4.7 Article

Integrated Methylome and Transcriptome Analyses Reveal the Molecular Mechanism by Which DNA Methylation Regulates Kenaf Flowering

Journal

FRONTIERS IN PLANT SCIENCE
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2021.709030

Keywords

kenaf (Hibiscus cannabinus L; ); DNA methylation; 5-azacytidine (5-azaC); flowering; transcriptome

Categories

Funding

  1. National Natural Science Foundation of China [31960368]
  2. earmarked fund for China Agriculture Research System of MOF and MARA [CARS-16-E14]

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This study revealed that pretreatment of kenaf seedlings with 200 μM 5-azaC effectively promoted flowering. Biochemical analysis showed significant alterations in plant hormone levels and starch metabolism, along with differential expression of numerous genes. Integrated genome-wide DNA methylation and transcriptome analyses identified genes involved in plant hormone signal transduction, starch and sucrose metabolism, and flowering regulation, potentially impacting early flowering processes.
DNA methylation regulates key biological processes in plants. In this study, kenaf seedlings were pretreated with the DNA methylation inhibitor 5-azacytidine (5-azaC) (at concentrations of 0, 100, 200, 400, and 600 mu M), and the results showed that pretreatment with 200 mu M 5-azaC promoted flowering most effectively. To elucidate the underlying mechanism, phytohormone, adenosine triphosphate (ATP), and starch contents were determined, and genome-wide DNA methylation and transcriptome analyses were performed on anthers pretreated with 200 mu M 5-azaC (5-azaC200) or with no 5-azaC (control conditions; 5-azaC0). Biochemical analysis revealed that 5-azaC pretreatment significantly reduced indoleacetic acid (IAA) and gibberellic acid (GA) contents and significantly increased abscisic acid (ABA) and ATP contents. The starch contents significantly increased in response to 200 and 600 mu M 5-azaC. Further genome-wide DNA methylation analysis revealed 451 differentially methylated genes (DMGs) with 209 up- and 242 downregulated genes. Transcriptome analysis showed 3,986 differentially expressed genes (DEGs), with 2,171 up- and 1,815 downregulated genes. Integrated genome-wide DNA methylation and transcriptome analyses revealed 72 genes that were both differentially methylated and differentially expressed. These genes, which included ARFs, PP2C, starch synthase, FLC, PIF1, AGL80, and WRKY32, are involved mainly in plant hormone signal transduction, starch and sucrose metabolism, and flowering regulation and may be involved in early flowering. This study serves as a reference and theoretical basis for kenaf production and provides insights into the effects of DNA methylation on plant growth and development.

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