TY - CHAP
T1 - Studies on the very large G protein-coupled receptor
T2 - From initial discovery to determining its role in sensorineural deafness in higher animals
AU - McMillan, D. Randy
AU - White, Perrin C.
PY - 2010/12/1
Y1 - 2010/12/1
N2 - The very large G protein-coupled receptor 1 (VLGR1), also known as MASS1 or GPR98, is most notable among the family of adhesion-GPCR for its size. Encoded by an 18.9 kb open reading frame, the ∼700 kDa primary translation product is by far the largest GPCR and additionally, the largest cell surface protein known to date. The large ectodomain of the protein contains several repeated motifs, including some 35 calcium binding, Calx-β repeats and seven copies of an epitempin repeat thought to be associated with the development of epilepsy. The extreme carboxy-terminus contains a consensus PDZ ligand sequence, suggesting interactions with other cytosolic or cytoskeletal proteins. At least two spontaneous and two targeted mutant mouse lines are currently known. The mutant mice present with sensitivity to audiogenic seizures but also have cochlear defects and significant, progressive hearing impairment. Although its ligand is currently unknown, VLGR1 is one of the few adhesion-GPCR family members in which mutations have been shown to be responsible for a human malady. Mutations in VLGR1 in humans result in one form (2C) of Usher syndrome, the most common genetic cause of combined blindness and deafness.
AB - The very large G protein-coupled receptor 1 (VLGR1), also known as MASS1 or GPR98, is most notable among the family of adhesion-GPCR for its size. Encoded by an 18.9 kb open reading frame, the ∼700 kDa primary translation product is by far the largest GPCR and additionally, the largest cell surface protein known to date. The large ectodomain of the protein contains several repeated motifs, including some 35 calcium binding, Calx-β repeats and seven copies of an epitempin repeat thought to be associated with the development of epilepsy. The extreme carboxy-terminus contains a consensus PDZ ligand sequence, suggesting interactions with other cytosolic or cytoskeletal proteins. At least two spontaneous and two targeted mutant mouse lines are currently known. The mutant mice present with sensitivity to audiogenic seizures but also have cochlear defects and significant, progressive hearing impairment. Although its ligand is currently unknown, VLGR1 is one of the few adhesion-GPCR family members in which mutations have been shown to be responsible for a human malady. Mutations in VLGR1 in humans result in one form (2C) of Usher syndrome, the most common genetic cause of combined blindness and deafness.
UR - http://www.scopus.com/inward/record.url?scp=79960795399&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79960795399&partnerID=8YFLogxK
U2 - 10.1007/978-1-4419-7913-1_6
DO - 10.1007/978-1-4419-7913-1_6
M3 - Chapter
C2 - 21618827
AN - SCOPUS:79960795399
SN - 9781441979124
T3 - Advances in Experimental Medicine and Biology
SP - 76
EP - 86
BT - Adhesion-GPCRs
A2 - Yona, Simon
A2 - Stacey, Martin
ER -