Progress in demystification of adhesion G protein-coupled receptors

被引:42
作者
Liebscher, Ines [1 ]
Schoeneberg, Torsten [1 ]
Proemel, Simone [1 ]
机构
[1] Univ Leipzig, Fac Med, Inst Biochem, D-04103 Leipzig, Germany
关键词
adhesion GPCR; autocatalytic cleavage; G protein; signaling mechanisms; trans and cis signaling; PLANAR CELL POLARITY; BRAIN ANGIOGENESIS INHIBITOR-1; V-2 VASOPRESSIN RECEPTOR; GENOME-WIDE ASSOCIATION; CONSTITUTIVE ACTIVITY; EXTRACELLULAR DOMAIN; ALPHA-LATROTOXIN; STRUCTURAL REQUIREMENTS; TRANSMEMBRANE RECEPTOR; PROTEOLYTIC CLEAVAGE;
D O I
10.1515/hsz-2013-0109
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
Adhesion G protein-coupled receptors (aGPCR) form the second largest class of GPCR. They are phylogenetically old and have been highly conserved during evolution. Mutations in representatives of this class are associated with severe diseases such as Usher Syndrome, a combined congenital deaf-blindness, or bifrontal parietal polymicrogyria. The main characteristics of aGPCR are their enormous size and the complexity of their N termini. They contain a highly conserved GPCR proteolytic site (GPS) and several functional domains that have been implicated in cell-cell and cell-matrix interactions. Adhesion GPCR have been proposed to serve a dual function as adhesion molecules and as classical receptors. However, until recently there was no proof that aGPCR indeed couple to G proteins or even function as classical receptors. In this review, we have summarized and discussed recent evidence that aGPCR present many functional features of classical GPCR, including multiple G protein-coupling abilities, G protein-independent signaling and oligomerization, but also specific signaling properties only found in aGPCR.
引用
收藏
页码:937 / 950
页数:14
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