Institute for Biology, Plant Cell and Molecular Biology, Humboldt-Universität zu Berlin, 10115, Berlin, Germany.
Nat Commun. 2018 Oct 31;9(1):4534. doi: 10.1038/s41467-018-06772-3.
Floral homeotic transcription factors (TFs) act in a combinatorial manner to specify the organ identities in the flower. However, the architecture and the function of the gene regulatory network (GRN) controlling floral organ specification is still poorly understood. In particular, the interconnections of homeotic TFs, microRNAs (miRNAs) and other factors controlling organ initiation and growth have not been studied systematically so far. Here, using a combination of genome-wide TF binding, mRNA and miRNA expression data, we reconstruct the dynamic GRN controlling floral meristem development and organ differentiation. We identify prevalent feed-forward loops (FFLs) mediated by floral homeotic TFs and miRNAs that regulate common targets. Experimental validation of a coherent FFL shows that petal size is controlled by the SEPALLATA3-regulated miR319/TCP4 module. We further show that combinatorial DNA-binding of homeotic factors and selected other TFs is predictive of organ-specific patterns of gene expression. Our results provide a valuable resource for studying molecular regulatory processes underlying floral organ specification in plants.
花的同源异形转录因子 (TFs) 以组合的方式作用,以指定花中的器官身份。然而,控制花器官特化的基因调控网络 (GRN) 的结构和功能仍然知之甚少。特别是,控制器官起始和生长的同源异形 TF、microRNAs (miRNAs) 和其他因子之间的相互联系迄今为止尚未系统研究。在这里,我们使用全基因组 TF 结合、mRNA 和 miRNA 表达数据的组合,重建控制花分生组织发育和器官分化的动态 GRN。我们确定了由花同源异形 TF 和 miRNA 介导的常见靶标调节的普遍前馈环 (FFL)。我们进一步表明,SEPALLATA3 调节的 miR319/TCP4 模块调控花瓣大小。我们还表明,同源异形因子和选定的其他 TF 的组合 DNA 结合可预测器官特异性基因表达模式。我们的研究结果为研究植物花器官特化的分子调控过程提供了有价值的资源。