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广西师范大学学报(自然科学版) ›› 2013, Vol. 31 ›› Issue (4): 121-127.
蒋骄云1,2, 冯龙2, 曲宪成2, 田文斐2
JIANG Jiao-yun1,2, FENG Long2, QU Xian-cheng2, TIAN Wen-fei2
摘要: 本文运用cDNA末端快速扩增(Rapid-amplification of cDNA ends,RACE)技术、半定量RT-PCR技术和原位杂交技术,克隆黄鳝Monopterus albus性腺差异表达基因(F4)的cDNA全长序列,并分析该基因于各期性腺组织的表达情况。结果显示:F4基因cDNA全长2 466 bp,含有142 bp的5'-UTR、596 bp的3'-UTR、1 728 bp的开放阅读框(ORF),共编码575个氨基酸;在线Signal P分析表明,F4亚基肽链不存在信号肽,为非经典分泌蛋白;同源性分析结果显示该基因无同源性序列,视为新报道的基因;F4在卵巢发育早期不表达,从排卵的Ⅳ期卵巢开始表达,随着卵巢的败育和精巢的发育,表达量明显升高。性逆转过程中差异表达基因的克隆和鉴定,为进一步探究黄鳝性别调控机制奠定了基础。
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