华北农学报 ›› 2012, Vol. 27 ›› Issue (3): 72-74. doi: 10.3969/j.issn.1000-7091.2012.03.014

所属专题: 生物技术

• 论文 • 上一篇    下一篇

MC4R与Leptin、MC3R和CCKAR基因的互作研究

张冬杰, 汪亮, 刘娣   

  1. 黑龙江省农业科学院畜牧研究所, 黑龙江哈尔滨 150086
  • 收稿日期:2012-03-24 出版日期:2012-06-28
  • 通讯作者: 刘娣(1963-), 女, 吉林长春人, 教授, 博士, 主要从事猪遗传育种及家畜生物技术研究。
  • 作者简介:张冬杰(1980-), 女, 黑龙江桦南人, 副研究员, 博士, 主要从事猪分子遗传育种研究。
  • 基金资助:
    转基因生物新品种培育重大专项(2008ZX08006-003);现代农业产业技术体系(CARS-36)

The Interaction of MC4R with Leptin,MC3R and CCKAR Genes

ZHANG Dong-jie, WANG Liang, LIU Di   

  1. Institute of Animal Husbandry, Heilongjiang Academy of Agricultural Sciences, Harbin 150086, China
  • Received:2012-03-24 Published:2012-06-28

摘要: 为了研究4个与采食量相关功能基因可能存在的互作关系,采用基因重组的方法构建了黑素皮质激素受体-4(MC4R)基因的真核表达载体,采用脂质体法将该表达载体转染入成纤维细胞,瞬时转染24 h后,采用Real-timePCR的方法检测和分析了Leptin、黑素皮质激素受体-3(MC3R)和猪缩胆囊素受体(CCKAR)基因mRNA的表达变化情况。结果表明,在成纤维细胞中,过表达MC4R基因后,Leptin、MC3RCCKAR基因的mRNA水平均无显著变化。据此推测,MC4R基因与其他3个基因虽都参与调节动物的采食量,但很可能是通过不同的调控路径来发挥功能的。

关键词: 猪, 成纤维细胞, MC4R, Real-timePCR, 过表达

Abstract: To study the potential relationships among the four genes associated with intake,recombinant method?was used to build a Melanocortin receptor-4 (MC4R) gene eukaryotic expression vector. The expression vector was?transfected into fibroblasts by liposome method. Transient transfection after 24 h,Real-time PCR method was used to?detect and analyze Leptin,MC3R and CCKAR mRNA expression changes. The results showed that,in fibroblasts,?overexpression of MC4R gene,Leptin,MC3R and CCKAR mRNA levels were not significantly changed. Presumed?that although these four genes are all involved in the regulation of animal feed intake,but they are likely to be regulated by a different pathway.

Key words: Pig, Fibroblasts, MC4R, Real-time PCR, Overexpression

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引用本文

张冬杰, 汪亮, 刘娣. MC4R与Leptin、MC3R和CCKAR基因的互作研究[J]. 华北农学报, 2012, 27(3): 72-74. doi: 10.3969/j.issn.1000-7091.2012.03.014.

ZHANG Dong-jie, WANG Liang, LIU Di. The Interaction of MC4R with Leptin,MC3R and CCKAR Genes[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2012, 27(3): 72-74. doi: 10.3969/j.issn.1000-7091.2012.03.014.

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