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首页> 外文期刊>Hearing Research: An International Journal >Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice
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Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice

机译:遗传背景对小鼠Cdh23变体相关的年龄相关性听力损失的影响

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摘要

Inbred strain variants of the Cdh23 gene have been shown to influence the onset and progression of age-related hearing loss (AHL) in mice. In linkage backcrosses, the recessive Cdh23 allele (ahl) of the C57BL/6J strain, when homozygous, confers increased susceptibility to AHL, while the dominant allele (Ahl+) of the CBA/CaJ strain confers resistance. To determine the isolated effects of these alleles on different strain backgrounds, we produced the reciprocal congenic strains B6.CBACa-Cdh23 Ahl+ and CBACa.B6-Cdh23 ahl and tested 15-30 mice from each for hearing loss progression. ABR thresholds for 8kHz, 16kHz, and 32kHz pure-tone stimuli were measured at 3, 6, 9, 12, 15 and 18 months of age and compared with age-matched mice of the C57BL/6J and CBA/CaJ parental strains. Mice of the C57BL/6N strain, which is the source of embryonic stem cells for the large International Knockout Mouse Consortium, were also tested for comparisons with C57BL/6J mice. Mice of the C57BL/6J and C57BL/6N strains exhibited identical hearing loss profiles: their 32kHz ABR thresholds were significantly higher than those of CBA/CaJ and congenic strain mice by 6 months of age, and their 16kHz thresholds were significantly higher by 12 months. Thresholds of the CBA/CaJ, the B6.CBACa-Cdh23 Ahl+, and the CBACa.B6-Cdh23 ahl strain mice differed little from one another and only slightly increased throughout the 18-month test period. Hearing loss, which corresponded well with cochlear hair cell loss, was most profound in the C57BL/6J and C57BL/6NJ strains. These results indicate that the CBA/CaJ-derived Cdh23 Ahl+ allele dramatically lessens hearing loss and hair cell death in an otherwise C57BL/6J genetic background, but that the C57BL/6J-derived Cdh23 ahl allele has little effect on hearing loss in an otherwise CBA/CaJ background. We conclude that although Cdh23 ahl homozygosity is necessary, it is not by itself sufficient to account for the accelerated hearing loss of C57BL/6J mice.
机译:已显示Cdh23基因的近交菌株变异会影响小鼠与年龄有关的听力损失(AHL)的发作和进展。在连锁回交中,当纯合时,C57BL / 6J菌株的隐性Cdh23等位基因(ahl)赋予对AHL的敏感性增加,而CBA / CaJ菌株的显性等位基因(Ahl +)赋予抗性。为了确定这些等位基因对不同菌株背景的分离作用,我们制备了互基因同系菌株B6.CBACa-Cdh23 Ahl +和CBACa.B6-Cdh23 ahl,并从每只15-30只小鼠中测试了听力损失的进展。在3、6、9、12、15和18个月大时测量8kHz,16kHz和32kHz纯音刺激的ABR阈值,并与C57BL / 6J和CBA / CaJ亲本菌株的年龄匹配小鼠进行比较。还测试了C57BL / 6N小鼠的小鼠,该小鼠是大型国际基因敲除小鼠协会的胚胎干细胞来源,用于与C57BL / 6J小鼠进行比较。 C57BL / 6J和C57BL / 6N品系的小鼠表现出相同的听力损失曲线:到6个月大时,它们的32kHz ABR阈值显着高于CBA / CaJ和同基因品系小鼠,而到12个月时,其16kHz阈值显着更高。 CBA / CaJ,B6.CBACa-Cdh23 Ahl +和CBACa.B6-Cdh23 ahl品系小鼠的阈值彼此之间几乎没有差异,并且在整个18个月的测试期间仅略有增加。与C57BL / 6J和C57BL / 6NJ菌株相比,听力损失与耳蜗毛细胞损失非常吻合。这些结果表明,在其他C57BL / 6J遗传背景下,CBA / CaJ衍生的Cdh23 Ahl +等位基因显着减少了听力损失和毛细胞死亡,而在其他情况下,C57BL / 6J衍生的Cdh23 ahl等位基因对听力损失的影响很小CBA / CaJ背景。我们得出结论,尽管Cdh23 ahl纯合性是必要的,但仅凭其本身不足以解决C57BL / 6J小鼠加速听力丧失的问题。

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