Park Beom Seok, Park Young Doo, Kim Hyun Uk, Jin Yong Moon, Kim Ho Il
Genomics Division, National Institute of Agricultural Biotechnology, Rural Development Administration, Suwon, Korea.
Mol Cells. 2002 Aug 31;14(1):150-7.
We isolated and characterized a pollen-preferential gene, BAN103, from Chinese cabbage and analyzed the activity of its promoter. The BAN103 cDNA and genomic clone that contained the full-length gene were sequenced. The BAN103 gene is a single copy in the Chinese cabbage genome, and divided into three exons by two introns. The deduced sequence of 68 amino acids showed a homology with the Brassica oleracea pollen coat protein, as well as several cold-induced proteins. BAN103 transcription was restricted in anthers, but not in pistils, sepals, or non-reproductive tissues. Its transcription is also regulated developmentally. It was first detected after microspore releasing; it increased until the pollen matured. The BAN103 gene promoter was fused with a GUS structural gene. This recombinant plasmid was transformed to Chinese cabbage and tobacco. The GUS expression was detected pollen-preferentially in transgenic tobacco plants. The pollen-preferential activity of this promoter was retained within 176 bp from the translation start codon. The GUS transcription and translation were not coincident in transgenic tobacco pollen. GUS transcripts appeared just after microspore release, and that translation started as the pollen began to dry in mature anthers.
我们从大白菜中分离并鉴定了一个花粉优先表达基因BAN103,并分析了其启动子的活性。对包含该全长基因的BAN103 cDNA和基因组克隆进行了测序。BAN103基因在大白菜基因组中为单拷贝,被两个内含子分隔为三个外显子。推导的68个氨基酸序列与甘蓝花粉壁蛋白以及几种冷诱导蛋白具有同源性。BAN103转录仅限于花药,而在雌蕊、萼片或非生殖组织中不转录。其转录也受发育调控。在小孢子释放后首次检测到它;其表达量一直增加直到花粉成熟。将BAN103基因启动子与GUS结构基因融合。将该重组质粒转化到大白菜和烟草中。在转基因烟草植株中检测到GUS花粉优先表达。该启动子的花粉优先活性在翻译起始密码子上游176 bp范围内得以保留。在转基因烟草花粉中,GUS转录和翻译并不同步。GUS转录本在小孢子释放后立即出现,而翻译在成熟花药中的花粉开始变干时启动。