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编码尾加压素I前体的cDNA的克隆与序列分析

Cloning and sequence analysis of cDNA encoding urotensin I precursor.

作者信息

Ishida I, Ichikawa T, Deguchi T

出版信息

Proc Natl Acad Sci U S A. 1986 Jan;83(2):308-12. doi: 10.1073/pnas.83.2.308.

Abstract

The primary structure of the precursor of urotensin I, a neuropeptide hormone from the caudal neurosecretory system of the carp Cyprinus carpio, has been determined by analyzing the nucleotide sequence of cloned DNA complementary to the mRNA encoding it. The precursor consists of 145 amino acid residues and the carboxyl terminus represents the 41-amino acid sequence of urotensin I, preceded by Lys-Arg and followed by Gly-Lys. Sequence homology as well as similar organization of the precursors of urotensin I and mammalian corticotropin-releasing factors suggest that they are evolutionarily related. RNA transfer blot analysis indicates that mRNA encoding the precursor of urotensin I is present only in the spinal cord and not in the brain, intestine, liver, or kidney of the carp.

摘要

通过分析与编码urotensin I的mRNA互补的克隆DNA的核苷酸序列,已确定了鲤鱼尾神经分泌系统中神经肽激素urotensin I前体的一级结构。该前体由145个氨基酸残基组成,其羧基末端代表urotensin I的41个氨基酸序列,前面是Lys-Arg,后面是Gly-Lys。urotensin I前体与哺乳动物促肾上腺皮质激素释放因子的序列同源性以及相似的结构组织表明它们在进化上相关。RNA转移印迹分析表明,编码urotensin I前体的mRNA仅存在于鲤鱼的脊髓中,而不存在于其脑、肠、肝或肾中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c236/322847/adbe3820db03/pnas00306-0119-a.jpg

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