CODEHOP法设计引物克隆中华绒螯蟹5-ht_1和5-ht_2受体基因片段及序列分析  被引量:3

CODEHOP PCR primers for cloning 5-ht_1 and 5-ht_2 receptor fragments in Eriocheir sinensis

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作  者:徐泽文[1] 杨筱珍[1] 黄坚[1] 李彤[1] 杨志刚[1] 王春[1] 成永旭[1] 

机构地区:[1]上海海洋大学水产种质资源发掘与利用教育部重点试验室,上海201306

出  处:《生物学杂志》2015年第1期1-5,共5页Journal of Biology

基  金:国家自然科学基金(31272677);国家农业科技成果转化项目(2012GB2C000147);上海市科委科技合作专项(13231203504);上海市学术带头人计划(12XD1402700)

摘  要:根据已报道的中华绒螯蟹近缘物种的5-ht1r和5-ht2r氨基酸序列保守区,利用CODEHOP设计了两对简并引物,采用RT-PCR法扩增得到了中华绒螯蟹5-ht1r和5-ht2r部分片段并克隆到p MD-19T载体。测序结果表明扩增到的中华绒螯蟹5-ht1r和5-ht2r片段长分别为366 bp和177 bp,编码121和58个氨基酸。经BLASTp分析显示,中华绒螯蟹5-ht1r与罗氏沼虾(Macrobrachium rosenbergii)和克氏原螯虾(Procambarus clarkii)的5-ht1r同源性高达98%,而中华绒螯蟹5-HT2R与断沟龙虾(Panulirus interruptus)和克氏原螯虾(Procambarus clarkii)5-ht2r同源性高达95%。According to the conserved amino acid sequences of known 5-Hydroxytryptamine receptors,CODEHOP( Consensus Degenerate Hybrid Oligonucleotide Primers) software was used to design degenerate primers to obtain partial c DNA fragments of 5-HT1 and 5-HT2receptors( 5-ht1 r and 5-ht2r) in Chinese mitten crab( Eriocheir sinensis). The fragments of5-ht1 r and 5-ht2 r were amplified by reverse transcription polymerase chain reaction( RT-PCR) and then cloned into p MD-19 T vector. The sequencing results revealed that 5-ht1 r and 5-ht2 r fragments contain 366 and 177 base pairs,which encode 121 and 58 amino acids respectively. BLAST analysis indicated that the amino acid homology of 5-ht1 r was 98% similar to Macrobrachium rosenbergii and Procambarus clarkia,and the 5-ht2 r was most similar to Panulirus interruptus and Procambarus clarkia( 95%).

关 键 词:CODEHOP 中华绒螯蟹 5-ht1r 5-ht2r 克隆 

分 类 号:Q78[生物学—分子生物学] S917.4[农业科学—水产科学]

 

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