Iida M, Murakami T, Ishida K, Mizuno A, Kuwajima M, Shima K
Department of Laboratory Medicine, School of Medicine, University of Tokushima, Japan.
Biochem Biophys Res Commun. 1996 Jul 16;224(2):597-604. doi: 10.1006/bbrc.1996.1070.
We recently cloned one of spliced variant forms of rat leptin receptor (OB-R), which contains a short intracellular domain, and found obese-phenotype-linked nucleotide alteration in the extracellular domain of the cDNA from the Zucker (fa/fa) rat, which results in a glutamine269 to proline269 amino acid substitution. Reported herein are the cloning and sequencing of another spliced variant forms of rat OB-R cDNA with a long intracellular domain. Both forms of OB-R cDNA share the same extracellular domain. In the Zucker (fa/fa) rat, no changes in either the gene structure nor in the nucleotide sequence of the long intracellular domain were observed. However, the expression level of OB-R mRNA in the brain of Zucker (fa/fa) rat was higher than for lean littermates. These facts suggest that the substitution at codon 269 of the OB-R cDNA represents the crucial mutation which results in the obese phenotype of Zucker (fa/fa) rat.
我们最近克隆了大鼠瘦素受体(OB-R)的一种剪接变体形式,其包含一个短的细胞内结构域,并在来自Zucker(fa/fa)大鼠的cDNA的细胞外结构域中发现了与肥胖表型相关的核苷酸改变,这导致了谷氨酰胺269到脯氨酸269的氨基酸替换。本文报道了另一种具有长细胞内结构域的大鼠OB-R cDNA剪接变体形式的克隆和测序。两种形式的OB-R cDNA共享相同的细胞外结构域。在Zucker(fa/fa)大鼠中,未观察到长细胞内结构域的基因结构或核苷酸序列有任何变化。然而,Zucker(fa/fa)大鼠大脑中OB-R mRNA的表达水平高于其瘦的同窝仔。这些事实表明,OB-R cDNA密码子269处的替换代表了导致Zucker(fa/fa)大鼠肥胖表型的关键突变。