Minakami R, Katsuki F, Sugiyama H
Department of Biology, Faculty of Science, Kyushu University, Fukuoka, Japan.
Biochem Biophys Res Commun. 1993 Jul 30;194(2):622-7. doi: 10.1006/bbrc.1993.1866.
We herein report the presence of a variant of the rat metabotropic glutamate receptor subtype 5 (mGluR5) cDNA. In this variant, named mGluR5b, an extra 96 bp sequence is inserted into the originally reported mGluR5 cDNA. The position of this insertion corresponds to that of the 85 bp insertion reported for the alternative form of mGluR1, another subtype of the receptors (designated as mGluR1 beta). No sequence-similarity was found between the additional sequences of the mGluR1 beta and the mGluR5b. While the additional sequence of the mGluR1 beta cDNA contains a translation termination codon in the frame, that of the mGluR5b cDNA does not. This identical 96 bp insertion was also found in a human mGluR5 cDNA clone. Northern blot analyses with the mGluR5b-specific probe showed that the expression of mRNA for this species is regulated in a region-specific manner in the rat brain.
我们在此报告大鼠代谢型谷氨酸受体5(mGluR5)cDNA存在一种变体。在这种名为mGluR5b的变体中,一段额外的96bp序列插入到最初报道的mGluR5 cDNA中。该插入位置与报道的另一种受体亚型(称为mGluR1β)的mGluR1替代形式中85bp插入的位置相对应。在mGluR1β和mGluR5b的额外序列之间未发现序列相似性。虽然mGluR1β cDNA的额外序列在阅读框中包含一个翻译终止密码子,但mGluR5b cDNA的额外序列中没有。在一个人类mGluR5 cDNA克隆中也发现了这个相同的96bp插入。用mGluR5b特异性探针进行的Northern印迹分析表明,该物种mRNA的表达在大鼠脑中以区域特异性方式受到调节。