Lenhard Michael, Jürgens Gerd, Laux Thomas
Institut für Biologie III, Universität Freiburg, Schänzlestrasse 1, D-79104 Freiburg, Germany.
Development. 2002 Jul;129(13):3195-206. doi: 10.1242/dev.129.13.3195.
Continuous organ formation from the shoot apical meristem requires the integration of two functions: a set of undifferentiated, pluripotent stem cells is maintained at the very tip of the meristem, while their daughter cells in the periphery initiate organ primordia. The homeobox genes WUSCHEL (WUS) and SHOOTMERISTEMLESS (STM) encode two major regulators of meristem formation and maintenance in Arabidopsis, yet their interaction in meristem regulation is presently unclear. Here, we have addressed this question using loss- and gain-of-function approaches. We show that stem cell specification by WUS does not require STM activity. Conversely, STM suppresses differentiation independently of WUS and is required and sufficient to promote cell division. Consistent with their independent and distinct phenotypic effects, ectopic WUS and STM activities induce the expression of different downstream target genes. Finally, the pathways regulated by WUS and STM appear to converge in the suppression of differentiation, since coexpression of both genes produced a synergistic effect, and increased WUS activity could partly compensate for loss of STM function. These results suggest that WUS and STM share labour in the shoot apical meristem: WUS specifies a subset of cells in the centre as stem cells, while STM is required to suppress differentiation throughout the meristem dome, thus allowing stem cell daughters to be amplified before they are incorporated into organs.
一组未分化的多能干细胞维持在分生组织的最顶端,而其外周的子细胞启动器官原基的形成。同源异型盒基因WUSCHEL(WUS)和SHOOTMERISTEMLESS(STM)编码拟南芥中分生组织形成和维持的两个主要调节因子,然而它们在分生组织调控中的相互作用目前尚不清楚。在这里,我们使用功能缺失和功能获得方法解决了这个问题。我们表明,WUS对干细胞的特化不需要STM的活性。相反,STM独立于WUS抑制分化,并且是促进细胞分裂所必需且足够的。与其独立且不同的表型效应一致,异位的WUS和STM活性诱导不同下游靶基因的表达。最后,由WUS和STM调控的途径似乎在抑制分化方面汇聚,因为这两个基因的共表达产生了协同效应,并且增加的WUS活性可以部分补偿STM功能的丧失。这些结果表明,WUS和STM在茎尖分生组织中分工合作:WUS将中心的一部分细胞特化为干细胞,而STM则需要抑制整个分生组织圆顶的分化,从而使干细胞的子代在被纳入器官之前得以扩增。