Fiche publication


Date publication

juillet 2020

Journal

Plant physiology

Auteurs

Membres identifiés du Cancéropôle Est :
Mme COGNAT Valérie


Tous les auteurs :
Gentric N, Masoud K, Journot RP, Cognat V, Chabouté ME, Noir S, Genschik P

Résumé

In Arabidopsis (), the F-box protein F-BOX-LIKE17 (FBL17) was previously identified as an important cell-cycle regulatory protein. FBL17 is required for cell division during pollen development and for normal cell-cycle progression and endoreplication during the diploid sporophyte phase. FBL17 was reported to control the stability of the CYCLIN-DEPENDENT KINASE inhibitor KIP-RELATED PROTEIN (KRP), which may underlie the drastic reduction in cell division activity in both shoot and root apical meristems observed in loss-of-function mutants. However, whether FBL17 has other substrates and functions besides degrading KRPs remains poorly understood. Here we show that mutation of leads not only to misregulation of cell cycle genes, but also to a strong upregulation of genes involved in DNA damage and repair processes. This phenotype is associated with a higher frequency of DNA lesions in and increased cell death in the root meristem, even in the absence of genotoxic stress. Notably, the constitutive activation of DNA damage response genes is largely SOG1-independent in In addition, through analyses of root elongation, accumulation of cell death, and occurrence of γH2AX foci, we found that mutants are hypersensitive to DNA double-strand break-induced genotoxic stress. Notably, we observed that the FBL17 protein is recruited at nuclear foci upon double-strand break induction and colocalizes with γH2AX, but only in the presence of RETINOBLASTOMA RELATED1. Altogether, our results highlight a role for FBL17 in DNA damage response, likely by ubiquitylating proteins involved in DNA-damage signaling or repair.

Mots clés

Arabidopsis, drug effects, Arabidopsis Proteins, genetics, Bleomycin, pharmacology, Cell Nucleus, drug effects, DNA Breaks, Double-Stranded, drug effects, DNA Damage, DNA Repair, drug effects, DNA, Plant, metabolism, F-Box Proteins, metabolism, Gene Expression Regulation, Plant, drug effects, Mutation, genetics, Transcription Factors, metabolism, Transcriptome, genetics, Up-Regulation, drug effects

Référence

Plant Physiol. 2020 07;183(3):1295-1305