畜牧与饲料科学 ›› 2016, Vol. 37 ›› Issue (10): 8-8.doi: 10.12160/j.issn.1672-5190.2016.10.003

• 基础科学 • 上一篇    下一篇

牛RPLP1基因的克隆和生物信息学分析

杨翰林;张达;张群;薛光;田万年   

  1. 吉林农业科技学院动物科技学院,吉林古林132101
  • 出版日期:2016-10-20 发布日期:2016-10-20
  • 通讯作者: 杨翰林
  • 作者简介:杨翰林(1996-),男,所学专业为野生动物与自然保护区管理. 通讯作者:田万年(1980-),男,讲师,博士,主要研究方向为动物分子遗传育种。
  • 基金资助:
    吉林农业科技学院大学生科技创新项目(吉农院合字[2015]第052号)

Cloning and Bioinformatics Analysis of the RPLP1 Gene in Cattle

YANG Han-lin, ZHANG Da, ZHANG Qun, XUE Guang, TIAN Wan-nian (College of Animal Science and Technology,Jilin Agricultural Science and Technology University,Jilin 132101 ,China)   

  • Online:2016-10-20 Published:2016-10-20

摘要: 采用RT-PCR法克隆牛RPLP1基因,利用生物信息学分析软件对该基因进行生物信息学分析,应用半定量RT-PCR方法对该基因的组织表达谱进行分析。结果表明,牛RPLP1基因全长为502 bp,包含345 bp的编码区序列,编码114个氨基酸;拓扑预测表明,RPLP1蛋白可能存在3个酪蛋白激酶Ⅱ磷酸化位点,2个豆蔻酰化位点,含有一个Ribosomal-P1保守结构域;牛RPLP1基因在多种组织中均表达,在骨骼肌、肝脏和心肌中表达量较高。

Abstract: In the present study,the RPLP1 gene was cloned by RT-PCR assay and was subsequently bioinformatically analyzed with bioinformatics analysis software,and the tissue expression profile of this gene was determined by semi-quantitative RT-PCR method.The results showed that cattle RPLP1 gene was composed of 502 nucleotides,including a single open reading frame of345 bp which encoded 114 amino acids;topology prediction analysis showed that there were three casein kinase Ⅱphosphorylation sites,two N-myristoylation sites and one Ribosomal-P1 conserved domain in RPLP1 protein;semi-quantitative RT-PCR assay showed that RPLP1 gene was widely expressed,and high expression was observed in skeletal,liver and cardiac muscle.

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