Heterotrimeric G protein signaling via GIV/Girdin: Breaking the rules of engagement, space, and time

被引:36
作者
Aznar, Nicolas [1 ]
Kalogriopoulos, Nicholas [1 ]
Midde, Krishna K. [1 ]
Ghosh, Pradipta [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Cell & Mol Med, La Jolla, CA 92093 USA
关键词
autophagy; cdk5: Girdin; Golgi; growth factor receptor tyrosine kinases; heterotrimeric G proteins; GUANINE-NUCLEOTIDE EXCHANGE; RESONANCE ENERGY-TRANSFER; GROWTH-FACTOR RECEPTOR; G-ALPHA-I; CONTROLS AUTOPHAGIC SEQUESTRATION; GTPASE-ACTIVATING PROTEIN; RAS-RELATED PROTEIN; LIVING CELLS; INTRINSIC DISORDER; CANCER CELLS;
D O I
10.1002/bies.201500133
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
Canonical signal transduction via heterotrimeric G proteins is spatially and temporally restricted, that is, triggered exclusively at the plasma membrane (PM), only by agonist activation of G protein-coupled receptors (GPCRs) via a process that completes within a few hundred milliseconds. Recently, a rapidly emerging paradigm has revealed a non-canonical pathway for activation of heterotrimeric G proteins by the non-receptor guanidine-nucleotide exchange factor (GEF), GIV/Girdin. This pathway has distinctive temporal and spatial features and an unusual profile of receptor engagement: diverse classes of receptors, not just GPCRs can engage with GIV to trigger such activation. Such activation is spatially and temporally unrestricted, that is, can occur both at the PM and on internal membranes discontinuous with the PM, and can continue for prolonged periods of time. Here, we provide the most complete up-to-date review of the molecular mechanisms that govern the unique spatiotemporal aspects of non-canonical G protein activation by GIV and the relevance of this new paradigm in health and disease.
引用
收藏
页码:379 / 393
页数:15
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