MET1-Dependent DNA Methylation Represses Light Signaling and Influences Plant Regeneration in Arabidopsis .
Sangrea ShimHong Gil LeePil Joon SeoPublished in: Molecules and cells (2022)
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 wild-type 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, MET1-dependent 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.
Keyphrases
- genome wide
- dna methylation
- stem cells
- tyrosine kinase
- wild type
- copy number
- network analysis
- genome wide identification
- single cell
- transcription factor
- gene expression
- wound healing
- mesenchymal stem cells
- cell therapy
- oxidative stress
- cell wall
- signaling pathway
- single molecule
- cell death
- drug induced
- circulating tumor cells