Identification of Players Controlling Meristem Arrest Downstream of the FRUITFULL-APETALA2 Pathway.
Irene Martínez-FernándezStéfanie Menezes de MouraMarcio Alves-FerreiraCristina FerrándizVicente BalanzàPublished in: Plant physiology (2020)
The end of the reproductive phase in monocarpic plants is determined by a coordinated arrest of all active meristems, a process known as global proliferative arrest (GPA). GPA is linked to the correlative control exerted by developing seeds and, possibly, the establishment of strong source-sink relationships. It has been proposed that the meristems that undergo arrest at the end of the reproductive phase behave at the transcriptomic level as dormant meristems, with low mitotic activity and high expression of abscisic acid response genes. Meristem arrest is also controlled genetically. In Arabidopsis (Arabidopsis thaliana), the MADS-box transcription factor FRUITFULL induces GPA by directly repressing genes of the APETALA2 (AP2) clade. The AP2 genes maintain shoot apical meristem (SAM) activity in part by keeping WUSCHEL expression active, but the mechanisms downstream of this pathway remain elusive. To identify target genes, we performed a transcriptomic analysis, inducing AP2 activity in meristems close to arrest. Our results suggest that AP2 controls meristem arrest by repressing genes related to axillary bud dormancy in the SAM and negative regulators of cytokinin signaling. In addition, our analysis indicates that genes involved in the response to environmental signals also respond to AP2, suggesting that it could modulate the end of flowering by controlling responses to both endogenous and exogenous signals. Our results support the previous observation that at the end of the reproductive phase the arrested SAM behaves as a dormant meristem, and they strongly support AP2 as a master regulator of this process.
Keyphrases
- transcription factor
- genome wide identification
- cell cycle
- bioinformatics analysis
- dna binding
- genome wide
- arabidopsis thaliana
- poor prognosis
- squamous cell carcinoma
- genome wide analysis
- dna methylation
- binding protein
- risk assessment
- early stage
- radiation therapy
- lymph node
- single cell
- gene expression
- human health
- rectal cancer