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Multiple genes tissue specificity and expression-dependent modulationcontribute to the functional diversity of potassium channels in Arabidopsis thaliana.

机译:多个基因组织特异性和依赖表达的调节有助于拟南芥钾通道的功能多样性。

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摘要

K+ channels play diverse roles in mediating K+ transport and in modulating the membrane potential in higher plant cells during growth and development. Some of the diversity in K+ channel functions may arise from the regulated expression of multiple genes encoding different K+ channel polypeptides. Here we report the isolation of a novel Arabidopsis thaliana cDNA (AKT2) that is highly homologous to the two previously identified K+ channel genes, KAT1 and AKT1. This cDNA mapped to the center of chromosome 4 by restriction fragment length polymorphism analysis and was highly expressed in leaves, whereas AKT1 was mainly expressed in roots. In addition, we show that diversity in K+ channel function may be attributable to differences in expression levels. Increasing KAT1 expression in Xenopus oocytes by polyadenylation of the KAT1 mRNA increased the current amplitude and led to higher levels of KAT1 protein, as assayed in western blots. The increase in KAT1 expression in oocytes produced shifts in the threshold potential for activation to more positive membrane potentials and decreased half-activation times. These results suggest that different levels of expression and tissue-specific expression of different K+ channel isoforms can contribute to the functional diversity of plant K+ channels. The identification of a highly expressed, leaf-specific K+ channel homolog in plants should allow further molecular characterization of K+ channel functions for physiological K+ transport processes in leaves.
机译:在生长和发育过程中,钾离子通道在介导钾离子转运和调节高等植物细胞膜电位方面发挥着多种作用。 K +通道功能的某些多样性可能源于编码不同K +通道多肽的多个基因的调控表达。在这里,我们报告了一个新的拟南芥cDNA(AKT2)的分离,该cDNA与先前确定的两个K +通道基因KAT1和AKT1高度同源。该cDNA通过限制性片段长度多态性分析定位到4号染色体的中心,并在叶中高表达,而AKT1主要在根中表达。此外,我们表明K +通道功能的多样性可能归因于表达水平的差异。通过Western印迹检测,通过KAT1 mRNA的多腺苷酸化作用,非洲爪蟾卵母细胞中KAT1表达的增加增加了电流幅度,并导致较高水平的KAT1蛋白。卵母细胞中KAT1表达的增加导致激活阈值电位向更正的膜电位转移,并减少了半激活时间。这些结果表明不同的K +通道同工型的不同表达水平和组织特异性表达可以促进植物K +通道的功能多样性。鉴定植物中高表达的叶特异性K +通道同源物应该可以进一步为叶子中的生理K +转运过程提供K +通道功能的分子表征。

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