Spatiotemporal regulation of cell-cycle genes by SHORTROOT links patterning and growth

生物 细胞周期 多细胞生物 细胞生物学 细胞分裂 染色质免疫沉淀 染色质 转录调控 电池类型 背景(考古学) 基因表达调控 细胞周期蛋白 转录因子 基因 细胞命运测定 基因表达 细胞 遗传学 细胞生长 发起人 古生物学
作者
Rosangela Sozzani,Hongchang Cui,Miguel Á. Moreno-Risueno,Wolfgang Busch,Jaimie Van Norman,Teva Vernoux,Siobhán M. Brady,Walter Dewitte,J. A. H. Murray,Philip N. Benfey
出处
期刊:Nature [Nature Portfolio]
卷期号:466 (7302): 128-132 被引量:424
标识
DOI:10.1038/nature09143
摘要

In higher animals and plants the processes of growth and patterning are coordinated. Much is known about the genes regulating patterning and many genes have been identified that are involved in cell-cycle control, but there are few instances in which a connection has been made between the two. A study of patterning in Arabidopsis root now shows that two key regulators of root-organ patterning directly control the transcription of specific components of the cell-cycle machinery. This demonstrates a direct link between developmental regulators, components of the cell-cycle machinery and organ patterning. In higher animals and plants, the processes of growth and patterning are coordinated. In this study, the authors study patterning in Arabidopsis root and show that two key regulators of root organ patterning directly control the transcription of specific components of the cell-cycle machinery. This study provides a direct link between developmental regulators, components of the cell-cycle machinery and organ patterning. The development of multicellular organisms relies on the coordinated control of cell divisions leading to proper patterning and growth1,2,3. The molecular mechanisms underlying pattern formation, particularly the regulation of formative cell divisions, remain poorly understood. In Arabidopsis, formative divisions generating the root ground tissue are controlled by SHORTROOT (SHR) and SCARECROW (SCR)4,5,6. Here we show, using cell-type-specific transcriptional effects of SHR and SCR combined with data from chromatin immunoprecipitation-based microarray experiments, that SHR regulates the spatiotemporal activation of specific genes involved in cell division. Coincident with the onset of a specific formative division, SHR and SCR directly activate a D-type cyclin; furthermore, altering the expression of this cyclin resulted in formative division defects. Our results indicate that proper pattern formation is achieved through transcriptional regulation of specific cell-cycle genes in a cell-type- and developmental-stage-specific context. Taken together, we provide evidence for a direct link between developmental regulators, specific components of the cell-cycle machinery and organ patterning.

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