4.2 Article

Association study between gene polymorphisms in PPAR signaling pathway and porcine meat quality traits

期刊

MAMMALIAN GENOME
卷 24, 期 7-8, 页码 322-331

出版社

SPRINGER
DOI: 10.1007/s00335-013-9460-4

关键词

-

资金

  1. National Natural Science Foundation of China [31072003, 3100992, 31101706, 31272414]
  2. National High Technology Research and Development 863 Program of China [354, 2008AA101009, 2006AA10Z1E3]
  3. National Key Basic Research 973 Program of China [2006CB102102]
  4. National 948 Project of China [2012-Z26, 2011-G2A]

向作者/读者索取更多资源

There is increasing evidence suggesting that fatty acids biosynthesis and metabolism are regulated by peroxisome proliferator-activated receptors (PPARs), mostly through the PPAR signaling pathway at the transcriptomic level. We hypothesized that the genetic variants of the enzymes in the PPAR signaling pathway may be associated with the traits of porcine meat quality (PMQ). We mined 77 potentially functional single nucleotide polymorphisms in the PPAR signaling pathway of the pig. There were 13 TagSNPs in 13 different genes mapped within the reported pig quantitative trait loci (QTLs) regions related to PMQ based on the Pig QTL database. Based on the association study with ten measured PMQ traits in both the pathway level and the SNP level, we tested eight significantly associated traits with additive effect in the PPAR signaling pathway and explored only one significant TagSNP in gene RXRB, which is directly associated with the trait of skin weight. Moreover, several interactions of TagSNPs were also significantly related to some of PMQ traits. In this large and comprehensive candidate gene set study, we found a modest association of genes and SNPs in the PPAR signaling pathway with PMQ. Further investigation of these gene polymorphisms jointly with fatty acid measures and other genetic factors would help us better understand the regulation mechanisms of PMQ.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据