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MlWRKY12,一个新的芒转录因子,参与髓部次生细胞壁形成并促进开花。

MlWRKY12, a novel Miscanthus transcription factor, participates in pith secondary cell wall formation and promotes flowering.

机构信息

Key Laboratory of Biofuels, Chinese Academy of Sciences, Qingdao Institute of BioEnergy and Bioprocess Technology, Chinese Academy of Sciences (QIBEBT-CAS), Qingdao, Shandong, China.

出版信息

Plant Sci. 2013 Nov;212:1-9. doi: 10.1016/j.plantsci.2013.07.010. Epub 2013 Jul 29.

DOI:10.1016/j.plantsci.2013.07.010
PMID:24094048
Abstract

WRKY proteins play crucial roles in various plant processes. An AtWRKY12 homologous gene, named MlWRKY12, was isolated from Miscanthus lutarioriparius. The MlWRKY12 gene encodes a WRKY transcription factor belonging to the group IIc subfamily. MlWRKY12 is a nuclear protein. Gene expression pattern analysis revealed a relatively high MlWRKY12 expression level in rhizomes, stems and leaf sheaths. In situ hybridization analysis further demonstrated that MlWRKY12 was expressed in vascular bundle sheath, sclerenchyma and parenchyma tissues. The heterologous expression of MlWRKY12 in an atwrky12 background mutant successfully rescued the phenotype of pith cell walls caused by the defect of AtWRKY12. Most strikingly, the transgenic Arabidopsis plants overexpressing MlWRKY12 exhibited early flowering. The transcript abundance of flowering related genes was measured by quantitative RT-PCR analysis, suggesting that overexpression of MlWRKY12 in Arabidopsis had a significant impact on the expression level of CONSTANS (CO). Moreover, the expression levels of FLOWERING LOCUS T (FT), LFY (LEAFY), APETALA1 (AP1), CAULIFLOWER (CAL) and FRUITFULL (FUL) were upregulated in transgenic plants. These results demonstrated the conserved function of MlWRKY12 existing in secondary cell wall formation of monocotyledonous species and implied a possible impact of MlWRKY12 on flowering control.

摘要

WRKY 蛋白在各种植物过程中发挥着关键作用。从荻中分离到一个 AtWRKY12 同源基因,命名为 MlWRKY12。该基因编码一个属于 IIc 亚家族的 WRKY 转录因子。MlWRKY12 是一种核蛋白。基因表达模式分析显示,MlWRKY12 在根茎、茎和叶鞘中表达水平较高。原位杂交分析进一步表明,MlWRKY12 在维管束鞘、厚壁组织和薄壁组织中表达。在 atwrky12 背景突变体中异源表达 MlWRKY12 成功挽救了 AtWRKY12 缺陷导致的髓细胞壁的表型。最引人注目的是,过表达 MlWRKY12 的转基因拟南芥植物表现出早花。通过定量 RT-PCR 分析测量开花相关基因的转录丰度,表明 MlWRKY12 在拟南芥中的过表达对 CONSTANS (CO) 的表达水平有显著影响。此外,FT、LFY、AP1、CAL 和 FUL 的表达水平在转基因植物中上调。这些结果表明 MlWRKY12 在单子叶植物次生细胞壁形成中具有保守功能,并暗示 MlWRKY12 可能对开花调控有影响。

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