Ko Swee-Suak, Li Min-Jeng, Sun-Ben Ku Maurice, Ho Yi-Cheng, Lin Yi-Jyun, Chuang Ming-Hsing, Hsing Hong-Xian, Lien Yi-Chen, Yang Hui-Ting, Chang Hung-Chia, Chan Ming-Tsair
Academia Sinica Biotechnology Center in Southern Taiwan, Tainan 741, Taiwan Agricultural Biotechnology Research Center, Academia Sinica, Taipei 115, Taiwan
Academia Sinica Biotechnology Center in Southern Taiwan, Tainan 741, Taiwan.
Plant Cell. 2014 Jun;26(6):2486-2504. doi: 10.1105/tpc.114.126292. Epub 2014 Jun 3.
Male sterility plays an important role in F1 hybrid seed production. We identified a male-sterile rice (Oryza sativa) mutant with impaired pollen development and a single T-DNA insertion in the transcription factor gene bHLH142. Knockout mutants of bHLH142 exhibited retarded meiosis and defects in tapetal programmed cell death. RT-PCR and in situ hybridization analyses showed that bHLH142 is specifically expressed in the anther, in the tapetum, and in meiocytes during early meiosis. Three basic helix-loop-helix transcription factors, UDT1 (bHLH164), TDR1 (bHLH5), and EAT1/DTD1 (bHLH141) are known to function in rice pollen development. bHLH142 acts downstream of UDT1 and GAMYB but upstream of TDR1 and EAT1 in pollen development. In vivo and in vitro assays demonstrated that bHLH142 and TDR1 proteins interact. Transient promoter assays demonstrated that regulation of the EAT1 promoter requires bHLH142 and TDR1. Consistent with these results, 3D protein structure modeling predicted that bHLH142 and TDR1 form a heterodimer to bind to the EAT1 promoter. EAT1 positively regulates the expression of AP37 and AP25, which induce tapetal programmed cell death. Thus, in this study, we identified bHLH142 as having a pivotal role in tapetal programmed cell death and pollen development.
雄性不育在杂交水稻种子生产中发挥着重要作用。我们鉴定出一个花粉发育受损的雄性不育水稻(Oryza sativa)突变体,其转录因子基因bHLH142中存在单个T-DNA插入。bHLH142的敲除突变体表现出减数分裂延迟和绒毡层程序性细胞死亡缺陷。RT-PCR和原位杂交分析表明,bHLH142在花药、绒毡层以及减数分裂早期的减数分裂细胞中特异性表达。已知三个基本的螺旋-环-螺旋转录因子UDT1(bHLH164)、TDR1(bHLH5)和EAT1/DTD1(bHLH141)在水稻花粉发育中起作用。在花粉发育过程中,bHLH142在UDT1和GAMYB的下游起作用,但在TDR1和EAT1的上游起作用。体内和体外试验表明,bHLH142和TDR1蛋白相互作用。瞬时启动子试验表明,EAT1启动子的调控需要bHLH142和TDR1。与这些结果一致,三维蛋白质结构建模预测bHLH142和TDR1形成异源二聚体以结合EAT1启动子。EAT1正向调节AP37和AP25的表达,这两者可诱导绒毡层程序性细胞死亡。因此,在本研究中,我们鉴定出bHLH142在绒毡层程序性细胞死亡和花粉发育中起关键作用。