Pautler Michael, Eveland Andrea L, LaRue Therese, Yang Fang, Weeks Rebecca, Lunde China, Je Byoung Il, Meeley Robert, Komatsu Mai, Vollbrecht Erik, Sakai Hajime, Jackson David
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724.
Department of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa 50010.
Plant Cell. 2015 Jan;27(1):104-20. doi: 10.1105/tpc.114.132506. Epub 2015 Jan 23.
Plant architecture is dictated by precise control of meristematic activity. In the shoot, an imbalance in positive or negative maintenance signals can result in a fasciated or enlarged meristem phenotype. fasciated ear4 (fea4) is a semidwarfed mutant with fasciated ears and tassels as well as greatly enlarged vegetative and inflorescence meristems. We identified FEA4 as a bZIP transcription factor, orthologous to Arabidopsis thaliana PERIANTHIA. FEA4 was expressed in the peripheral zone of the vegetative shoot apical meristem and in the vasculature of immature leaves and conspicuously excluded from the stem cell niche at the tip of the shoot apical meristem and from incipient leaf primordia. Following the transition to reproductive fate, FEA4 was expressed throughout the entire inflorescence and floral meristems. Native expression of a functional YFP:FEA4 fusion recapitulated this pattern of expression. We used chromatin immunoprecipitation-sequencing to identify 4060 genes proximal to FEA4 binding sites, including ones that were potentially bound and modulated by FEA4 based on transcriptional changes in fea4 mutant ears. Our results suggest that FEA4 promotes differentiation in the meristem periphery by regulating auxin-based responses and genes associated with leaf differentiation and polarity, potentially in opposition to factors such as KNOTTED1 and WUSCHEL.
植物结构由分生组织活性的精确控制所决定。在茎尖,正向或负向维持信号的失衡会导致分生组织出现扁化或增大的表型。扁化穗4(fea4)是一个半矮化突变体,其穗和雄穗扁化,营养分生组织和花序分生组织也大幅增大。我们将FEA4鉴定为一种bZIP转录因子,与拟南芥的PERIANTHIA直系同源。FEA4在营养茎尖分生组织的外周区以及未成熟叶片的维管系统中表达,明显排除在茎尖分生组织顶端的干细胞龛和初始叶原基之外。在转变为生殖命运后,FEA4在整个花序和花分生组织中表达。功能性YFP:FEA4融合蛋白的天然表达重现了这种表达模式。我们使用染色质免疫沉淀测序来鉴定FEA4结合位点附近的4060个基因,包括基于fea4突变穗中的转录变化而可能被FEA4结合和调控的基因。我们的结果表明,FEA4通过调节基于生长素的反应以及与叶分化和极性相关的基因,促进分生组织外周的分化,这可能与诸如KNOTTED1和WUSCHEL等因子相反。