期刊文献+

中国地方黄牛PPARα exon7基因多态性与生长性状的关联研究 被引量:2

Polymorphism of the Exon 7 of PPARαGene and Correlation with Growth Traits in Chinese Indigenous Cattle
下载PDF
导出
摘要 [目的]以期为我国地方黄牛生长性状分子育种提供理论依据。[方法]本研究以南阳牛、郏县红牛、鲁西牛和秦川牛4个品种共计424头中国地方黄牛为材料,以与牛脂肪代谢相关的基因PPARα为目标基因,利用生物信息学、PCR-RFLP结合DNA池测序等技术,对其第7外显子(PPARα_exon7)进行遗传特征分析,检测SNPs,并分析该序列的多态性与试验黄牛生长性状指标的相关性。[结果]发现在PPARα基因(AC_000162.1)exon7的164bp处发现了一处SNP(C/T),检测出CC和CT两种基因型。群体遗传分析显示,该位点在试验牛群体中均属于中度多态(0.25<PIC<0.5);关联分析结果显示,该位点在体斜长指标上,两种不同基因型的个体之间有显著的差异(P<0.05)。[结论]表明该位点有可能作为黄牛生长性状辅助选择的标记之一,应用于中国地方黄牛的分子遗传育种工作中。 【Objective】The aim of this study was to provide theoretical basis for the molecular breeding of local cattle growth traits in China.【Method】In order to better understand the effect of PPARαgene which related with bovine fat metabolism in 424 Chinese indigenous cattle samples,including Nanyang cattle(NY),Jiaxian red cattle(JX),Luxi cattle(LX)and Qinchuan cattle(QC).A novel SNP of exon 7locus of the bovine PPARαgene was detected with bioinformatics,PCR-RFLP,and DNA sequencing to investigate the genetic variations of PPARα.In addition,an association study was carried out to determine the effect of the SNPs of PPARαgene in exon 7on the growth and meat quality traits.【Result】As a result,the SNP(C/T)was identified at 164 bp of PPARαgene in exon 7(AC_000162.1),which contained two genotypes(CC and CT).The genetic analysis showed that SNP(C/T)was midrange polymorphism(0.25PIC0.5),and the association analysis of CC and CT genotypes with the growth and development traits indicated that individuals had a significant difference in body length(P 0.05).【Conclusion】Therefore,this SNP(C/T)of PPARαgene in exon 7maybe one marker in selecting individuals with superior growth and meat quality traits,which could be used in molecule breeding for Chinese indigenous cattle.
出处 《中国牛业科学》 2016年第1期1-5,共5页 China Cattle Science
基金 国家自然科学基金(No.31172193) 河南省科技创新人才项目(No.134100510012) 河南省高校科技创新团队项目(No.14IRTSTHN012) 信阳师范学院青年科学基金(2015037)资助
关键词 中国地方黄牛 PPARα基因 SNPS 关联分析 Chinese indigenous cattle PPARα gene SNPs association analysis
  • 相关文献

参考文献14

  • 1Yuan G, Chen X, Li D. Modulation of peroxisome prolifera- tor-activated receptor gamma (PPAR'/) by conjugated fatty acid in obesity and inflammatory bowel disease[J]. Journal of agricultural and food chemistry, 2015, 63(7): 1883-1895.
  • 2Penas F, Mirkin G A, Vera M, et al. Treatment in vitro with PPARa and PPAR7 ligands drives Ml-to-M2 polarization of maerophages from T. cruzi-infeeted mice[J]. Biochimica et biophysica aeta-molecular basis of disease, 2015, 1852(5) : 893-904.
  • 3Falcone R, Florio T M, Di G E, et al. PPAR/3 and 3' in a rat model of parkinson's disease: possible involvement in PD symptoms[J]. Journal of cellular biochemistry, 2015, 116 (5) : 844-855.
  • 4Peng Z, Ban K, Wawrose R A, et al. Protection by enteral glutamine is mediated by intestinal epithelial cell peroxisome proliferator activated receptor gamma during intestinal ische- mia/reperfusion[J]. Shock, 2015, 43(4): 327-333.
  • 5Gu S J, Chen D H, Guo Z R, et al. Effect of obesity on the association between common variations in the PPAR gene and C-reactive protein level in Chinese Han population[J]. Endo- crine, 2015, 48(1): 195-202.
  • 6Van Diepen J A, Jansen P A, Ballak D B, et al. PPAR-alpha dependent regulation of vanin-1 mediates hepatic lipid metab- olism[J]. Journal of Hepatology, 2014, 61(2) : 366-372.
  • 7Montiel P G, Antaramian A, Miyasaka A S, et al. Role of co- activator PGC- la in energy balance: Importance in the pro- duction of beef cattle[J]. Archivos Latinoamericanos de Pro- duccion Animal, 2008, 16(2):63-77.
  • 8Nkrumah J D, Sherman E L, Li C, et al. Primary genome scan to identify putative quantitative trait loci for feedlot growth rate, feed intake, and feed efficiency of beef cattle[J].Journal of Animal Science, 2007, 85 (12): 3170-3181.
  • 9Sebastian L, Beatrice G, Holger K, et al. Clofibrate causes an upregulation of PPAR-atarget genes but does not alter expres- sion of SREBP target genes in liver and adipose tissue of pigs [J]. American Journal of Physiology, 2007 , 293(1) : 70-77.
  • 10樊月圆,昝林森,王洪宝,付常振.牛过氧化物酶体增殖激活受体α(PPARα)基因第5外显子多态性与胴体、肉质性状的相关性[J].农业生物技术学报,2010,18(4):713-718. 被引量:11

二级参考文献54

  • 1邱怀,张英汉.试论牛品种经济类型的形成与划分问题[J].黄牛杂志,1993,19(4):1-4. 被引量:11
  • 2张英汉.国际肉牛育种的新动向-小型肉牛培育[J].中国牛业科学,2006,33(1):1-4. 被引量:3
  • 3胡林勇,南小红,张金川,张英汉.秦川牛部分体量性状的遗传参数估测[J].中国牛业科学,2006,32(4):4-8. 被引量:22
  • 4[1]Lemberger T,B Desvergne,W Wahli.Peroxisome proliferator-activated receptors: A nuclear receptor signaling pathway in lipid physiology.Annu.Rey.Cell Dev.Biol.,1996,12:335~363.
  • 5[2]Schoonjans K,B Staels,J Auwerx,Role of the peroxisome proliferator-activated receptor (PPAR) in mediating the effects of fibrates and fatty acids on gene expression.J.Lip.Res.,1996,37:907~925.
  • 6[3]Isabelle Issemann,Stephen Green.Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators.Nature,1990,347:645~650.
  • 7[4]Dreyer C,G Krey,Keller F,Givel G.Helftenbein,W Wahli.Control of the peroxisomal betaoxidation pathway by a novel family of nuclear hormone receptors.Cell,1992,68: 879~887.
  • 8[5]Wahli W O,Braissant,B Desvergne.Peroxisome proliferator-activated receptors: transcriptional regulators of adipogenesis,lipid metabolism and more.Chem.Biol.,1995,2:261~266.
  • 9[6]Tontonoz P E Hu,B M Spiegelman.Stimulation of adipogenesis in fibroblasts by PPAR-γ 2,a lipid-activated transcription factor.Cell,1994,79:1147~1156.
  • 10[7]Braissant O,Foufelle F,Scotto C et al.Differential expression of peroxisome proliferator-activated receptors (PPARs): Tissue distribution of PPAR-α,-β,and -γ in the adult rat.Endocrinol.,1996,137:345.

共引文献53

同被引文献27

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部