首页> 外文期刊>Journal of Experimental Botany >Relationships of root conductivity and aquaporin gene expression in Pisum sativum: diurnal patterns and the response to HgCl2 and ABA.
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Relationships of root conductivity and aquaporin gene expression in Pisum sativum: diurnal patterns and the response to HgCl2 and ABA.

机译:豌豆根电导率与水通道蛋白基因表达的关系:昼夜模式以及对HgCl2和ABA的响应。

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摘要

Experiments were undertaken to test how aquaporins (AQPs) facilitate the uptake of water by roots of Pisum sativum. Changes in PsPIP2-1 gene expression and root hydraulic conductivity (Lpr) were measured in response to the time of day as well as treatment of the roots with a compound that reduced Lpr [i.e. mercuric chloride (HgCl2)] and one that was intended to increase Lpr [abscisic acid (ABA)]. There was a diurnal rhythm in PsPIP2-1 expression in lateral roots that was strongly correlated with diurnal changes in Lpr. Taproots also displayed a rhythm in PsPIP2-1 expression, but this was offset from that of Lpr. This suggested that changes in Lpr were mediated by changes in PsPIP2-1 mRNA transcript abundance. Reduction of Lpr by HgCl2 treatment was accompanied by an increase in PsPIP2-1 expression, implying that PsPIP2-1 expression may have increased to compensate for AQPs blocked by mercury. ABA usually increased Lpr, but changes in PsPIP2-1 were variable and the direction of the response was strongly dependent on the dose of ABA that was applied. Overall, the coincident rhythms in Lpr and PIP2 expression and response to AQP blockage are consistent with the hypothesis that Lpr changes are mediated, at least in part, by changes in PsPIP2-1 expression. Inconsistencies with ABA data may have been due to more complex interactions of ABA with AQP channels..
机译:进行了实验以测试水通道蛋白(AQPs)如何促进豌豆根(Pisum sativum)的根吸收水。测量PsPIP2-1基因表达和根部水力传导率(Lpr)的变化以响应一天中的时间以及用降低Lpr的化合物处理根部[氯化汞(HgCl2)]和旨在增加Lpr [脱落酸(ABA)]的氯化汞。侧根PsPIP2-1表达的昼夜节律与Lpr的昼夜变化密切相关。主根在PsPIP2-1表达中也显示出节律,但这与Lpr有所不同。这表明Lpr的变化是由PsPIP2-1 mRNA转录物丰度的变化介导的。通过HgCl2处理降低的Lpr伴随着PsPIP2-1表达的增加,这意味着PsPIP2-1表达可能已经增加以补偿被汞阻断的AQP。 ABA通常会增加Lpr,但PsPIP2-1的变化是可变的,反应的方向强烈取决于所用ABA的剂量。总体而言,Lpr和PIP2表达的重合节奏以及对AQP阻滞的反应与Lpr改变至少部分地由PsPIP2-1表达的改变介导的假说是一致的。与ABA数据的不一致可能是由于ABA与AQP通道的相互作用更为复杂。

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