首页> 美国卫生研究院文献>Genome Research >Vestibular Dysfunction in the Epistatic circler Mouse Is Caused by Phenotypic Interaction of One Recessive Gene and Three Modifier Genes
【2h】

Vestibular Dysfunction in the Epistatic circler Mouse Is Caused by Phenotypic Interaction of One Recessive Gene and Three Modifier Genes

机译:一个隐性基因和三个修饰基因的表型相互作用导致上环圈鼠小鼠前庭功能障碍

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

Vestibular dysfunction is a frequent clinical problem, leading to dizziness and imbalance. Genes play an important role in its etiology, but the genetics are complex and poorly understood. In this study we have analyzed the complex inheritance pattern in the Epistatic circler mouse, which shows circling behavior indicative of vestibular dysfunction in the mouse. This phenotype exists in a proportion of the F2-generation from an intercross between C57L/J and SWR/J mouse strains. Genetic investigation indicates that the circling behavior is caused by a major recessively inherited gene derived from the SWR/J strain (the Ecs-gene) in combination with at least three different modifier genes derived from C57L/J (the Ecl-genes). Genetic mapping made it possible to localize the Ecs-gene to chromosome 14 and the Ecl-genes to chromosome 3, 4, and 13. This study illustrates the feasibility of identifying genes for multifactorial traits in mice.
机译:前庭功能障碍是常见的临床问题,导致头晕和不平衡。基因在其病因学中起着重要的作用,但是遗传学是复杂的,人们对此知之甚少。在这项研究中,我们分析了上位环行小鼠的复杂遗传模式,该模式显示了指示小鼠前庭功能障碍的盘旋行为。这种表型存在于C57L / J和SWR / J小鼠品系之间的交配中,是F2代的一部分。遗传研究表明,这种盘旋行为是由SWR / J株的一个主要隐性遗传基因(Ecs基因)与至少三个C57L / J的修饰基因(Ecl基因)结合引起的。遗传图谱使将Ecs基因定位在14号染色体上,并将Ecl基因定位在3号,4号和13号染色体上成为可能。

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