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从大豆(Glycine max)DNA文库中分离出的两个Ypt/Rab相关序列的分子分析。

Molecular analysis of two Ypt/Rab-related sequences isolated from soybean (Glycine max) DNA libraries.

作者信息

Borg S, Poulsen C

机构信息

Department of Molecular Biology, University of Aarhus, Denmark.

出版信息

Plant Mol Biol. 1994 Oct;26(1):175-87. doi: 10.1007/BF00039530.

Abstract

From nodule and seedling cDNA libraries we isolated cDNA copies of two mRNAs, derived from the genes gmr1 and gmr2, encoding members of the Ypt/Rab family of small GTP-binding proteins. Two deduced protein products, GMR1 and GMR2, were found to be nearly identical differing by only four amino acids in the analysed parts. The two putative proteins are 79% identical to the previously described ARA small GTPase from Arabidopsis thaliana. The GMR proteins may thus be the counterpart of the ARA protein and may perform a related biological function in Glycine max. The gmr2 genomic sequence was isolated and structurally analysed. Expression analyses by northern and cDNA-based PCR showed that the gmr1 and gmr2 genes are constitutively expressed in different plant organs, although at a slightly higher level in callus culture. The classification of the gmr sequences as relatives of the Ypt/Rab family suggests that the deduced GMR proteins are involved in control of processes related to vesicle trafficking in plant cells.

摘要

从根瘤和幼苗cDNA文库中,我们分离出了两个mRNA的cDNA拷贝,它们分别来源于基因gmr1和gmr2,这两个基因编码小GTP结合蛋白Ypt/Rab家族的成员。我们发现,两个推导的蛋白质产物GMR1和GMR2几乎完全相同,在分析的部分中仅相差四个氨基酸。这两个推定的蛋白质与先前描述的拟南芥ARA小GTP酶有79%的同一性。因此,GMR蛋白可能是ARA蛋白的对应物,并可能在大豆中执行相关的生物学功能。我们分离出了gmr2基因组序列并进行了结构分析。通过Northern杂交和基于cDNA的PCR进行的表达分析表明,gmr1和gmr2基因在不同的植物器官中组成型表达,尽管在愈伤组织培养中的表达水平略高。将gmr序列归类为Ypt/Rab家族的亲属表明,推导的GMR蛋白参与了植物细胞中与囊泡运输相关的过程的控制。

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