首页> 美国卫生研究院文献>Springer Open Choice >Evaluation of the Serotonergic Genes htr1A htr1B htr2A and slc6A4 in Aggressive Behavior of Golden Retriever Dogs
【2h】

Evaluation of the Serotonergic Genes htr1A htr1B htr2A and slc6A4 in Aggressive Behavior of Golden Retriever Dogs

机译:血清素能基因htr1Ahtr1Bhtr2A和slc6A4在金毛犬攻击行为中的评估

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Aggressive behavior displays a high heritability in our study group of Golden Retriever dogs. Alterations in brain serotonin metabolism have been described in aggressive dogs before. Here, we evaluate whether four genes of the canine serotonergic system, coding for the serotonin receptors 1A, 1B, and 2A, and the serotonin transporter, could play a major role in aggression in Golden Retrievers. We performed mutation screens, linkage analysis, an association study, and a quantitative genetic analysis. There was no systematic difference between the coding DNA sequence of the candidate genes in aggressive and non-aggressive Golden Retrievers. An affecteds-only parametric linkage analysis revealed no strong major locus effect on human-directed aggression related to the candidate genes. An analysis of 41 single nucleotide polymorphisms (SNPs) in the 1 Mb regions flanking the genes in 49 unrelated human-directed aggressive and 49 unrelated non-aggressive dogs did not show association of SNP alleles, genotypes, or haplotypes with aggression at the candidate loci. We completed our analyses with a study of the effect of variation in the candidate genes on a collection of aggression-related phenotypic measures. The effects of the candidate gene haplotypes were estimated using the Restricted Maximum Likelihood method, with the haplotypes included as fixed effects in a linear animal model. We observed no effect of the candidate gene haplotypes on a range of aggression-related phenotypes, thus extending our conclusions to several types of aggressive behavior. We conclude that it is unlikely that these genes play a major role in the variation in aggression in the Golden Retrievers that we studied. Smaller phenotypic effects of these loci could not be ruled out with our sample size.Electronic supplementary materialThe online version of this article (doi:10.1007/s10519-007-9179-7) contains supplementary material, which is available to authorized users.
机译:在我们的金毛犬研究小组中,攻击性行为显示出很高的遗传力。先前已经在攻击性犬中描述了脑5-羟色胺代谢的改变。在这里,我们评估犬血清素能系统的四个基因,它们编码5-羟色胺受体1A,1B和2A以及5-羟色胺转运蛋白,是否可能在金毛寻回犬的攻击中起主要作用。我们进行了突变筛选,连锁分析,关联研究和定量遗传分析。在攻击性和非攻击性金毛猎犬中,候选基因的编码DNA序列之间没有系统的差异。仅受影响的参数连锁分析显示,与候选基因相关的人类定向攻击没有强大的主要基因座效应。对49只无关的人类定向攻击性和49只无关的非攻击性狗的基因侧翼的1 Mb区中的41个单核苷酸多态性(SNP)的分析未显示SNP等位基因,基因型或单倍型与候选基因座上的攻击性相关。我们通过研究候选基因变异对一系列侵略相关表型的影响来完成分析。使用限制性最大似然法估计候选基因单倍型的作用,并将单倍型作为固定作用包括在线性动物模型中。我们没有观察到候选基因单倍型对一系列与攻击相关的表型的影响,因此将我们的结论扩展到了几种攻击行为类型。我们得出的结论是,这些基因不太可能在我们研究的金毛寻回犬的攻击变异中起主要作用。我们的样本量不能排除这些基因座的较小表型效应。电子补充材料本文的在线版本(doi:10.1007 / s10519-007-9179-7)包含补充材料,授权用户可以使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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