首页> 外文期刊>Agricultural Sciences >Association of NOS3 and HIF1α gene polymorphisms with the susceptibility of broiler chickens to develop hypoxic pulmonary hypertension
【24h】

Association of NOS3 and HIF1α gene polymorphisms with the susceptibility of broiler chickens to develop hypoxic pulmonary hypertension

机译:NOS3和HIF1α基因多态性与肉鸡发生缺氧性肺动脉高压的相关性

获取原文
           

摘要

A genetic association between single nucleotide polymorphisms (SNPs) and pulmonary hypertension syndrome (PHS) was established in a commercial population of broiler chickens. The associated SNPs were found in the NOS3 and HIF1α genes (LOD > 6; p NOS3 gene interfere with its trans-activation and transcriptional activation activities under natural hypobaric hypoxia conditions and are located in a consensus sequence that is called the hypoxia response element (HRE). SNPs located in the HIF1α gene could act as alternative cryptic splicing sites in intron six, which may stimulate non-sense mediated early decay (NMD) of the primary transcript. A fragment of intron 3 of the EDN1 gene was also evaluated, but the polymorphisms found were not associated with PHS (lod 0.001). However, further studies on the regulatory transcription sequences of EDN1 are recommended. The findings of this study indicate that intronic sequences should be included when searching for polymorphisms that produce physiological changes. Introns have transcriptional regulatory sequences or post-transcriptional control signals, which are known as cis- and trans-activation regulatory elements and are able to alter the physiological processes of hypoxia adaptation when modified. Based on these findings, it can be concluded that the inheritance pattern of PHS is autosomal overdominant and has deleterious effects that are characterized by higher penetrance in heterozygous than in homozygous animals, which prevent broiler chickens from being able to adapt to high altitudes.
机译:在商业肉鸡群中建立了单核苷酸多态性(SNP)与肺动脉高压综合征(PHS)之间的遗传关联。在自然低压缺氧条件下,在NOS3和HIF1α基因中发现了相关的SNP(LOD> 6; p NOS3基因干扰其反式激活和转录激活活性,位于一个称为缺氧反应元件(HRE)的共有序列中。 )。位于HIF1α基因中的SNPs可以作为内含子6中的选择性密码子剪接位点,可能刺激初级转录本的无义介导的早期衰变(NMD)。还对EDN1基因的内含子3的片段进行了评估,但所发现的多态性与PHS无关(第0.001位),但建议对EDN1的调控转录序列进行进一步研究,该结果表明,在寻找可引起生理变化的多态性时,应包括内含子序列。转录调控序列或转录后控制信号,称为顺式和反式激活调控元件,修改后能够改变低氧适应的生理过程。根据这些发现,可以得出结论,PHS的遗传模式是常染色体显性遗传,并且具有有害作用,其特征在于杂合子中的渗透率高于纯合子动物中的渗透率,这阻止了肉鸡适应高海拔地区。

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