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首页> 外文期刊>Journal of Experimental Botany >LATERAL ROOT PRIMORDIA 1 of maize acts as a transcriptional activator in auxin signalling downstream of the Aux/IAA gene rootless with undetectable meristem 1
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LATERAL ROOT PRIMORDIA 1 of maize acts as a transcriptional activator in auxin signalling downstream of the Aux/IAA gene rootless with undetectable meristem 1

机译:玉米的侧根原基1用作呼篷/ IAA基因无根的植物素信号传递激活剂,无可检测到未检测到的单位1

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Only little is known about target genes of auxin signalling downstream of the Aux/IAA-ARF module. In the present study, it has been demonstrated that maize lateral root primordia 1 (lrp1) encodes a transcriptional activator that is directly regulated by the Aux/IAA protein ROOTLESS WITH UNDETECTABLE MERISTEM 1 (RUM1). Expression of lrp1 is confined to early root primordia and meristems and is auxin-inducible. Based on its primary protein structure, LRP1 is predicted to be a transcription factor. This notion is supported by exclusive LRP1 localization in the nucleus and its ability to activate downstream gene activity. Based on the observation that lrp1 transcription is completely repressed in the semi-dominant gain of function mutant rum1, it was demonstrated that the lrp1 promoter is a direct target of RUM1 proteins. Subsequently, promoter activation assays indicated that RUM1 represses the expression of a GFP reporter fused to the native promoter of lrp1. Constitutive repression of lrp1 in rum1 mutants is a consequence of the stability of mutated rum1 proteins which cannot be degraded by the proteasome and thus constitutively bind to the lrp1 promoter and repress transcription. Taken together, the repression of the transcriptional activator lrp1 by direct binding of RUM1 to its promoter, together with specific expression of lrp1 in root meristems, suggests a function in maize root development via the RUM1-dependent auxin signalling pathway.
机译:关于AUXIN信号传导的毒素信号传导的靶基因仅熟知的是辅助/ IAA-ARF模块的靶基因。在本研究中,已经证明了玉米侧根原序1(LRP1)编码转录活化剂,其由无检测分类1(RuM1)直接由Aux / IAA蛋白无源调节。 LRP1的表达仅限于早期的根本原始和分生质,并且是一种诱导诱导的。基于其主要蛋白质结构,预测LRP1是转录因子。该概念由核中的独占LRP1本地化支持及其激活下游基因活性的能力。基于在功能突变突变体RuM1的半导体增益中完全抑制LRP1转录的观察结果,证明了LRP1启动子是RuM1蛋白的直接靶标。随后,启动子激活测定表明,RuM1抑制了与LRP1的天然启动子融合的GFP报告者的表达。在RuM1突变体中的LRP1的组成抑制是突变的RuM1蛋白的稳定性的结果,其不能通过蛋白酶降解并因此组成思考到LRP1启动子并抑制转录。连胜,通过直接结合RuM1至其启动子的转录活化剂LRP1抑制转录活化剂LRP1,以及RTP1在根转入中的特异性表达,并通过RuM1依赖性养肝信号传导途径在玉米根部发育中的功能。

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