Nakaniwa Makiko, Hirayama Makoto, Shimizu Atsushi, Sasaki Takashi, Asakawa Shuichi, Shimizu Nobuyoshi, Watabe Shugo
Laboratory of Aquatic Molecular Biology and Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.
J Exp Biol. 2005 May;208(Pt 10):1915-25. doi: 10.1242/jeb.01570.
Medaka genomic BAC clones, which contained two types of medaka hemopexin-like protein gene (Wap65), mWap65-1 and mWap65-2, were screened and their genomic sequences were determined by the shotgun strategy. The exon-intron organizations were highly conserved between both mWap65s and human hemopexin genes. The 5'-flanking regions of mWap65-1 and mWap65-2 contained various putative transcription factor binding sites including elements for developmental regulation. The expression patterns of mWap65s during embryonic development were examined by quantitative real-time PCR, demonstrating that both mWap65 transcripts were observed in early embryonic stages, but their expression patterns were different. Interestingly, in situ hybridization revealed that mWap65-2 transcripts were restricted to liver, whereas mWap65-1 transcripts were detected along the edge of pectoral fin buds and the median fin fold of tail buds in embryos at stage 32. Furthermore, we generated transgenic medaka expressing GFP driven by mWap65-1 and mWap65-2 promoters and observed GFP expression patterns during ontogeny. Although localizations of GFP varied among individuals, embryos uniformly expressed GFP 1 day after injection of mWap65-1-hrGFP and mWap65-2-hrGFP constructs, suggesting that mWap65-1 and mWap65-2 promoters were activated in very early stages. The differences between mWap65-1 and mWap65-2 in their expression profiles indicate their distinct roles during ontogeny.
筛选出包含两种青鳉血色素结合蛋白样蛋白基因(Wap65),即mWap65 - 1和mWap65 - 2的青鳉基因组BAC克隆,并通过鸟枪法策略测定其基因组序列。两种mWap65基因与人血色素结合蛋白基因之间的外显子 - 内含子组织高度保守。mWap65 - 1和mWap65 - 2的5'侧翼区域包含各种推定的转录因子结合位点,包括发育调控元件。通过定量实时PCR检测mWap65在胚胎发育过程中的表达模式,结果表明在胚胎早期阶段均观察到两种mWap65转录本,但它们的表达模式不同。有趣的是,原位杂交显示mWap65 - 2转录本仅限于肝脏,而在第32阶段的胚胎中,mWap65 - 1转录本在胸鳍芽边缘和尾芽的中鳍褶处被检测到。此外,我们构建了由mWap65 - 1和mWap65 - 2启动子驱动表达GFP的转基因青鳉,并观察了个体发育过程中的GFP表达模式。尽管GFP的定位在个体间有所不同,但在注射mWap65 - 1 - hrGFP和mWap65 - 2 - hrGFP构建体1天后胚胎均表达GFP,这表明mWap65 - 1和mWap65 - 2启动子在非常早期阶段就被激活。mWap65 - 1和mWap65 - 2在表达谱上的差异表明它们在个体发育过程中具有不同的作用。