Gu Fangwei, Bringmann Martin, Combs Jonathon R, Yang Jiyuan, Bergmann Dominique C, Nielsen Erik
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109-1048.
Department of Biology, Stanford University, Stanford, California 94305-5020.
Plant Cell. 2016 Jul;28(7):1722-37. doi: 10.1105/tpc.16.00203. Epub 2016 Jun 27.
In plants, the presence of a load-bearing cell wall presents unique challenges during cell division. Unlike other eukaryotes, which undergo contractile cytokinesis upon completion of mitosis, plants instead synthesize and assemble a new dividing cell wall to separate newly formed daughter cells. Here, we mine transcriptome data from individual cell types in the Arabidopsis thaliana stomatal lineage and identify CSLD5, a member of the Cellulose Synthase Like-D family, as a cell wall biosynthesis enzyme uniquely enriched in rapidly dividing cell populations. We further show that CSLD5 is a direct target of SPEECHLESS, the master transcriptional regulator of these divisions during stomatal development. Using a combination of genetic analysis and in vivo localization of fluorescently tagged fusion proteins, we show that CSLD5 preferentially accumulates in dividing plant cells where it participates in the construction of newly forming cell plates. We show that CSLD5 is an unstable protein that is rapidly degraded upon completion of cell division and that the protein turnover characteristics of CSLD5 are altered in ccs52a2 mutants, indicating that CSLD5 turnover may be regulated by a cell cycle-associated E3-ubiquitin ligase, the anaphase-promoting complex.
在植物中,承重细胞壁的存在给细胞分裂带来了独特的挑战。与其他真核生物不同,后者在有丝分裂完成后进行收缩性胞质分裂,而植物则合成并组装新的分裂细胞壁以分离新形成的子细胞。在这里,我们挖掘了拟南芥气孔谱系中单个细胞类型的转录组数据,并鉴定出纤维素合酶样D家族成员CSLD5,它是一种细胞壁生物合成酶,在快速分裂的细胞群体中特异性富集。我们进一步表明,CSLD5是气孔发育过程中这些分裂的主要转录调节因子无口(SPEECHLESS)的直接靶标。通过遗传分析和荧光标记融合蛋白的体内定位相结合,我们表明CSLD5优先积累在分裂的植物细胞中,在那里它参与新形成的细胞板的构建。我们表明CSLD5是一种不稳定蛋白,在细胞分裂完成后迅速降解,并且CSLD5的蛋白质周转特性在ccs52a2突变体中发生改变,这表明CSLD5的周转可能受细胞周期相关的E3泛素连接酶后期促进复合体调控。