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玉米的侧根原基1在Aux/IAA基因无根且分生组织不可检测1下游的生长素信号传导中作为转录激活因子发挥作用。

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.

作者信息

Zhang Yanxiang, von Behrens Inga, Zimmermann Roman, Ludwig Yvonne, Hey Stefan, Hochholdinger Frank

机构信息

INRES, Institute of Crop Science and Resource Conservation, Crop Functional Genomics, Friedrich-Ebert-Allee 144, University of Bonn, D-53113 Bonn, Germany Center for Molecular Cell and Systems Biology, College of Life Science, Fujian Agriculture & Forestry University, 350002 Fuzhou, China.

ZMBP, Center for Plant Molecular Biology, Department of General Genetics, University of Tuebingen, D-72076 Tuebingen, Germany.

出版信息

J Exp Bot. 2015 Jul;66(13):3855-63. doi: 10.1093/jxb/erv187. Epub 2015 Apr 23.

Abstract

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.

摘要

关于生长素信号转导Aux/IAA-ARF模块下游的靶基因,人们了解甚少。在本研究中,已证明玉米侧根原基1(lrp1)编码一种转录激活因子,该因子受Aux/IAA蛋白无根且分生组织不可检测1(RUM1)直接调控。lrp1的表达局限于早期根原基和分生组织,且受生长素诱导。基于其蛋白质一级结构,预测LRP1为转录因子。LRP1仅定位于细胞核及其激活下游基因活性的能力支持了这一观点。基于在半显性功能获得突变体rum1中lrp1转录完全受抑制这一观察结果,证明lrp1启动子是RUM1蛋白的直接靶标。随后,启动子激活分析表明,RUM1抑制与lrp1天然启动子融合的GFP报告基因的表达。rum1突变体中lrp1的组成型抑制是突变的rum1蛋白稳定性的结果,这些蛋白不能被蛋白酶体降解,因此组成型结合到lrp1启动子并抑制转录。综上所述,RUM1直接结合其启动子对转录激活因子lrp1的抑制,以及lrp1在根分生组织中的特异性表达,表明其通过RUM1依赖的生长素信号通路在玉米根发育中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85d1/4473986/495380022806/exbotj_erv187_f0001.jpg

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