棕头蜘蛛猴Atfu-B基因α2结构域缺失剪切异构体的表达及其细胞内定位
作者:
基金项目:

31071987, 31272387


Expression and cellular localization of Splice variants of Ateles fusciceps gene Atfu-B with α2 domain deletion
Author:
Fund Project:

31071987, 31272387

  • 摘要
  • | |
  • 访问统计
  • |
  • 参考文献
  • | |
  • 引证文献
  • | |
  • 文章评论
    摘要:

    目的 Atfu-B*sv1是棕头蜘蛛猴主要组织相容性复合体(major histocompatibility complex,MHC)I类分子的一种剪切异构体,其α2结构域缺失。本实验旨在初步获得其在细胞内的表达和定位信息,并与全长的Atfu-B基因的表达情况进行比较, 观察两者之间的差异。方法 分别构建Atfu-B*sv1以及全长Atfu-B基因Atfu-B*02:03和Atfu-B*03:01的真核表达载体,并将这三种重组质粒分别转染293T细胞。利用western-blot免疫印迹实验检测这三种基因在细胞内的表达情况,并利用免疫荧光和激光共聚焦显微镜技术分别分析这三种基因在细胞内的表达定位。 结果 Atfu-B*sv1、Atfu-B*02:03和Atfu-B*03:01均能在293T细胞内正常表达,并且都发生了糖基化的修饰,三种基因都在细胞膜上表达。结论 虽然Atfu-B*sv1的α2结构域缺失,但其细胞内的表达和定位与全长全长Atfu-B基因没有明显差异,其功能有待于进一步探索。

    Abstract:

    Objective Atfu-B*sv1 with α2 domain deletion is a splice variant of major histocompatibility complex class I B in Ateles fusciceps. In this experiment the basic information about expression and cellular location of Atfu-B*sv1 was got, and aimed at compared with the full-length Atfu-B genes, observed the different from them. Methods Eukaryotic expression vectors of Atfu-B*sv1、 Atfu B*02:03 and Atfu-B*03:01 were constructed and transfected to 293T cells. The expressions of the three genes in cells were detected by Western blotting methods, and the cellular locations of the three genes were analyzed by immunofluorescence and laser confocal microscopy. Results Atfu-B*sv1、Atfu-B*02:03 and Atfu-B*03:01 were all expressed in the 293T cell and were glycosylation . All the three genes were expressed on the cell membrane. Conclusion The expression and cellular localization of Atfu-B*sv1 was not significantly different from the full length Atfu-B genes. Further researches about functions of Atfu-B *sv1 need to be done.

    参考文献
    相似文献
    引证文献
引用本文

曹玉华.棕头蜘蛛猴Atfu-B基因α2结构域缺失剪切异构体的表达及其细胞内定位[J].中国比较医学杂志,2013,23(10).

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2013-09-03
  • 最后修改日期:2013-09-12
  • 录用日期:2013-10-14
  • 在线发布日期: 2013-12-16
防诈骗提示!请勿点击不明链接或添加个人微信。编辑部所有邮箱后缀均为@cnilas.org
关闭