...
首页> 外文期刊>Physiological genomics >The bovine PPARGC1A gene: molecular characterization and association of an SNP with variation of milk fat synthesis
【24h】

The bovine PPARGC1A gene: molecular characterization and association of an SNP with variation of milk fat synthesis

机译:牛PPARGC1A基因:SNP的分子表征和与乳脂合成变化的关系

获取原文
获取原文并翻译 | 示例

摘要

Several studies in a variety of breeds have reported at least two QTL for milk production traits, including milk fat synthesis on bovine chromosome 6 (BTA6), comprising a region that comparatively has been mapped to equivalent syntenic chromosome intervals in human, pig, and mouse harboring loci associated with type II diabetes and obesity-related traits. We identified the bovine peroxysome proliferator-activated receptor- coactivator-1 gene (PPARGC1A) as a plausible positional and functional candidate gene for a previously described QTL for milk fat yield on BTA6 because of its chromosomal position and its key role in energy, fat, and glucose metabolism. To analyze the role of the bovine PPARGC1A gene in regulation of milk fat synthesis in dairy cattle, we determined its cDNA sequence, genomic organization, chromosomal localization, and expression pattern. The bovine PPARGC1A gene is organized in 13 exons comprising 6,261 bp and is expressed at different levels in a large number of tissues. Bovine PPARGC1A cDNA and protein sequences showed substantial similarity (92–95%) to its respective orthologs from human, rat, and mouse. Screening for polymorphisms in the coding sequence, exon/intron boundaries, 5'- and 3'-untranslated regions, and promoter region of the PPARGC1A gene in sires with a different genotype at the QTL for milk fat yield as well as in a multibreed panel revealed a total of 11 polymorphic loci. A significant association between an SNP in intron 9 of the PPARGC1A gene and milk fat yield was observed in a major dairy cattle population, indicating that the PPARGC1A gene could be involved in genetic variation underlying the QTL for milk fat synthesis on BTA6.
机译:多个品种的多项研究报告了至少两个关于牛奶生产性状的QTL,包括牛染色体6(BTA6)上的牛奶脂肪合成,该区域包含一个已被映射到人,猪和小鼠等价同系染色体间隔的区域携带与II型糖尿病和肥胖相关性状有关的基因座。我们将牛过氧化物酶体增殖物激活受体共激活因子1基因(PPARGC1A)鉴定为先前描述的BTA6乳脂产量QTL的合理位置和功能候选基因,因为它的染色体位置及其在能量,脂肪,和葡萄糖代谢。为了分析牛PPARGC1A基因在调节奶牛乳脂合成中的作用,我们确定了其cDNA序列,基因组组织,染色体定位和表达模式。牛PPARGC1A基因组织在13个外显子中,包含6,261 bp,并在大量组织中以不同水平表达。牛PPARGC1A cDNA和蛋白质序列与其来自人类,大鼠和小鼠的直向同源物显示出实质相似性(92–95%)。在QTL上具有不同基因型的奶牛中,PPARGC1A基因的编码序列,外显子/内含子边界,5'-和3'-非翻译区以及启动子区的多态性筛查,以及多品种组揭示了总共11个多态位点。在主要奶牛种群中观察到PPARGC1A基因内含子9中的SNP与乳脂产量之间存在显着关联,这表明PPARGC1A基因可能参与了BTA6上乳脂合成的QTL的遗传变异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号