首页> 外文期刊>Plant physiology >Banana Transcription Factor MaERF11 Recruits Histone Deacetylase MaHDA1 and Represses the Expression of MaACO1 and Expansins during Fruit Ripening
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Banana Transcription Factor MaERF11 Recruits Histone Deacetylase MaHDA1 and Represses the Expression of MaACO1 and Expansins during Fruit Ripening

机译:香蕉转录因子MaERF11募集组蛋白脱乙酰基酶MaHDA1,并抑制果实成熟期间MaACO1和expansins的表达

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摘要

Phytohormone ethylene controls diverse developmental and physiological processes such as fruit ripening via modulation of ethylene signaling pathway. Our previous study identified that ETHYLENE RESPONSE FACTOR11 (MaERF11), a transcription factor in the ethylene signaling pathway, negatively regulates the ripening of banana, but the mechanism for the MaERF11-mediated transcriptional regulation remains largely unknown. Here we showed that MaERF11 has intrinsic transcriptional repression activity in planta. Electrophoretic mobility shift assay and chromatin immunoprecipitation analyses demonstrated that MaERF11 binds to promoters of three ripening-related Expansin genes, MaEXP2, MaEXP7 and MaEXP8, as well as an ethylene biosynthetic gene MaACO1, via the GCC-box motif. Furthermore, expression patterns of MaACO1, MaEXP2, MaEXP7, and MaEXP8 genes are correlated with the changes of histone H3 and H4 acetylation level during fruit ripening. Moreover, we found that MaERF11 physically interacts with a histone deacetylase, MaHDA1, which has histone deacetylase activity, and the interaction significantly strengthens the MaERF11-mediated transcriptional repression of MaACO1 and Expansins. Taken together, these findings suggest that MaERF11 may recruit MaHDA1 to its target genes and repress their expression via histone deacetylation.
机译:植物激素乙烯通过调节乙烯信号传导途径控制多种发育和生理过程,例如果实成熟。我们之前的研究发现,乙烯信号传导途径中的转录因子“乙烯反应因子11”(MaERF11)负调控香蕉的成熟,但是在很大程度上,MaERF11介导的转录调控机制尚不清楚。在这里,我们证明了MaERF11在植物中具有固有的转录抑制活性。电泳迁移率迁移分析和染色质免疫沉淀分析表明,MaERF11通过GCC-box母题与三个成熟相关的Expansin基因MaEXP2,MaEXP7和MaEXP8的启动子以及乙烯生物合成基因MaACO1结合。此外,MaACO1,MaEXP2,MaEXP7和MaEXP8基因的表达模式与果实成熟过程中组蛋白H3和H4乙酰化水平的变化相关。此外,我们发现MaERF11与具有组蛋白脱乙酰基酶活性的组蛋白脱乙酰基酶MaHDA1物理相互作用,并且这种相互作用显着增强了MaERF11介导的MaACO1和Expansins的转录抑制。综上所述,这些发现表明MaERF11可能将MaHDA1募集到其靶基因,并通过组蛋白脱乙酰化抑制其表达。

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