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LOFSEP 转录因子功能丧失导致水稻小穗转化为叶状结构。

Loss of LOFSEP Transcription Factor Function Converts Spikelet to Leaf-Like Structures in Rice.

机构信息

Joint International Research Laboratory of Metabolic and Developmental Sciences, State Key Laboratory of Hybrid Rice, Shanghai Jiao Tong University-University of Adelaide Joint Centre for Agriculture and Health, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.

Instituto de Biología Molecular y Celular de Plantas, Consejo Superior de Investigaciones Científicas-Universidad Politécnica de Valencia, Valencia 46022, Spain.

出版信息

Plant Physiol. 2018 Feb;176(2):1646-1664. doi: 10.1104/pp.17.00704. Epub 2017 Dec 7.

Abstract

()-like genes, which encode a subfamily of MADS-box transcription factors, are essential for specifying floral organ and meristem identity in angiosperms. Rice () has five -like genes with partial redundancy and overlapping expression domains, yet their functions and evolutionary conservation are only partially known. Here, we describe the biological role of one of the genes of rice, , in redundantly controlling spikelet morphogenesis. belongs to the conserved subgroup along with and was expressed strongly across a broad range of reproductive stages and tissues. No obvious phenotype was observed in the single mutants when compared with the wild type, which was largely due to the functional redundancy among the three genes. Genetic and molecular analyses demonstrated that , , and together regulate floral meristem determinacy and specify the identities of spikelet organs by positively regulating the other MADS-box floral homeotic genes. Experiments conducted in yeast also suggested that OsMADS1, OsMADS5, and OsMADS34 form protein-protein interactions with other MADS-box floral homeotic members, which seems to be a typical, conserved feature of plant SEP proteins.

摘要

类基因,编码 MADS-box 转录因子的一个亚家族,对于被子植物中花器官和分生组织的特化是必不可少的。水稻有五个类基因,具有部分冗余和重叠的表达域,但它们的功能和进化保守性仅部分已知。在这里,我们描述了水稻类基因之一的生物学功能,在冗余控制小穗形态发生中。属于保守的亚组,与和一起在广泛的生殖阶段和组织中强烈表达。与野生型相比,单突变体中没有观察到明显的表型,这主要是由于三个基因之间的功能冗余。遗传和分子分析表明,、和一起通过正向调控其他 MADS-box 花同源基因来调节花分生组织的确定性,并指定小穗器官的身份。酵母中的实验还表明,OsMADS1、OsMADS5 和 OsMADS34 与其他 MADS-box 花同源基因形成蛋白-蛋白相互作用,这似乎是植物 SEP 蛋白的一个典型、保守的特征。

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