Li Chengxia, Potuschak Thomas, Colón-Carmona Adán, Gutiérrez Rodrigo A, Doerner Peter
Institute for Molecular Plant Science, School of Biological Sciences, University of Edinburgh, EH9 3JR Edinburgh, Scotland.
Proc Natl Acad Sci U S A. 2005 Sep 6;102(36):12978-83. doi: 10.1073/pnas.0504039102. Epub 2005 Aug 25.
During postembryonic plant development, cell division is coupled to cell growth. There is a stringent requirement to couple these processes in shoot and root meristems. As cells pass through meristems, they transit through zones with high rates of cell growth and proliferation during organogenesis. This transition implies a need for coordinate regulation of genes underpinning these two fundamental cell functions. Here, we report a mechanism for coregulation of cell division control genes and cell growth effectors. We identified a GCCCR motif necessary and sufficient for high-level cyclin CYCB1;1 expression at G2/M. This motif is overrepresented in many ribosomal protein gene promoters and is required for high-level expression of the S27 and L24 ribosomal subunit genes we examined. p33(TCP20), encoded by the Arabidopsis TCP20 gene, binds to the GCCCR element in the promoters of cyclin CYCB1;1 and ribosomal protein genes in vitro and in vivo. We propose a model in which organ growth rates, and possibly shape in aerial organs, are regulated by the balance of positively and negatively acting teosinte-branched, cycloidea, PCNA factor (TCP) genes in the distal meristem boundary zone where cells become mitotically quiescent before expansion and differentiation.
在植物胚后发育过程中,细胞分裂与细胞生长相关联。在茎尖和根尖分生组织中,严格要求这两个过程相互协调。当细胞通过分生组织时,它们在器官发生过程中会经过细胞生长和增殖速率较高的区域。这种转变意味着需要对支撑这两种基本细胞功能的基因进行协调调控。在此,我们报道了一种细胞分裂控制基因和细胞生长效应因子共同调控的机制。我们鉴定出一个GCCCR基序,它对于细胞周期蛋白CYCB1;1在G2/M期的高水平表达是必需且充分的。这个基序在许多核糖体蛋白基因启动子中高度富集,并且是我们所检测的S27和L24核糖体亚基基因高水平表达所必需的。拟南芥TCP20基因编码的p33(TCP20)在体外和体内均能与细胞周期蛋白CYCB1;1和核糖体蛋白基因启动子中的GCCCR元件结合。我们提出了一个模型,即在远端分生组织边界区,细胞在扩展和分化之前进入有丝分裂静止期,器官生长速率以及可能地上器官的形状受正向和负向作用的玉米分枝、环化、增殖细胞核抗原因子(TCP)基因平衡的调控。