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甜菜一种假定糖转运蛋白的分子克隆、液泡免疫化学定位以及在转基因酵母和烟草中的表达

Molecular cloning, immunochemical localization to the vacuole, and expression in transgenic yeast and tobacco of a putative sugar transporter from sugar beet.

作者信息

Chiou T J, Bush D R

机构信息

Department of Plant Biology, University of Illinois, Urbana 61801, USA.

出版信息

Plant Physiol. 1996 Feb;110(2):511-20. doi: 10.1104/pp.110.2.511.

DOI:10.1104/pp.110.2.511
PMID:8742332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC157746/
Abstract

Several plant genes have been cloned that encode members of the sugar transporter subgroup of the major facilitator superfamily of transporters. Here we report the cloning, expression, and membrane localization of one of these porters found in sugar beet (Beta vulgaris L.). This clone, cDNA-1, codes for a protein with 490 amino acids and an estimated molecular mass of 54 kD. The predicted membrane topology and sequence homology suggest that cDNA-1 is a member of the sugar transporter family. RNA gel blot analysis revealed that this putative sugar transporter is expressed in all vegetative tissues and expression increases with development in leaves. DNA gel blot analysis indicated that multiple gene copies exist for this putative sugar transporter in the sugar beet genome. Antibodies directed against small peptides representing the N- and C-terminal domains of the cDNA1 protein identified a 40-kD polypeptide in microsomes isolated from cDNA-1-transformed yeast (Saccharomyces cerevisiae). Moreover, the same protein was identified in sugar beet and transgenic tobacco (Nicotaina tobacum L.) membrane fractions. Detailed analysis of the transporter's distribution across linear sucrose gradients and flotation centrifugations showed that it co-migrates with tonoplast membrane markers. We conclude that this carrier is located on the tonoplast membrane and that it may mediate sugar partitioning between the vacuole and cytoplasmic compartments.

摘要

几个编码转运蛋白主要易化子超家族糖转运蛋白亚组成员的植物基因已被克隆。在此,我们报道在甜菜(Beta vulgaris L.)中发现的其中一个转运蛋白的克隆、表达及膜定位。这个克隆体cDNA - 1编码一个含有490个氨基酸、估计分子量为54 kD的蛋白质。预测的膜拓扑结构和序列同源性表明cDNA - 1是糖转运蛋白家族的成员。RNA凝胶印迹分析显示,这种假定的糖转运蛋白在所有营养组织中均有表达,且在叶片中的表达随发育进程而增加。DNA凝胶印迹分析表明,在甜菜基因组中存在多个该假定糖转运蛋白的基因拷贝。针对代表cDNA1蛋白N端和C端结构域的小肽的抗体,在从cDNA - 1转化酵母(Saccharomyces cerevisiae)中分离出的微粒体中鉴定出一个40 kD的多肽。此外,在甜菜和转基因烟草(Nicotaina tobacum L.)的膜组分中也鉴定出了相同的蛋白。对该转运蛋白在线性蔗糖梯度和浮选离心中分布的详细分析表明,它与液泡膜标记物共同迁移。我们得出结论,这种载体位于液泡膜上,并且它可能介导糖在液泡和细胞质区室之间的分配。

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