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通过可变剪接鉴定小鼠神经肽Y-Y1受体的两种亚型。受体的分离、基因组结构及功能表达。

Identification of two isoforms of mouse neuropeptide Y-Y1 receptor generated by alternative splicing. Isolation, genomic structure, and functional expression of the receptors.

作者信息

Nakamura M, Sakanaka C, Aoki Y, Ogasawara H, Tsuji T, Kodama H, Matsumoto T, Shimizu T, Noma M

机构信息

Life Science Research Laboratory, Japan Tobacco Inc., Kanagawa, Japan.

出版信息

J Biol Chem. 1995 Dec 15;270(50):30102-10. doi: 10.1074/jbc.270.50.30102.

Abstract

Two cDNA clones homologous with human neuropeptide (NP) Y-Y1 receptor have been isolated from a mouse bone marrow cDNA library. One was thought to be the cognate of the human NPY-Y1 receptor, termed Y1 alpha receptor, and the other form, termed Y1 beta receptor, differed from the Y1 alpha receptor in the seventh transmembrane domain and C-terminal tail. Analysis of the mouse genomic DNA showed that both receptors originated from a single gene. The different peptide sequences of the Y1 beta receptor were encoded by separate exons, hence, these receptors were generated by differential RNA splicing. High affinity binding of [125I]NPY to each receptor expressed in Chinese hamster ovary (CHO) cells and sequestration of [125I]NPY after binding to each receptor were observed. In the CHO cells expressing the Y1 alpha receptor, intracellular Ca2+ increase, inhibition of forskolin-induced cAMP accumulation, and mitogen-activated protein kinase (MAPK) activation were observed by stimulation of NPY, and these responses were abolished by pretreatment with pertussis toxin. Since wortmannin completely inhibited NPY-elicited MAPK activation, we speculate that wortmannin-sensitive signaling molecule(s) such as phosphoinositide 3-kinase may lie between pertussis toxin-sensitive G-protein and MAPK. In contrast, these intracellular signals were not detected in CHO cells expressing the Y1 beta receptor. Northern blots and reverse transcriptase-polymerase chain reaction analyses indicated that the Y1 alpha receptor was highly expressed in the brain, heart, kidney, spleen, skeletal muscle, and lung, whereas the Y1 beta receptor mRNA was not detected in these tissues. However, the Y1 beta receptor was expressed in mouse embryonic developmental stage (7 and 11 days), bone marrow cells and several hematopoietic cell lines. These results suggest that the Y1 beta receptor is an embryonic and a bone marrow form of the NPY-Y1 receptor, which decreases in the expression during development and differentiation.

摘要

从一个小鼠骨髓cDNA文库中分离出了两个与人神经肽(NP)Y-Y1受体同源的cDNA克隆。其中一个被认为是人类NPY-Y1受体的同源物,称为Y1α受体,另一种形式称为Y1β受体,它在第七个跨膜结构域和C末端尾巴上与Y1α受体不同。对小鼠基因组DNA的分析表明,这两种受体都起源于一个单一基因。Y1β受体的不同肽序列由不同的外显子编码,因此,这些受体是通过差异RNA剪接产生的。观察到[125I]NPY与中国仓鼠卵巢(CHO)细胞中表达的每种受体的高亲和力结合以及结合到每种受体后[125I]NPY的滞留。在表达Y1α受体的CHO细胞中,通过刺激NPY观察到细胞内Ca2+增加、福司可林诱导的cAMP积累受到抑制以及丝裂原活化蛋白激酶(MAPK)激活,并且这些反应通过百日咳毒素预处理而被消除。由于渥曼青霉素完全抑制了NPY诱导的MAPK激活,我们推测渥曼青霉素敏感的信号分子如磷脂酰肌醇3激酶可能位于百日咳毒素敏感的G蛋白和MAPK之间。相反,在表达Y1β受体的CHO细胞中未检测到这些细胞内信号。Northern印迹和逆转录聚合酶链反应分析表明,Y1α受体在脑、心脏、肾脏、脾脏、骨骼肌和肺中高表达,而在这些组织中未检测到Y1β受体mRNA。然而,Y1β受体在小鼠胚胎发育阶段(7天和11天)、骨髓细胞和几种造血细胞系中表达。这些结果表明,Y1β受体是NPY-Y1受体的胚胎形式和骨髓形式,其在发育和分化过程中表达减少。

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