Jaber M, Koch W J, Rockman H, Smith B, Bond R A, Sulik K K, Ross J, Lefkowitz R J, Caron M G, Giros B
Howard Hughes Medical Institute Laboratories, Duke University Medical Center, Durham, NC 27710, USA.
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):12974-9. doi: 10.1073/pnas.93.23.12974.
The beta-adrenergic receptor kinase 1 (beta ARK1) is a member of the G protein-coupled receptor kinase (GRK) family that mediates the agonist-dependent phosphorylation and desensitization of G protein-coupled receptors. We have cloned and disrupted the beta ARK1 gene in mice by homologous recombination. No homozygote beta ARK1-/- embryos survive beyond gestational day 15.5. Prior to gestational day 15.5, beta ARK1-/- embryos display pronounced hypoplasia of the ventricular myocardium essentially identical to the "thin myocardium syndrome" observed upon gene inactivation of several transcription factors (RXR alpha, N-myc, TEF-1, WT-1). Lethality in beta ARK1-/- embryos is likely due to heart failure as they exhibit a > 70% decrease in cardiac ejection fraction determined by direct in utero intravital microscopy. These results along with the virtual absence of endogenous GRK activity in beta ARK1-/- embryos demonstrate that beta ARK1 appears to be the predominant GRK in early embryogenesis and that it plays a fundamental role in cardiac development.
β-肾上腺素能受体激酶1(βARK1)是G蛋白偶联受体激酶(GRK)家族的成员,介导G蛋白偶联受体的激动剂依赖性磷酸化和脱敏。我们通过同源重组在小鼠中克隆并破坏了βARK1基因。没有纯合子βARK1-/-胚胎能存活超过妊娠第15.5天。在妊娠第15.5天之前,βARK1-/-胚胎表现出明显的心室心肌发育不全,这与在几种转录因子(RXRα、N-myc、TEF-1、WT-1)基因失活后观察到的“薄心肌综合征”基本相同。βARK1-/-胚胎的致死性可能是由于心力衰竭,因为通过直接子宫内活体显微镜检查确定它们的心脏射血分数降低了70%以上。这些结果以及βARK1-/-胚胎中几乎没有内源性GRK活性表明,βARK1似乎是早期胚胎发育中的主要GRK,并且它在心脏发育中起基本作用。