Liu Linchuan, Tong Hongning, Xiao Yunhua, Che Ronghui, Xu Fan, Hu Bin, Liang Chengzhen, Chu Jinfang, Li Jiayang, Chu Chengcai
State Key Laboratory of Plant Genomics and National Center for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
State Key Laboratory of Plant Genomics and National Center for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China
Proc Natl Acad Sci U S A. 2015 Sep 1;112(35):11102-7. doi: 10.1073/pnas.1512748112. Epub 2015 Aug 17.
Grain size is one of the key factors determining grain yield. However, it remains largely unknown how grain size is regulated by developmental signals. Here, we report the identification and characterization of a dominant mutant big grain1 (Bg1-D) that shows an extra-large grain phenotype from our rice T-DNA insertion population. Overexpression of BG1 leads to significantly increased grain size, and the severe lines exhibit obviously perturbed gravitropism. In addition, the mutant has increased sensitivities to both auxin and N-1-naphthylphthalamic acid, an auxin transport inhibitor, whereas knockdown of BG1 results in decreased sensitivities and smaller grains. Moreover, BG1 is specifically induced by auxin treatment, preferentially expresses in the vascular tissue of culms and young panicles, and encodes a novel membrane-localized protein, strongly suggesting its role in regulating auxin transport. Consistent with this finding, the mutant has increased auxin basipetal transport and altered auxin distribution, whereas the knockdown plants have decreased auxin transport. Manipulation of BG1 in both rice and Arabidopsis can enhance plant biomass, seed weight, and yield. Taking these data together, we identify a novel positive regulator of auxin response and transport in a crop plant and demonstrate its role in regulating grain size, thus illuminating a new strategy to improve plant productivity.
粒重是决定谷物产量的关键因素之一。然而,目前仍不清楚发育信号如何调控粒重。在此,我们报告了从水稻T-DNA插入群体中鉴定和表征的一个显性突变体大粒1(Bg1-D),该突变体表现出超大粒表型。BG1的过表达导致粒重显著增加,严重的株系表现出明显的向重力性紊乱。此外,该突变体对生长素和生长素运输抑制剂N-1-萘基邻苯二甲酸均表现出更高的敏感性,而敲低BG1则导致敏感性降低和籽粒变小。此外,BG1在生长素处理后被特异性诱导,优先在茎秆和幼穗的维管组织中表达,并编码一种新的膜定位蛋白,强烈表明其在调节生长素运输中的作用。与此发现一致,该突变体的生长素向基运输增加,生长素分布改变,而敲低植株的生长素运输减少。在水稻和拟南芥中对BG1进行调控均可提高植物生物量、种子重量和产量。综合这些数据,我们在一种作物中鉴定出一种新的生长素应答和运输的正调控因子,并证明了其在调节粒重中的作用,从而为提高作物生产力阐明了一种新策略。