adopted additional cellular functions and regulatory mechanisms, which could involve multiple gene family isoforms working within multifunctional protein complexes. The gene family expansion observed in higher eukaryotes might reflect an increased functional diversity of Atg1 proteins in cell growth, differentiation and survival.
引用
收藏
页码:758 / 765
页数:8
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