CDK8 of the mediator kinase module connects leaf development to the establishment of correct stomata patterning by regulating the levels of the transcription factor SPEECHLESS (SPCH).
Carmen Hermida-CarreraAlexander VergaraLuis Cervela-CardonaXu JinStefan BjörklundÅsa StrandPublished in: Plant, cell & environment (2024)
The components of the mediator kinase module are highly conserved across all eukaryotic lineages, and cyclin-dependent kinase 8 (CDK8) is essential for correct cell proliferation and differentiation in diverse eukaryotic systems. We show that CDK8 couples leaf development with the establishment of correct stomata patterning for prevailing CO 2 conditions. In Arabidopsis, the basic helix-loop-helix (bHLH) transcription factor SPEECHLESS (SPCH) controls cellular entry into the stomatal cell lineage, and CDK8 interacts with and phosphorylates SPCH, controlling SPCH protein levels and thereby also expression of the SPCH target genes encoding key regulators of cell fate and asymmetric cell divisions. The lack of the CDK8-mediated control of SPCH results in an increased number of meristemoid and guard mother cells, and increased stomata index in the cdk8 mutants. Increasing atmospheric CO 2 concentrations trigger a developmental programme controlling cell entry into stomatal lineage by limiting the asymmetric divisions. In cdk8, the number of meristemoids and guard mother cells remains the same under ambient and high CO 2 concentrations, as the accumulated levels of SPCH caused by the lack of CDK8 appear to override the negative regulation of increased CO 2 . Thus, our work provides novel mechanistic understanding of how plants alter critical leaf properties in response to increasing atmospheric CO 2 .
Keyphrases
- cell cycle
- transcription factor
- cell proliferation
- cell fate
- single cell
- dna binding
- induced apoptosis
- cell cycle arrest
- particulate matter
- cell therapy
- poor prognosis
- randomized controlled trial
- binding protein
- clinical trial
- endoplasmic reticulum stress
- cell death
- bone marrow
- genome wide
- study protocol
- gene expression
- long non coding rna
- protein protein