期刊文献+

鸭CYP7A1基因编码区C129T突变对肉质和脂肪性状的遗传效应分析 被引量:3

C129T mutation of CYP7A1 gene coding region and its genetic effects on meat quality and fatness traits in duck
下载PDF
导出
摘要 采用PCR—SSCP法检测3个鸭群体CYP7A1基凶编码区87~246bp区域多态性.分析其多态性对肉质和脂肪性状的关联性。结果表明:金定鸭和兴义鸭群体中没有检测到多态性,全部为|厂r基因型;樱桃谷鸭群体中检测到TT和TC2种基因型.TT基因型频率为0.8909,T等位基因频率为0.9454;序列比对发现,c.129C〉T沉默突变,表现为低度多态,处于Hardy—Weinberg平衡状态(P〉O.05),T-检验显示,TT基因型个体的肌内脂肪和血清总胆固醇显著低于TC基因型个体,其他指标在两个基因型问的差异均未达到鼹著水平。揭示等位基因C町能是脂肪沉积的有利等位基因,可作为提高肉鸭肌内脂肪的选择性标记。 The polymorphism of from 87 bp to 246 bp of CYP7A 1 gene coding region of three duck populations was detected by PCR-SSCP method, and then its association with meat quality and fatness traits were further analyzed. The results indicated that two genolypes (TT and TC) were observed in Cherry Valley duck. TT genotype and T allele frequencies were 0.8909 and 0.9454, respectively. c.129C〉T of silent mutation was found, which belonged to low polymorphism, and it was in accordance with Hardy-Weinberg equilibrium. The polymorphism hadn't been checked in Jingding duck and Xingyi duck. T-test revealed that intramuscular fat and serum total cholesterol with TI" genotype had significant lower than TC genotype. Other traits were no significant difference between two genotypes. These results suggest tha', callele might be advantage allele for fat deposition and could be used as a genetic marker for improving duck intramuscular fat.
出处 《广东农业科学》 CAS CSCD 北大核心 2012年第24期158-160,共3页 Guangdong Agricultural Sciences
基金 国家自然科学基金(31160453) 贵州大学博士基金(贵大人基合字[2010]037号) 贵州大学大学生创新性实验计划(贵大创字[2011]067号)
关键词 CYP7A1 PCR-SSCP 遗传效应 duck CYP7A 1 PCR-SSCP genetic effects
  • 相关文献

参考文献5

二级参考文献40

共引文献79

同被引文献56

  • 1柳晓峰,李辉.PPAR基因与脂肪代谢调控[J].遗传,2006,28(2):243-248. 被引量:22
  • 2董艳,张宏利,冯绮文,陈雪茹,苏青.人PCK1基因克隆及其表达载体的构建[J].上海交通大学学报(医学版),2006,26(2):135-137. 被引量:1
  • 3杨垄.鹅CYP7A1基因克隆、表达调节及表达规律的研究[D].武汉:华中农业大学,2010.
  • 4Cohen J C,Cali J J,Jelinek D F,et al. Cloning of the hu- man cholesterol 7 alpha-hydroxylase gene(CYP7) and localiza- tion to chromosome 8ql 1-q12 [J]. Genomics, 1992, 14 (1) : 153- 161.
  • 5Norllin M,Wikyall K. Enzymes in the conversion of choles- terol into bile acids[J], Curt Mole Meal,2007,7(2): 199-218.
  • 6Pullinger C R,Eng C,Salen G,et al. Human cholesterol 7a- hydroxylase (CYP7A1)deficiency has a hypercholesterolemic phe- notype [ J ]. J Clin Invest, 2002,110( 1 ) : 109-117.
  • 7Horfman A. Mechanisms of bile acid biosynthesis regulation-autoregulation by bile acids [J]. Postepy Biochem, 2011,57 (3) : 314-323.
  • 8Miao J,Choi S E,Seok S M,et al. Ligand-dependent regula- tion ff theactivity of the orphan nuclear receptor, small het- erodimer partner(SHP), in the repression of bile acid biosyn- thetic CYP7A1 and CYP8B1 genes[J]. Mol Endocrinol,2011,25 (7) : 1159-1169.
  • 9Srivastava A, Malhotra Y. Study of lanthanum incorporated HfO2 nano-scale high--k dielectric using dense plasma focus for metal- insulator- metal capacitor applications [C ]//Proceedings of the 10th WSEAS International Conference on Signal Process- ing,2011 : 159-161.
  • 10Chiang J Y. Bile acids: regulation of synthesis[J]. J Lipid Res,2009,50(10) : 1955--1966.

引证文献3

二级引证文献14

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