Publications des scientifiques de l'IRD

Ikeda Y., Nishihama R., Yamaoka S., Arteaga-Vazquez M. A., Aguilar-Cruz A., Grimanelli Daniel, Pogorelcnik R., Martienssen R. A., Yamato K. T., Kohchi T., Hirayama T., Mathieu O. (2018). Loss of CG methylation in Marchantia polymorpha causes disorganization of cell division and reveals unique DNA methylation regulatory mechanisms of non-CG methylation. Plant and Cell Physiology, 59 (12), p. 2421-2431. ISSN 0032-0781.

Titre du document
Loss of CG methylation in Marchantia polymorpha causes disorganization of cell division and reveals unique DNA methylation regulatory mechanisms of non-CG methylation
Année de publication
2018
Type de document
Article référencé dans le Web of Science WOS:000457606700004
Auteurs
Ikeda Y., Nishihama R., Yamaoka S., Arteaga-Vazquez M. A., Aguilar-Cruz A., Grimanelli Daniel, Pogorelcnik R., Martienssen R. A., Yamato K. T., Kohchi T., Hirayama T., Mathieu O.
Source
Plant and Cell Physiology, 2018, 59 (12), p. 2421-2431 ISSN 0032-0781
DNA methylation is an epigenetic mark that ensures silencing of transposable elements (TEs) and affects gene expression in many organisms. The function of different DNA methylation regulatory pathways has been largely characterized in the model plant Arabidopsis thaliana. However, far less is known about DNA methylation regulation and functions in basal land plants. Here we focus on the liverwort Marchantia polymorpha, an emerging model species that represents a basal lineage of land plants. We identified MpMET, the M. polymorpha ortholog of the METHYLTRANSFERASE 1 (MET1) gene required for maintenance of methylation at CG sites in angiosperms. We generated Mpmet mutants using the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/CRISPR-associated protein9) system, which showed a significant loss of CG methylation and severe morphological changes and developmental defects. The mutants developed many adventitious shoot-like structures, suggesting that MpMET is required for maintaining differentiated cellular identities in the gametophyte. Even though numerous TEs were up-regulated, nonCG methylation was generally highly increased at TEs in the Mpmet mutants. Closer inspection of CHG methylation revealed features unique to M. polymorpha. Methylation of CCG sites in M. polymorpha does not depend on MET1, unlike in A. thaliana and Physcomitrella patens. Our results highlight the diversity of non-CG methylation regulatory mechanisms in plants.
Plan de classement
Sciences fondamentales / Techniques d'analyse et de recherche [020] ; Sciences du monde végétal [076]
Identifiant IRD
PAR00018851
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