生物
DNA甲基化
老茧
拟南芥
甲基化
遗传学
基因
细胞生物学
突变体
基因表达
作者
Sangrea Shim,Hong Gil Lee,Pil Joon Seo
出处
期刊:Molecules and Cells
[Springer Science+Business Media]
日期:2021-10-01
卷期号:44 (10): 746-757
被引量:15
标识
DOI:10.14348/molcells.2021.0160
摘要
Plant somatic cells can be reprogrammed into a pluripotent cell mass, called callus, which can be subsequently used for de novo shoot regeneration through a two-step in vitro tissue culture method.MET1-dependent CG methylation has been implicated in plant regeneration in Arabidopsis, because the met1-3 mutant exhibits increased shoot regeneration compared with the wild-type.To understand the role of MET1 in de novo shoot regeneration, we compared the genome-wide DNA methylomes and transcriptomes of wildtype and met1-3 callus and leaf.The CG methylation patterns were largely unchanged during leaf-to-callus transition, suggesting that the altered regeneration phenotype of met1-3 was caused by the constitutively hypomethylated genes, independent of the tissue type.In particular, MET1dependent CG methylation was observed at the blue light receptor genes, CRYPTOCHROME 1 (CRY1) and CRY2, which reduced their expression.Coexpression network analysis revealed that the CRY1 gene was closely linked to cytokinin signaling genes.Consistently, functional enrichment analysis of differentially expressed genes in met1-3 showed that gene ontology terms related to light and hormone signaling were overrepresented.Overall, our findings indicate that MET1-dependent repression of light and cytokinin signaling influences plant regeneration capacity and shoot identity establishment.
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