中国农业科技导报 ›› 2019, Vol. 21 ›› Issue (3): 42-47.DOI: 10.13304/j.nykjdb.2018.0137

• 生物技术 生命科学 • 上一篇    下一篇

小鼠黑色素瘤功能异常CD8+ T细胞基因调控网络构建与分析

韩鹏勇1,2,塔娜1,宝鲁日1,于海泉1*   

  1. 1.内蒙古大学省部共建草原家畜生殖调控与繁育国家重点实验室, 呼和浩特 010070; 2.长治医学院, 山西 长治 0460007
  • 收稿日期:2018-03-09 出版日期:2019-03-15 发布日期:2018-05-24
  • 通讯作者: *通信作者:于海泉,研究员,博士生导师,主要从事哺乳动物生殖生物学及生物技术研究。E-mail: haiquan_yu@163.com
  • 作者简介:韩鹏勇,博士研究生,主要从事基因调控网络研究。E-mail: hanpengyong@gmail.com。
  • 基金资助:
    国家自然科学基金项目(31460311);内蒙古自然科学基金项目( 2016ZD01)资助。

Construction and Analysis of Gene Regulatory Network in Dysfunctional CD8+ T Cells

HAN Pengyong1,2, TA Na1, BAO Luri1, YU Haiquan1*   

  1. 1.State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, Inner Mongolia University, Hohhot 010070; 2.Changzhi Medical College, Shanxi Changzhi 046000, China
  • Received:2018-03-09 Online:2019-03-15 Published:2018-05-24

摘要: 疾病是全球范围内危害畜禽健康的主要问题,解析免疫系统调控相关基因成为当前抗病分子育种的研究热点。为研究小鼠黑色素瘤模型功能异常CD8+ T细胞对免疫抗体处理的应答机制,通过基因调控网络方法筛选功能异常CD8+ T细胞在IgG和PD1抗体处理的特定基因、转录因子和细胞表面受体。结果发现对照组、PD1抗体与IgG抗体处理组分别有28、17、33个特定表达基因。与对照组相比,IgG和PD1处理组有2个转录因子Zfx、Zfhx3关闭表达,PD1处理组细胞表面受体Raet1b表达。Raet1b基因的表达可能使小鼠黑色素瘤功能异常CD8+ T细胞恢复功能,结果为抗病育种的相关基因研究提供理论基础。

关键词: 抗病育种, 基因调控网络, 小鼠黑色素瘤, 功能异常CD8+ T 细胞, 特有基因

Abstract: Disease is a major threat to livestock and poultry health worldwide. Identifying key genes related to disease resistance has become a research hotpot in molecular breeding of disease resistance. To better understand the response mechanism of dysfunctional CD8+ T cell to immune therapy treatment, the gene regulatory network was constructed for the dysfunctional CD8+ T cells under PD1, IgG antibody treatments. There were 28, 17, 33 genes being identified in control, IgG and PD1 antibody treatment groups, respectively. Two transcription factors of Zfx and Zfhx3 expressed silencing under treatments of both IgG and PD1. The surface receptor of Raet1b expressed increasingly under treatment of PD1, which might recover dysfunctional CD8+ T cells. This research provided theoretical basis for gene exploring related to disease resistance breeding.

Key words: disease resistance breeding, gene regulatory network, mouse melanoma model, dysfunctional CD8+ T cell, specific gene