TY - JOUR
T1 - Pleiotropic phenotype of a genomic knock-in of an RGS-insensitive G184S Gnai2 allele
AU - Huang, Xinyan
AU - Fu, Ying
AU - Charbeneau, Raelene A.
AU - Saunders, Thomas L.
AU - Taylor, Douglas K.
AU - Hankenson, Kurt D.
AU - Russell, Mark W.
AU - D'Alecy, Louis G.
AU - Neubig, Richard R.
PY - 2006/9
Y1 - 2006/9
N2 - Signal transduction via guanine nucleotide binding proteins (G proteins) is involved in cardiovascular, neural, endocrine, and immune cell function. Regulators of G protein signaling (RGS proteins) speed the turn-off of G protein signals and inhibit signal transduction, but the in vivo roles of RGS proteins remain poorly defined. To overcome the redundancy of RGS functions and reveal the total contribution of RGS regulation at the Gαi2 subunit, we prepared a genomic knock-in of the RGS-insensitive G184S Gnai2 allele. The Gαi2G184S knock-in mice show a dramatic and complex phenotype affecting multiple organ systems (heart, myeloid, skeletal, and central nervous system). Both homozygotes and heterozygotes demonstrate reduced viability and decreased body weight. Other phenotypes include shortened long bones, a markedly enlarged spleen, elevated neutrophil counts, an enlarged heart, and behavioral hyperactivity. Heterozygous Gα12 +/G184S mice show some but not all of these abnormalities. Thus, loss of RGS actions at Gα12 produces a dramatic and pleiotropic phenotype which is more evident than the phenotype seen for individual RGS protein knockouts.
AB - Signal transduction via guanine nucleotide binding proteins (G proteins) is involved in cardiovascular, neural, endocrine, and immune cell function. Regulators of G protein signaling (RGS proteins) speed the turn-off of G protein signals and inhibit signal transduction, but the in vivo roles of RGS proteins remain poorly defined. To overcome the redundancy of RGS functions and reveal the total contribution of RGS regulation at the Gαi2 subunit, we prepared a genomic knock-in of the RGS-insensitive G184S Gnai2 allele. The Gαi2G184S knock-in mice show a dramatic and complex phenotype affecting multiple organ systems (heart, myeloid, skeletal, and central nervous system). Both homozygotes and heterozygotes demonstrate reduced viability and decreased body weight. Other phenotypes include shortened long bones, a markedly enlarged spleen, elevated neutrophil counts, an enlarged heart, and behavioral hyperactivity. Heterozygous Gα12 +/G184S mice show some but not all of these abnormalities. Thus, loss of RGS actions at Gα12 produces a dramatic and pleiotropic phenotype which is more evident than the phenotype seen for individual RGS protein knockouts.
UR - http://www.scopus.com/inward/record.url?scp=33748676137&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33748676137&partnerID=8YFLogxK
U2 - 10.1128/MCB.00314-06
DO - 10.1128/MCB.00314-06
M3 - Article
C2 - 16943428
AN - SCOPUS:33748676137
SN - 0270-7306
VL - 26
SP - 6870
EP - 6879
JO - Molecular and Cellular Biology
JF - Molecular and Cellular Biology
IS - 18
ER -