TY - JOUR
T1 - Loss of cg methylation in marchantia polymorpha causes disorganization of cell division and reveals unique dna methylation regulatory mechanisms of non-cg methylation
AU - Ikeda, Yoko
AU - Nishihama, Ryuichi
AU - Yamaoka, Shohei
AU - Arteaga-Vazquez, Mario A.
AU - Aguilar-Cruz, Adolfo
AU - Grimanelli, Daniel
AU - Pogorelcnik, Romain
AU - Martienssen, Robert A.
AU - Yamato, Katsuyuki T.
AU - Kohchi, Takayuki
AU - Hirayama, Takashi
AU - Mathieu, Olivier
N1 - Publisher Copyright:
© The Author(s) 2018.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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/CRISPRassociated 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, non- CG 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.
AB - 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/CRISPRassociated 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, non- CG 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.
KW - DNA methylation
KW - DNA methyltransferase
KW - Marchantia polymorpha
KW - RNA-directed DNA methylation
KW - Transposable elements
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U2 - 10.1093/pcp/pcy161
DO - 10.1093/pcp/pcy161
M3 - Article
C2 - 30102384
AN - SCOPUS:85058611451
SN - 0032-0781
VL - 59
SP - 2421
EP - 2431
JO - Plant and Cell Physiology
JF - Plant and Cell Physiology
IS - 12
ER -