畜牧兽医学报 ›› 2014, Vol. 45 ›› Issue (3): 375-379.doi: 10.11843/j.issn.0366-6964.2014.03.005

• 遗传繁育 • 上一篇    下一篇

转录因子Sox-5负调控猪S100A12基因表达

徐静,唐娟,刘映,赵书红,李新云*   

  1. (华中农业大学动物科技学院 农业动物遗传育种与繁殖教育部重点实验室,武汉 430070)
  • 收稿日期:2013-07-05 出版日期:2014-03-23 发布日期:2014-03-23
  • 通讯作者: 李新云,副教授,E-mail:xyli@mail.hzau.edu.cn
  • 作者简介:徐静 (1988-),女,湖北武汉人,硕士生,主要从事动物遗传育种研究,E-mail:hzauxujing@163.com
  • 基金资助:

    教育部新教师基金项目(20090146120032);国家自然科学基金资助项目(30901020);863项目(2013AA102502)

The Transcription of S100A12 Gene Negatively Regulated by Sox-5 in Pig

XU Jing,TANG Juan,LIU Ying,ZHAO Shu-hong,LI Xin-yun*   

  1.  (Key Laboratory of Agricultural Animal Genetics,Breeding and Reproduction of Ministry of Education,Huazhong Agricultural University,Wuhan 430070, China)
  • Received:2013-07-05 Online:2014-03-23 Published:2014-03-23

摘要:

本研究旨在确定猪S100A12启动子-1 013~-590区域中起负调控作用的转录因子。首先,通过双荧光素酶报告系统对猪S100A12启动子-1 013~-590区域转录活性进行研究,分别对S100A12启动子-1 013~+598、-931~+598、-830~+598、-711~+598和-590~+598转录活性进行检测。然后对-1 013~-931关键区域进行进一步缺失及突变研究,鉴定该区域负调控S100A12基因的转录因子及其结合位点。结果表明,猪S100A12启动子-1 013~-931区域缺失后,转录活性显著上升,表明该区域存在负调控猪S100A12基因转录因子结合位点。生物信息学手段预测发现,在-1 013~-931区域内存在1个Sox-5,2个GATA-1转录因子结合位点。当转录因子Sox-5结合位点进行缺失及突变时,猪S100A12转录活性显著上升。结果显示转录因子Sox-5负调控猪S100A12基因的表达。

Abstract:

This study aimed to investigate the negative transcriptional factors and their binding motifs in the promoter region of porcine S100A12 gene.The promoter transcriptional activity of the regions,which contains -1 013-+598,-931-+598,-830-+598,-711-+598 and -590-+598 were detected by dual luciferase assay system.Furthermore,the transcriptional activity and the transcriptional factors’ binding sites located in the -1 013--931 region was deeply investigated through DNA deletion and mutation analyses.Porcine S100A12 promoter activity decreased significantly(P<0.05)when the region -1 013--931 was deleted.Bioinformatics analyses results showed that transcriptional factor Sox-5 and GATA-1 binding sites located in this region.The promoter activity was significantly increased only when the binding site of Sox-5 was mutant or deleted.The results indicate that the expression of S100A12 gene is negatively regulated by the transcriptional factor Sox-5.

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