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来自野豌豆萌发种子的编码半胱氨酸蛋白酶的cDNA的PCR克隆及表达分析

PCR cloning and expression analysis of cDNAs encoding cysteine proteinases from germinating seeds of Vicia sativa L.

作者信息

Becker C, Fischer J, Nong V H, Münitz K

机构信息

Institut für Pflanzengenetik und Kulturpflanzenforshung, Gatersleben, Germany.

出版信息

Plant Mol Biol. 1994 Nov;26(4):1207-12. doi: 10.1007/BF00040701.

Abstract

cDNA clones encoding cysteine proteinases from cotyledons of germinated seeds of Vicia sativa L. have been obtained by means of PCR. Degenerate oligonucleotide primers were designed according to conserved amino acid regions of known cysteine proteinases. The deduced amino acid sequences of the cDNA clones encoding VSCYSPR1 and VSCYSPR2 display strong homology to cysteine proteinases of the so called papain superfamily. Northern analyses revealed developmentally regulated expression of both the mRNAs in germinating seeds. The transcripts were shown to be products of two distinct single genes, each exhibiting structural polymorphisms as exposed in few nucleotide substitutions.

摘要

通过聚合酶链反应(PCR)已从蚕豆发芽种子的子叶中获得了编码半胱氨酸蛋白酶的互补脱氧核糖核酸(cDNA)克隆。根据已知半胱氨酸蛋白酶的保守氨基酸区域设计了简并寡核苷酸引物。编码VSCYSPR1和VSCYSPR2的cDNA克隆推导的氨基酸序列与所谓木瓜蛋白酶超家族的半胱氨酸蛋白酶具有很强的同源性。Northern分析显示,在发芽种子中这两种信使核糖核酸(mRNA)的表达受发育调控。这些转录本显示是两个不同单基因的产物,每个基因在少数核苷酸取代中表现出结构多态性。

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