Suppr超能文献

中介激酶模块的 CDK8 通过调节转录因子 SPEECHLESS(SPCH)的水平将叶片发育与正确的气孔模式建立联系。

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).

机构信息

Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, Umea, Sweden.

Department of Medical Biochemistry and Biophysics, Umeå University, Umea, Sweden.

出版信息

Plant Cell Environ. 2024 Dec;47(12):5237-5251. doi: 10.1111/pce.15102. Epub 2024 Aug 23.

Abstract

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 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 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 concentrations, as the accumulated levels of SPCH caused by the lack of CDK8 appear to override the negative regulation of increased CO. Thus, our work provides novel mechanistic understanding of how plants alter critical leaf properties in response to increasing atmospheric CO.

摘要

介体激酶模块的组成部分在所有真核生物谱系中高度保守,细胞周期蛋白依赖性激酶 8(CDK8)对于不同真核生物系统中正确的细胞增殖和分化是必不可少的。我们表明,CDK8 将叶片发育与正确的气孔模式建立联系起来,以适应 CO 条件。在拟南芥中,碱性螺旋-环-螺旋(bHLH)转录因子 SPEECHLESS(SPCH)控制细胞进入气孔细胞谱系,CDK8 与 SPCH 相互作用并磷酸化 SPCH,控制 SPCH 蛋白水平,从而也控制 SPCH 靶基因的表达,这些基因编码细胞命运和不对称细胞分裂的关键调节剂。缺乏 CDK8 介导的 SPCH 控制会导致分生组织母细胞和保卫母细胞数量增加,以及 cdk8 突变体中的气孔指数增加。大气 CO 浓度的增加会触发一个发育程序,通过限制不对称分裂来控制细胞进入气孔谱系。在 cdk8 中,在环境和高 CO 浓度下,分生组织母细胞和保卫母细胞的数量保持不变,因为缺乏 CDK8 导致的 SPCH 积累水平似乎超过了增加 CO 的负调节。因此,我们的工作提供了关于植物如何响应大气 CO 增加改变关键叶片特性的新的机制理解。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验