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Structural and functional analysis of a salt stress inducible gene encoding voltage dependent anion channel (VDAC) from pearl millet (Pennisetum glaucum)

机译:盐胁迫诱导的编码小米(Pennisetum glaucum)电压依赖性阴离子通道(VDAC)的基因的结构和功能分析

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We have cloned and characterized a gene encoding voltage-dependent anion channel from Pennisetum glaucum (PgVDAC). PgVDAC was identified while isolating genes that were differentially up-regulated following salt stress. The genomic organization of PgVDAC clone was well conserved compared to other plant VDAC genes in terms of number of introns, their position and phasing, however, the primary amino acid sequence of voltage dependent anion channel (VDAC) proteins did not show much conservation with other plant VDACs but their secondary and tertiary structures are well conserved as predicted by in silico structural and CD spectra analyses and results show it to be a typical membrane-spanning P-barrel leading to the formation of pore in the membrane. The heterologous expression of PgVDAC protein in yeast strain lacking the endogenous mitochondrial VDAC gene could not functionally complement it as was also previously observed for the potato VDAC. Using realtime quantitative PCR analysis it was found that transcript expression profile of PgVDAC was quantitatively and kinetically up-regulated in response to salinity, desiccation, cold and exogenous application of salicylic acid (SA); however, there was no effect of exogenous application of abscisic acid (ABA) on its expression. Constitutive over-expression of PgVDAC appears to be deleterious in transgenic rice plant; however, low level of up-regulation imparted salinity stress adaptive response. A search for a more suitable inducible transgene system is currently under way to understand PgVDAC expression levels in plant development and its role in stress adaptation. (c) 2006 Elsevier Masson SAS. All rights reserved.
机译:我们已经克隆和表征了编码青草狼尾草(PgVDAC)的电压依赖性阴离子通道的基因。在分离盐胁迫后差异上调的基因时,鉴定出PgVDAC。与其他植物VDAC基因相比,PgVDAC克隆的基因组组织在内含子数量,位置和定相方面都非常保守,但是,电压依赖性阴离子通道(VDAC)蛋白的主要氨基酸序列与其他植物相比没有太多保守性植物VDAC,但通过计算机模拟结构和CD光谱分析预测,它们的二级和三级结构保存良好,结果表明它是典型的跨膜P桶,导致在膜中形成孔。在缺乏内源性线粒体VDAC基因的酵母菌株中,PgVDAC蛋白的异源表达无法对其功能进行互补,就像以前在马铃薯VDAC中所观察到的那样。使用实时定量PCR分析发现,PgVDAC的转录表达谱在水杨酸(SA)的盐度,干燥,冷和外源施用的反应中被定量和动力学上调。然而,脱落酸(ABA)的外源应用对其表达没有影响。 PgVDAC的组成型过表达在转基因水稻植株中似乎有害。然而,低水平的上调赋予了盐分胁迫适应性响应。目前正在寻找更合适的诱导型转基因系统,以了解植物发育中的PgVDAC表达水平及其在逆境适应中的作用。 (c)2006年Elsevier Masson SAS。版权所有。

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