Okada T, Sasaki Y, Ohta R, Onozuka N, Toriyama K
Laboratory of Plant Breeding and Genetics, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan.
Plant Cell Physiol. 2000 Jun;41(6):757-66. doi: 10.1093/pcp/41.6.757.
Bra r 1 encodes a Ca2+-binding protein specifically expressed in anthers of Brassica rapa. In this study, we isolated a genomic clone of Bra r 1 and found sequences similar to Pollen Box core motifs and LAT56/59 box, pollen-specific cis-acting element, in the 5' upstream region of Bra r 1. Reporter gene fusion revealed that the Bra r 1 promoter directs male gametophytic expression in Nicotiana tabacum, Arabidopsis thaliana and B. napus, showing strong expression in mature pollen grains similar to that of endogenous Bra r 1. Genomic DNA of Bra r 1 was introduced into tobacco plants and the highest accumulation of Bra r 1 protein was observed in mature pollen in the same manner as reporter gene expression. Using in vitro-germinated pollen tubes of transgenic tobacco, we firstly demonstrated the subcellular localization of Bra r 1 in pollen tubes. Bra r 1 protein was distributed throughout the pollen tube of transgenic tobacco and slightly intense signals of Bra r 1 were observed in the tip region. In long-germinated pollen tubes, Bra r 1 was detected only in the cytoplasmic compartments while no signals were observed in the empty part of the pollen tube, indicating that cytoplasmic movement toward the tube tip is accompanied by Bra r 1. Hence, we suggest that Bra r 1 is involved in pollen germination and pollen tube growth.
Bra r 1编码一种在甘蓝型油菜花药中特异性表达的钙结合蛋白。在本研究中,我们分离出Bra r 1的基因组克隆,并在Bra r 1的5'上游区域发现了与花粉盒核心基序和花粉特异性顺式作用元件LAT56/59盒相似的序列。报告基因融合显示,Bra r 1启动子在烟草、拟南芥和甘蓝型油菜中指导雄配子体表达,在成熟花粉粒中表现出与内源性Bra r 1相似的强表达。将Bra r 1的基因组DNA导入烟草植株,观察到Bra r 1蛋白在成熟花粉中的积累量最高,与报告基因表达情况相同。利用转基因烟草的体外萌发花粉管,我们首次证明了Bra r 1在花粉管中的亚细胞定位。Bra r 1蛋白分布于转基因烟草的整个花粉管中,在顶端区域观察到稍强的Bra r 1信号。在长萌发花粉管中,仅在细胞质区域检测到Bra r 1,而在花粉管的空部分未观察到信号,表明向管尖的细胞质运动伴随着Bra r 1。因此,我们认为Bra r 1参与花粉萌发和花粉管生长。