Cytosine methylation of the FWA promoter promotes direct in vitro shoot regeneration in Arabidopsis thaliana
Cytosine methylation of the FWA promoter promotes direct in vitro shoot regeneration in Arabidopsis thaliana
复制标题
FWA启动子的胞嘧啶甲基化促进拟南芥体外芽的直接再生
DOI:
10.1111/jipb.13156
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发表时间:
2021
影响因子:
11.4
通讯作者:
Xiang Fengning
中科院分区:
文献类型:
--
作者:
Dai Xuehuan;Wang Jing;Song Yuguang;Liu Zhenhua;Xue Tao;Qiao Meng;Yu Yanchong;Xin Wei;Xiang Fengning
Epigenetic modifications within promoter sequences can act as regulators of gene expression. Shoot regeneration is influenced by both DNA methylation and histone methylation, but the mechanistic basis of this regulation is obscure. Here, we identified 218 genes related to the regeneration capacity of callus that were differentially transcribed between regenerable calli (RC) and nonregenerable calli (NRC) in Arabidopsis thaliana. An analysis of the promoters of five of the differentially expressed genes (FWA, ACC1, TFL1, MAX3, and GRP3) pointed to an inverse relationship between cytosine methylation and transcription. The FWA promoter was demethylated and highly expressed in NRC, whereas it was methylated and expressed at low levels in RC. Explants of the hypomethylation mutants fwa-1 and fwa-2 showed strong levels of FWA expression and regenerated less readily than the wild type, suggesting that FWA inhibits direct in vitro shoot regeneration. WUSCHEL-RELATED HOMEOBOX 9 (WOX9), which is required for shoot apical meristem formation, was directly repressed by FWA. Overexpressing WOX9 partly rescued the shoot regeneration defect of fwa-2 plants. These findings suggest that cytosine methylation of the FWA promoter forms part of the regulatory system governing callus regenerability and direct in vitro shoot regeneration.