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内蒙古绒山羊褪黑激素受体1a基因外显子1 克隆及序列分析
引用本文:孙永明,张燕军,李国华,刘志红,王志英,于新蕾,赵艳红.内蒙古绒山羊褪黑激素受体1a基因外显子1 克隆及序列分析[J].中国畜牧兽医,2011,38(5):82-84.
作者姓名:孙永明  张燕军  李国华  刘志红  王志英  于新蕾  赵艳红
作者单位:1. 内蒙古大学生命科学院, 内蒙古呼和浩特 010020;2. 内蒙古农业大学动物科学学院, 内蒙古呼和浩特 010018;3. 锡林浩特市毛登牧场, 内蒙古锡林浩特 026000;4. 翁牛特旗畜牧业现代化办公室, 内蒙古乌丹 024500
基金项目:国家自然科学基金,内蒙古自然科学基金,内蒙古农业大学博士科研启动基金
摘    要:参考GenBank上已发表的绵羊(登录号:15U14109)、人(登录号:U14108)、牛(登录号:U73327)、鼠(登录号:U52222)等物种褪黑激素受体(melatonin receptor 1a,MTNR1a)基因 cDNA序列设计引物,以内蒙古绒山羊基因组DNA为模板进行PCR扩增,得到257 bp的基因片段,将扩增产物进行克隆测序后与GenBank数据库进行序列同源性比较。结果表明,绒山羊MNTR1a基因外显子1序列与已发表的绵羊和牛该基因序列同源性分别为99%和96%,说明所得到的序列为绒山羊MNTR1a基因的外显子1序列。利用DNAStar软件分析,得到该基因序列的257个核苷酸。该序列包括5''UTR 23个核苷酸、翻译起始密码子ATG和N端78个氨基酸编码序列。

关 键 词:绒山羊  褪黑激素受体基因  克隆  序列分析  
收稿时间:2010-10-25

Cloning and Sequence Analysis of Exon1 MTNR1a Gene of Inner Mongolian Cashmere Goat
SUN Yong-ming,ZHANG Yan-jun,LI Guo-hua,LIU Zhi-hong,WANG Zhi-ying,YU Xin-lei,ZHAO Yan-hong.Cloning and Sequence Analysis of Exon1 MTNR1a Gene of Inner Mongolian Cashmere Goat[J].China Animal Husbandry & Veterinary Medicine,2011,38(5):82-84.
Authors:SUN Yong-ming  ZHANG Yan-jun  LI Guo-hua  LIU Zhi-hong  WANG Zhi-ying  YU Xin-lei  ZHAO Yan-hong
Institution:1. College of Life Science, Inner Mongolia University,Hohhot 010020,China;2. College of Animal Science, Inner Mongolia Agricultural University,Hohhot 010018,China;3. Maodeng Pasture in Xilinhaote, Xilinhaote 026000,China;4. Wengniute County Animal Husbandry Modernization Offices, Wudan 024500,China
Abstract:According to MTNR1a cDNA sequence of sheep(gi:15U14109), human(gi:U14108), cattle(gi:U73327), mice(gi:U52222) and other species announced in GenBank,primers were designed. The 275 bp fragment of exon 1 of MTNR1a gene was amplified by PCR in Inner Mongolian Cashmere goat. The PCR products were cloned and sequenced. By compared with database of GenBank, it turned out that homology of nucleotide sequence of exon 1 MTNR1a gene in Cashmere goat with sheep, cow were 99% and 96%, respectively. It showed that the sequence was MTNR1a gene exon 1 sequence in Cashmere goat. Using DNAStar software to analysis, 257 nucleotides of the gene sequence was gotten.The sequence contained 5''UTR 23 nucleotides, translation initiation codon ATG and the N terminal 78 amino acid coding sequences.
Keywords:Cashmere goat  MTNR1a gene  cloning  sequence analysis 
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