PdGNC confers drought tolerance by mediating stomatal closure resulting from NO and H2 O2 production via the direct regulation of PdHXK1 expression in Populus.
Chao ShenYue ZhangQing LiShujing LiuFang HeYi AnYangyan ZhouChao LiuWei-Lun YinXin-Li XiaPublished in: The New phytologist (2021)
Drought is one of the primary abiotic stresses, seriously implicating plant growth and productivity. Stomata play a crucial role in regulating drought tolerance. However, the molecular mechanism on stomatal movement-mediated drought tolerance remains unclear. Using genetic, molecular and biochemical techniques, we identified that the PdGNC directly activating the promoter of PdHXK1 by binding the GATC element, a hexokinase (HXK) synthesis key gene. Here, PdGNC, a member of the GATA transcription factor family, was greatly induced by abscisic acid and dehydration. Overexpressing PdGNC in poplar (Populus clone 717) resulted in reduced stomatal aperture with greater water-use efficiency and increased water deficit tolerance. By contrast, CRISPR/Cas9-mediated poplar mutant gnc exhibited increased stomatal aperture and water loss with reducing drought resistance. PdGNC activates PdHXK1 (a hexokinase synthesis key gene), resulting in a remarkable increase in hexokinase activity in poplars subjected to water deficit. Furthermore, hexokinase promoted nitric oxide (NO) and hydrogen peroxide (H2 O2 ) production in guard cells, which ultimately reduced stomatal aperture and increased drought resistance. Together, PdGNC confers drought stress tolerance by reducing stomatal aperture caused by NO and H2 O2 production via the direct regulation of PdHXK1 expression in poplars.
Keyphrases
- plant growth
- climate change
- hydrogen peroxide
- arabidopsis thaliana
- transcription factor
- nitric oxide
- heat stress
- crispr cas
- poor prognosis
- genome wide
- genome wide identification
- copy number
- signaling pathway
- gene expression
- induced apoptosis
- binding protein
- dna methylation
- genome editing
- magnetic resonance
- computed tomography
- cell death
- magnetic resonance imaging
- dna binding
- oxidative stress
- nitric oxide synthase
- cell proliferation