Green Kirsten A, Prigge Michael J, Katzman Rebecca B, Clark Steven E
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109-1048, USA.
Plant Cell. 2005 Mar;17(3):691-704. doi: 10.1105/tpc.104.026179. Epub 2005 Feb 10.
Organogenesis at the shoot meristem requires a delicate balance between stem cell specification and differentiation. In Arabidopsis thaliana, WUSCHEL (WUS) is a key factor promoting stem cell identity, whereas the CLAVATA (CLV1, CLV2, and CLV3) loci appear to promote differentiation by repressing WUS expression. In a screen for mutations modifying clv1 mutants, we have identified a novel regulator of meristem development we term CORONA (CNA). Whereas cna single mutant plants exhibit subtle defects in meristem development, clv cna double mutants develop massively enlarged apices that display early loss of organogenesis, misexpression of WUS and CLV3, and eventual differentiation of the entire apex. The CNA gene was isolated by positional cloning and found to encode a class III homeodomain Leu zipper protein. A missense mutation resulting in the dominant-negative cna-1 allele was identified in a conserved domain of unknown function, and a likely null allele was shown to display a similar but weaker phenotype. CNA is expressed in developing vascular tissue, diffusely through shoot and flower meristems, and within developing stamens and carpels. Our analysis of WUS expression in wild-type, clv, and clv cna plants revealed that, contrary to current models, WUS is neither necessary nor sufficient for stem cell specification and that neither WUS nor CLV3 is a marker for stem cell identity. We propose that CNA functions in parallel to the CLV loci to promote organ formation.
茎尖分生组织的器官发生需要干细胞特化与分化之间的微妙平衡。在拟南芥中,WUSCHEL(WUS)是促进干细胞特性的关键因子,而CLAVATA(CLV1、CLV2和CLV3)位点似乎通过抑制WUS表达来促进分化。在筛选修饰clv1突变体的突变时,我们鉴定出了一种新的分生组织发育调节因子,我们将其命名为CORONA(CNA)。虽然cna单突变体植株在分生组织发育中表现出细微缺陷,但clv cna双突变体发育出大量增大的顶端,表现出器官发生早期丧失、WUS和CLV3表达错误,以及整个顶端最终分化。通过图位克隆分离出CNA基因,发现其编码一个III类同源异型域亮氨酸拉链蛋白。在一个功能未知的保守结构域中鉴定出一个导致显性负性cna-1等位基因的错义突变,并且一个可能的无效等位基因表现出相似但较弱的表型。CNA在发育中的维管组织、通过茎尖和花分生组织广泛表达,以及在发育中的雄蕊和心皮中表达。我们对野生型、clv和clv cna植株中WUS表达的分析表明,与当前模型相反,WUS对于干细胞特化既不是必需的也不是充分的,并且WUS和CLV3都不是干细胞特性的标记。我们提出CNA与CLV位点平行发挥作用以促进器官形成。