Yang Weibing, Schuster Christoph, Beahan Cherie T, Charoensawan Varodom, Peaucelle Alexis, Bacic Antony, Doblin Monika S, Wightman Raymond, Meyerowitz Elliot M
Sainsbury Laboratory, University of Cambridge, Bateman Street, Cambridge CB2 1LR, UK.
ARC Centre of Excellence in Plant Cell Walls, School of BioSciences, The University of Melbourne, Parkville, VIC 3010, Australia.
Curr Biol. 2016 Jun 6;26(11):1404-15. doi: 10.1016/j.cub.2016.04.026. Epub 2016 May 19.
The cell walls of the shoot apical meristem (SAM), containing the stem cell niche that gives rise to the above-ground tissues, are crucially involved in regulating differentiation. It is currently unknown how these walls are built and refined or their role, if any, in influencing meristem developmental dynamics. We have combined polysaccharide linkage analysis, immuno-labeling, and transcriptome profiling of the SAM to provide a spatiotemporal plan of the walls of this dynamic structure. We find that meristematic cells express only a core subset of 152 genes encoding cell wall glycosyltransferases (GTs). Systemic localization of all these GT mRNAs by in situ hybridization reveals members with either enrichment in or specificity to apical subdomains such as emerging flower primordia, and a large class with high expression in dividing cells. The highly localized and coordinated expression of GTs in the SAM suggests distinct wall properties of meristematic cells and specific differences between newly forming walls and their mature descendants. Functional analysis demonstrates that a subset of CSLD genes is essential for proper meristem maintenance, confirming the key role of walls in developmental pathways.
茎尖分生组织(SAM)的细胞壁包含产生地上组织的干细胞龛,在调节分化过程中起着至关重要的作用。目前尚不清楚这些细胞壁是如何构建和完善的,以及它们在影响分生组织发育动态方面是否有作用。我们结合了多糖连接分析、免疫标记和SAM的转录组分析,以提供这个动态结构细胞壁的时空图谱。我们发现,分生组织细胞仅表达152个编码细胞壁糖基转移酶(GTs)基因的核心子集。通过原位杂交对所有这些GT mRNA进行系统定位,揭示了在顶端亚域(如正在出现的花原基)富集或具有特异性的成员,以及在分裂细胞中高表达的一大类成员。GTs在SAM中的高度局部化和协调表达表明分生组织细胞具有独特的细胞壁特性,以及新形成的细胞壁与其成熟后代之间的特定差异。功能分析表明,CSLD基因的一个子集对于分生组织的正常维持至关重要,证实了细胞壁在发育途径中的关键作用。