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首页> 外文期刊>Plant and Cell Physiology >Genetic Interactions Between Leaf Polarity-Controlling Genes and ASYMMETRIC LEAVES1 and 2 in Arabidopsis Leaf Patterning
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Genetic Interactions Between Leaf Polarity-Controlling Genes and ASYMMETRIC LEAVES1 and 2 in Arabidopsis Leaf Patterning

机译:拟南芥叶片模式中叶片极性控制基因与不对称叶1和2之间的遗传相互作用。

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During leaf development, establishment of adaxial–abaxial polarity is essential for normal leaf morphogenesis. This process is known to be strictly regulated by several putative transcription factors, microRNA165/166 (miR165/166), a trans-acting short-interfering RNA (tasiR-ARF), as well as proteins involved in RNA silencing. Among the putative transcription factor genes, ASYMMETRIC LEAVES1 and 2 (AS1 and 2) facilitate the specification of leaf adaxial identity; however, the mechanism by which AS1 and AS2 cooperate with other leaf polarity components remains largely undetermined. In the current study, we characterized the phenotype of mutants by combining as1 and as2 with mutations of several key transcription factors. Our data showed that double mutant plants carrying as1/as2 and rev, phb or phv enhanced as1/as2 defects by producing more severely abaxialized leaves. In contrast, triple mutants, obtained by combining as1/as2 with double mutant filamentous flower yabby3 (fil yab3) or kanadi1 kanadi2 (kan1 kan2), exhibited additive phenotypes. Additionally, while leaves of rev as2 contained high levels of FIL transcripts, only slightly elevated miR165/166 levels were noted, indicating that FIL and miR165/166 act in parallel in leaf patterning. Moreover, 35S::MIR165a/rev as2 transgenic plants resulted in a more severe abaxialized leaf phenotype than the rev and as2 single mutant plants transformed with the same 35S::MIR165a fusion. Genetic interactions between the key regulators during leaf patterning are discussed.
机译:在叶片发育过程中,建立正反极性对正常叶片形态发生至关重要。已知此过程受几种假定的转录因子,microRNA165 / 166(miR165 / 166),反式作用短干扰RNA(tasiR-ARF)以及参与RNA沉默的蛋白质的严格调控。在推定的转录因子基因中,ASYMMETRIC LEAVES1和2(AS1和2)促进了叶片近轴同一性的规范。但是,AS1和AS2与其他叶片极性组件协作的机制仍未确定。在当前的研究中,我们通过结合as1和as2与几个关键转录因子的突变来表征突变体的表型。我们的数据表明,携带as1 / as2和rev,phb或phv的双重突变植物通过产生更严重的背面化叶片来增强as1 / as2缺陷。相反,通过将as1 / as2与双重突变丝状花yabby3(fil yab3)或kanadi1 kanadi2(kan1 kan2)组合而获得的三重突变体表现出加性表型。此外,虽然rev as2的叶片中含有高水平的FIL转录本,但仅注意到miR165 / 166的水平略有升高,表明FIL和miR165 / 166在叶片模式中平行起作用。而且,与用相同的35S :: MIR165a融合体转化的rev和as2单突变植物相比,转为35S :: MIR165a / rev的as2转基因植物产生了更严重的叶表型。讨论了叶片图案形成过程中关键调控因子之间的遗传相互作用。

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