| 陈艳萍 王立红 高春萍 晋慧 周进.黑鲷转铁蛋白基因的分子特征研究[J].,2014,14(27):5225-5229 |
| 黑鲷转铁蛋白基因的分子特征研究 |
| Molecular Cloning and Function Characterization of Transferrin fromAcanthopagrus Schlegeli |
| |
| DOI： |
| 中文关键词: 黑鲷 转铁蛋白 全基因克隆 分子特征 |
| 英文关键词: Black Seabream Transferrin Homology cloning Molecular characterization |
| 基金项目:天津市滨海新区科技小巨人成长计划项目(2011-XJR12065)；深圳南山区创新研发项目（KC2013JSCX0003A） |
|
| 摘要点击次数: 649 |
| 全文下载次数: 854 |
| 中文摘要: |
| 目的：克隆黑鲷转铁蛋白全基因并分析其分子特征。方法：采用同源克隆的方法，对黑鲷转铁蛋白全基因编码序列进行克
隆，在cDNA 获得了部分转铁蛋白基因的同源片段。经RACE PCR 方法，分别对该基因的3’和5’末端进行扩增,获得的扩增片段
经拼接后得到全基因片段。结果：黑鲷转铁蛋白全长2431bp，可编码691 个氨基酸，分子量(MW)约为74.3kDa，等电点(PI)为5.63。
它与鱼类转铁蛋白的同源性最高，约为65%-89%>；与其它动物（哺乳类、两栖类等）也有一定的相识性。进化分析表明黑鲷转铁蛋
白与其它鱼类和哺乳类的转铁蛋白是由早期转铁蛋白共同的祖先进化来的。结论：黑鲷转铁蛋白主要在肝脏中成组成型表达，在
大脑等器官中也有少量表达。该基因的表达受病原刺激的影响，表现为经病原刺激后转铁蛋白基因的组织分布显著增多。 |
| 英文摘要: |
| Objective:To clone and to analyze the molecular characterization of transferrin from Black seabream(Acanthopagrus
schlegeli).Methods:The full length transferrin (TF) gene from Black Seabream was cloned by homology strategy using a pair of
degenerated primers designed according to the conserved regions of other animals' TF genes. A part of homologous fragment was
obtained by PCR amplification, the fragment was elongated by RACE PCR with the adaptor primer and several gene specific primers to
get the full length sequence.Results:The sequence contained 2431 bp including a short 5' UTR of 31 bp and 3' UTR of 341bp and an
open reading frame of 2072 bp which could code a 691 amino acids peptide with putative MWof 74.3kDa and putative PI of 5.63. The
sequence shared high identity and similarity with other animals' transferrin, especially with the fish TF genes. There was about 65-89%
identities with other fish, and about 40-50% identities with each of the mammalian TFs.Conclusion:Phylogenetic analysis showed that
the TF gene evolution from the same ancestor with the others animals' transferrin. RT-PCR showed that the Black Seabream TF was
constitutively expressed in liver, and it could be regulated by pathogen stimulating, the distribution of TF expression increased
significantly after pathogen stimulating. |
|
查看全文
查看/发表评论 下载PDF阅读器 |
| 关闭 |
