Villarino Gonzalo H, Hu Qiwen, Manrique Silvia, Flores-Vergara Miguel, Sehra Bhupinder, Robles Linda, Brumos Javier, Stepanova Anna N, Colombo Lucia, Sundberg Eva, Heber Steffen, Franks Robert G
Department of Plant and Microbial Biology (G.H.V., M.F.-V., B.S., L.R., J.B., A.N.S., R.G.F.) and Department of Computer Science and Bioinformatics Research Center (Q.H., S.H.), North Carolina State University, Raleigh, North Carolina 27606;Università degli Studi di Milano Dip. di BioScienze, Sezione di Botanica Generale, Milan, Italy 20133 (S.M., L.C.); andDepartment of Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden 750 07 (E.S.).
Department of Plant and Microbial Biology (G.H.V., M.F.-V., B.S., L.R., J.B., A.N.S., R.G.F.) and Department of Computer Science and Bioinformatics Research Center (Q.H., S.H.), North Carolina State University, Raleigh, North Carolina 27606;Università degli Studi di Milano Dip. di BioScienze, Sezione di Botanica Generale, Milan, Italy 20133 (S.M., L.C.); andDepartment of Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden 750 07 (E.S.)
Plant Physiol. 2016 May;171(1):42-61. doi: 10.1104/pp.15.01845. Epub 2016 Mar 16.
Plant meristems, like animal stem cell niches, maintain a pool of multipotent, undifferentiated cells that divide and differentiate to give rise to organs. In Arabidopsis (Arabidopsis thaliana), the carpel margin meristem is a vital meristematic structure that generates ovules from the medial domain of the gynoecium, the female floral reproductive structure. The molecular mechanisms that specify this meristematic region and regulate its organogenic potential are poorly understood. Here, we present a novel approach to analyze the transcriptional signature of the medial domain of the Arabidopsis gynoecium, highlighting the developmental stages that immediately proceed ovule initiation, the earliest stages of seed development. Using a floral synchronization system and a SHATTERPROOF2 (SHP2) domain-specific reporter, paired with FACS and RNA sequencing, we assayed the transcriptome of the gynoecial medial domain with temporal and spatial precision. This analysis reveals a set of genes that are differentially expressed within the SHP2 expression domain, including genes that have been shown previously to function during the development of medial domain-derived structures, including the ovules, thus validating our approach. Global analyses of the transcriptomic data set indicate a similarity of the pSHP2-expressing cell population to previously characterized meristematic domains, further supporting the meristematic nature of this gynoecial tissue. Our method identifies additional genes including novel isoforms, cis-natural antisense transcripts, and a previously unrecognized member of the REPRODUCTIVE MERISTEM family of transcriptional regulators that are potential novel regulators of medial domain development. This data set provides genome-wide transcriptional insight into the development of the carpel margin meristem in Arabidopsis.
植物分生组织与动物干细胞微环境类似,维持着一群多能、未分化的细胞,这些细胞通过分裂和分化形成器官。在拟南芥中,心皮边缘分生组织是一种重要的分生组织结构,它从雌蕊(雌性花的生殖结构)的中间区域产生胚珠。然而,目前对于确定这个分生组织区域并调节其器官发生潜能的分子机制仍知之甚少。在这里,我们提出了一种新方法来分析拟南芥雌蕊中间区域的转录特征,突出了紧接胚珠起始之前的发育阶段,即种子发育的最早阶段。我们使用花同步系统和一个SHATTERPROOF2(SHP2)结构域特异性报告基因,结合荧光激活细胞分选(FACS)和RNA测序,以时空精确性分析了雌蕊中间区域的转录组。该分析揭示了一组在SHP2表达域内差异表达的基因,包括先前已证明在中间区域衍生结构(包括胚珠)发育过程中发挥作用的基因,从而验证了我们的方法。对转录组数据集的全局分析表明,表达pSHP2的细胞群体与先前鉴定的分生组织区域相似,进一步支持了这种雌蕊组织的分生组织性质。我们的方法鉴定出了其他基因,包括新的异构体、顺式天然反义转录本,以及转录调节因子生殖分生组织家族中一个先前未被识别的成员,它们可能是中间区域发育的潜在新调节因子。这个数据集提供了对拟南芥心皮边缘分生组织发育的全基因组转录见解。