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人μ阿片受体mRNA的两种变体在SK-N-SH细胞和人脑中的表达。

Expression of two variants of the human mu opioid receptor mRNA in SK-N-SH cells and human brain.

作者信息

Bare L A, Mansson E, Yang D

机构信息

Ohmeda PPD, Murray Hill, NJ 07974.

出版信息

FEBS Lett. 1994 Nov 7;354(2):213-6. doi: 10.1016/0014-5793(94)01129-x.

Abstract

A partial mu opioid receptor gene was isolated from a human genomic library using a mouse delta opioid receptor cDNA as a probe. Using information from this genomic clone and the published human mu receptor, MOR1, a cDNA was isolated from SK-N-SH mRNA that codes for a variant of the MOR1 mRNA, MOR1A. The presence of MOR1A is also shown in human brain using RT-PCR. MOR1A differs from MOR1 in that the 3' terminal intron has not been removed. An in-frame termination codon is found four amino acids after the 5' consensus splice site, making MOR1A eight amino acids shorter than MOR1. Both receptors show similar ligand binding and coupling to cAMP in CHO-K1 cells. The C-terminal differences between MOR1 and MOR1A could have effects on receptor coupling or receptor transport and localization.

摘要

使用小鼠δ阿片受体cDNA作为探针,从人基因组文库中分离出部分μ阿片受体基因。利用该基因组克隆和已发表的人μ受体MOR1的信息,从SK-N-SH mRNA中分离出一个cDNA,其编码MOR1 mRNA的变体MOR1A。利用逆转录聚合酶链反应(RT-PCR)也证明了人脑中存在MOR1A。MOR1A与MOR1的不同之处在于其3'末端内含子未被去除。在5'共有剪接位点后的四个氨基酸处发现了一个框内终止密码子,使得MOR1A比MOR1短八个氨基酸。两种受体在CHO-K1细胞中显示出相似的配体结合以及与环磷酸腺苷(cAMP)的偶联。MOR1和MOR1A之间的C末端差异可能会对受体偶联或受体转运及定位产生影响。

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