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源自通过椎实螺特定神经元VD1和RPD2中单个基因的可变剪接产生的两种相关前激素的肽的加工、轴突运输和心脏调节功能。

Processing, axonal transport and cardioregulatory functions of peptides derived from two related prohormones generated by alternative splicing of a single gene in identified neurons VD1 and RPD2 of Lymnaea.

作者信息

Bogerd J, Li K W, Jiménez C R, van der Schors R C, Ebberink R H, Geraerts W P

机构信息

Graduate School Neurosciences Amsterdam, Research Institute Neurosciences Vrije Universiteit, Faculty of Biology, The Netherlands.

出版信息

Brain Res Mol Brain Res. 1994 Apr;23(1-2):66-72. doi: 10.1016/0169-328x(94)90212-7.

Abstract

The VD1/RPD2 mRNA precursor in identified neurons VD1 and RPD2 of the freshwater snail Lymnaea stagnalis is alternatively spliced to yield two related variants encoding two distinct yet related preprohormones, named the VD1/RPD2-A and -B preprohormones. Here, we report the isolation and structural characterization of alpha 1, alpha 2 and beta peptides from dissected neurons VD1 and RPD2. The alpha 1 and alpha 2 peptides are derived from VD1/RPD2-A and B prohormones, respectively, whereas beta peptide is identical for both prohormones. In addition, we report the isolation and structural characterization of the alpha 2 peptide from the heart, demonstrating that the mature peptides are transported and released in the heart. The pharmacological actions of synthetic alpha 1 and alpha 2 peptides on isolated auricle preparations of the Lymnaea heart were examined. The two alpha peptides have similar excitatory effects on beat rate and beat amplitude, while their potencies differed considerably, indicating that alternative splicing results in structurally and functionally overlapping, through non-identical, sets of peptides.

摘要

淡水螺椎实螺(Lymnaea stagnalis)中已鉴定的神经元VD1和RPD2内的VD1/RPD2信使核糖核酸前体通过可变剪接产生两个相关变体,编码两种不同但相关的前激素原,分别命名为VD1/RPD2 - A和 - B前激素原。在此,我们报告了从解剖的神经元VD1和RPD2中分离出α1、α2和β肽并对其进行结构表征。α1和α2肽分别来自VD1/RPD2 - A和B前激素原,而β肽在两种前激素原中是相同的。此外,我们报告了从心脏中分离出α2肽并对其进行结构表征,证明成熟肽在心脏中运输和释放。研究了合成的α1和α2肽对椎实螺心脏离体心耳制剂的药理作用。这两种α肽对心率和搏动幅度具有相似的兴奋作用,但其效力差异很大,表明可变剪接导致了结构和功能上重叠但不完全相同的肽组。

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