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大豆miR172c靶向抑制性AP2转录因子NNC1,以激活ENOD40表达并调节根瘤起始。

Soybean miR172c targets the repressive AP2 transcription factor NNC1 to activate ENOD40 expression and regulate nodule initiation.

作者信息

Wang Youning, Wang Lixiang, Zou Yanmin, Chen Liang, Cai Zhaoming, Zhang Senlei, Zhao Fang, Tian Yinping, Jiang Qiong, Ferguson Brett J, Gresshoff Peter M, Li Xia

机构信息

Key State Laboratory of Plant Cell and Chromosome Engineering, Center of Agricultural Resources Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Shijiazhuang, Hebei 050021, China.

Key State Laboratory of Plant Cell and Chromosome Engineering, Center of Agricultural Resources Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Shijiazhuang, Hebei 050021, China University of the Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Plant Cell. 2014 Dec;26(12):4782-801. doi: 10.1105/tpc.114.131607. Epub 2014 Dec 30.

Abstract

MicroRNAs are noncoding RNAs that act as master regulators to modulate various biological processes by posttranscriptionally repressing their target genes. Repression of their target mRNA(s) can modulate signaling cascades and subsequent cellular events. Recently, a role for miR172 in soybean (Glycine max) nodulation has been described; however, the molecular mechanism through which miR172 acts to regulate nodulation has yet to be explored. Here, we demonstrate that soybean miR172c modulates both rhizobium infection and nodule organogenesis. miR172c was induced in soybean roots inoculated with either compatible Bradyrhizobium japonicum or lipooligosaccharide Nod factor and was highly upregulated during nodule development. Reduced activity and overexpression of miR172c caused dramatic changes in nodule initiation and nodule number. We show that soybean miR172c regulates nodule formation by repressing its target gene, Nodule Number Control1, which encodes a protein that directly targets the promoter of the early nodulin gene, ENOD40. Interestingly, transcriptional levels of miR172c were regulated by both Nod Factor Receptor1α/5α-mediated activation and by autoregulation of nodulation-mediated inhibition. Thus, we established a direct link between miR172c and the Nod factor signaling pathway in addition to adding a new layer to the precise nodulation regulation mechanism of soybean.

摘要

微小RNA是一类非编码RNA,作为主要调节因子,通过转录后抑制其靶基因来调节各种生物学过程。对其靶mRNA的抑制可调节信号级联反应及随后的细胞事件。最近,已有研究描述了miR172在大豆(Glycine max)结瘤中的作用;然而,miR172调节结瘤的分子机制尚待探索。在此,我们证明大豆miR172c可调节根瘤菌感染和根瘤器官发生。miR172c在接种了共生慢生根瘤菌或脂寡糖结瘤因子的大豆根中被诱导,并且在根瘤发育过程中高度上调。miR172c活性降低和过表达导致根瘤起始和根瘤数量发生显著变化。我们表明,大豆miR172c通过抑制其靶基因Nodule Number Control1来调节根瘤形成,该基因编码一种直接靶向早期结瘤素基因ENOD40启动子的蛋白质。有趣的是,miR172c的转录水平受结瘤因子受体1α/5α介导的激活以及结瘤自调节介导的抑制作用调控。因此,我们不仅在大豆精确的结瘤调节机制中增加了新的层次,还建立了miR172c与结瘤因子信号通路之间的直接联系。

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