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番茄金属硫蛋白样基因家族的结构、表达及染色体定位

Structure, expression and chromosomal localisation of the metallothionein-like gene family of tomato.

作者信息

Giritch A, Ganal M, Stephan U W, Bäumlein H

机构信息

Institut für Pflanzengenetik und Kulturpflanzenforschung, Gatersleben, Germany.

出版信息

Plant Mol Biol. 1998 Jul;37(4):701-14. doi: 10.1023/a:1006001701919.

Abstract

Metallothioneins are small cysteine-rich proteins with strong binding capacity for heavy metals. In animals and fungi they are involved in cellular detoxification processes. Although genes for similar proteins exist in plants, less is known about the putative functions of their protein products. Here, we describe the characterisation of cDNAs specific for four genes (LEMT1, LEMT2, LEMT3 and LEMT4) encoding metallothionein-like proteins from tomato. Based on the characteristic cysteine pattern, the LEMT1, LEMT3 and LEMT4 gene products represent type 2 proteins. In contrast, the LEMT2 protein might establish a new structural pattern of metallothionein-like proteins not described before. Mapping experiments demonstrate that all four genes are localised at different genetic loci within the tomato genome. The members of the small gene family show a differential organ specific expression pattern. Expression of these genes is also influenced by heavy metals and by treatment with the thiol-oxidising drug diamide. We further describe the expression of the LEMT genes under different iron supply conditions both in tomato wild type as well as in the mutant chloronerva, which is defective in metal uptake regulation and exhibits a characteristic 'apparent iron deficiency syndrome'.

摘要

金属硫蛋白是一类富含半胱氨酸的小蛋白,对重金属具有很强的结合能力。在动物和真菌中,它们参与细胞解毒过程。虽然植物中也存在类似蛋白质的基因,但对其蛋白质产物的假定功能了解较少。在这里,我们描述了来自番茄的四个编码类金属硫蛋白的基因(LEMT1、LEMT2、LEMT3和LEMT4)特异性cDNA的特征。基于特征性的半胱氨酸模式,LEMT1、LEMT3和LEMT4基因产物代表2型蛋白。相比之下,LEMT2蛋白可能建立了一种以前未描述过的类金属硫蛋白新结构模式。定位实验表明,所有四个基因都位于番茄基因组内的不同基因位点。这个小基因家族的成员表现出不同的器官特异性表达模式。这些基因的表达也受到重金属和硫醇氧化药物二酰胺处理的影响。我们进一步描述了LEMT基因在番茄野生型以及突变体chloronerva中不同铁供应条件下的表达情况,突变体chloronerva在金属吸收调节方面存在缺陷,并表现出特征性的“明显缺铁综合征”。

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