畜牧兽医学报 ›› 2015, Vol. 46 ›› Issue (6): 889-895.doi: 10.11843/j.issn.0366-6964.2015.06.003

• 遗传繁育 • 上一篇    下一篇

公鸡弱精症相关候选基因的表达分析

富丽1,2,孙研研2,薛夫光2,刘冉冉2,白皓2,常国斌1,陈国宏1,陈继兰2*   

  1. 富丽(1988-),女,山东烟台人,硕士,主要从事家禽分子遗传研究,Tel:010-62816005,E-mail:momomook@126.com
  • 收稿日期:2014-08-15 出版日期:2015-06-23 发布日期:2015-06-23
  • 通讯作者: 陈继兰,研究员,E-mail:Chen.jilan@163.com
  • 作者简介:富丽(1988-),女,山东烟台人,硕士,主要从事家禽分子遗传研究,Tel:010-62816005,E-mail:momomook@126.com
  • 基金资助:

    国家自然科学基金(31372304);中国农业科学院科技创新工程(ASTIP-IAS04)

The Expression of the Six Candidate Genes for Asthenospermia of the Rooster

FU Li1,2,SUN Yan-yan2,XUE Fu-guang2,LIU Ran-ran2,BAI Hao2,CHANG Guo-bin1,CHEN Guo-hong1,CHEN Ji-lan2*   

  1. (1.扬州大学动物科学与技术学院,扬州 225009;2.中国农业科学院北京畜牧兽医研究所,农业部畜禽资源与种质创新重点实验室,北京 100193)
  • Received:2014-08-15 Online:2015-06-23 Published:2015-06-23

摘要:

为了探究公鸡弱精症的发病机理,本研究对前期应用数字基因表达谱技术(Digital gene expression,DGE)及生物信息学分析得到的与公鸡弱精症相关的6个候选基因(COX7BPTGDShPGDSSPAG6、WNT2、CCNF)进行表达分析。选取300只42周龄的北京油鸡公鸡,进行为期4周的精液品质检测,从中筛出弱精及正常个体各15只。采用RT-qPCR对这6个候选基因在两组个体的睾丸组织的表达量进行相对定量检测。结果发现,COX7BPTGDS在弱精组个体睾丸的表达量显著高于正常个体(P<0.01),WNT2、hPGDSCCNF在弱精组个体的表达量显著低于正常个体(P<0.05),SPAG6在两组睾丸中的表达量没有显著差异,该结果与DGE的结果相吻合。通过DGE筛选出与弱精症相关的6个候选基因的表达模式在本研究的群体中得到进一步验证,可作为公鸡弱精症的重要候选基因,进一步进行功能分析与验证,为揭示公鸡弱精症的发病机理提供依据。

Abstract:

To explore the pathogenesis of the rooster asthenospermia,the expression profiles of 6 candidate genes (COX7BPTGDShPGDSSPAG6,WNT2 and CCNF) selected from the previous digital gene expression profiling (DGE) and bioinformatics analysis,were analyzed.A total of 300 Beijing-You roosters of 42 weeks were detected for 4 weeks for semen quality including semen volume,sperm mobility,etc.Fifteen asthenospermia and 15 normal roosters were selected accordingly.Real-time quantitative PCR were performed to determine the expression of the 6 genes in the testicular of those roosters.The results indicated that COX7B and PTGDS were significantly high-expressed in the asthenospermia group (P<0.01),while the WNT2,hPGDS and CCNF were significantly low-expressed in the asthenospermia group (P<0.05).However,the expression of SPAG6 gene was not significantly different in the 2 groups.These results were in accordance with the previous DGE analysis.The expression patterns of the 6 genes identified from DGE for asthenospermia in chickens were validated in the present study.They can be important candidate genes for further functional study and revealing the mechanism of chicken asthenospermia.

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