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日本野生鼷鼠:新型疾病模型的丰富资源。

Japanese wild mice: a rich resource for new disease models.

机构信息

Saitama Cancer Center, Research Institute for Clinical Oncology, Kitaadachi, Saitama, Japan.

出版信息

Exp Anim. 2012;61(1):25-33. doi: 10.1538/expanim.61.25.

DOI:10.1538/expanim.61.25
PMID:22293669
Abstract

Breeding of fancy mice has been a tradition in Japan. Recent progress in animal science has shed a new light on Japanese wild-derived mice as tools for discovery of new disease models because these mice, Mus musculus molossinus, are genetically far remote from the majority of available laboratory mice. After decades of effort, five inbred strains of mice have been established from pairs of wild mice trapped in Tohoku, northeastern Japan, namely KOR1/Stm, KOR5/Stm, KOR7/Stm, AIZ/Stm, and MAE/Stm. They carried numerous mutations, leading to a variety of diseases. During the inbreeding of KOR1, the first spontaneous mutation was found in the Apoe (apolipoprotein E) gene, and the mutant was later designated as spontaneous hyperlipidemic (SHL). Thereafter, a number of other mutations were discovered among wild-derived inbred strains, including atopic dermatitis, microphthalmia, dominant white spots, sebaceous gland abnormalities, and audible song-like vocalization. Furthermore, to examine the possible effects of the genetic background for these mutant genes, sets of congenic strains were generated, in which the mutant gene was introduced into at least 3 different strains of laboratory mice, including BALB/c and C57BL/6. These congenic strains have now been established as novel disease models. These wild-derived inbred strains serve as a treasure trove for novel disease models. Most of them have been deposited in the Riken BioResource Center (BRC), and some are also available from commercial breeders.

摘要

在日本,培育花式老鼠一直是一种传统。动物科学的最新进展为日本野生来源的老鼠作为发现新疾病模型的工具提供了新的视角,因为这些老鼠,即 Mus musculus molossinus,在遗传上与大多数可用的实验鼠相差甚远。经过几十年的努力,已经从日本东北地区的东北地区捕获的一对野生老鼠中建立了五个近交系小鼠,即 KOR1/Stm、KOR5/Stm、KOR7/Stm、AIZ/Stm 和 MAE/Stm。它们携带了许多突变,导致了多种疾病。在 KOR1 的近交过程中,第一个自发突变出现在 Apoe(载脂蛋白 E)基因中,该突变体后来被命名为自发性高脂血症(SHL)。此后,在野生来源的近交系中发现了许多其他突变,包括特应性皮炎、小眼症、显性白色斑点、皮脂腺异常和可听见的类似歌声的发声。此外,为了研究这些突变基因的遗传背景的可能影响,还生成了一系列同基因系,其中突变基因被引入至少 3 种不同的实验鼠品系,包括 BALB/c 和 C57BL/6。这些同基因系现已被确立为新型疾病模型。这些野生来源的近交系是新型疾病模型的宝库。它们中的大多数已被存入 Riken 生物资源中心(BRC),有些也可从商业饲养者处获得。

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