Kaneko Yui, Tomiyama Kayo, Yasuda Masahiko, Komaki Yuji, Ogura Tomoyuki, Takahashi Riichi, Yamamoto Masafumi
Central Institute for Experimental Medicine and Life Science, 3-25-12 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Exp Anim. 2025 Jan 10;74(1):122-131. doi: 10.1538/expanim.24-0045. Epub 2024 Sep 11.
Here, we report the identification of causative genes for limb-shortening in individuals repeatedly found in a population of severely immunodeficient NOG mice maintained via sibling mating. First, we conducted a pedigree survey to determine whether limb-shortening was a recessive genetic trait and then identified it using a crossing test. Simultaneously, the symptoms were identified in detail using pathological analysis. Accordingly, a mouse strain exhibiting a recessive trait caused by a single gene trait and similar symptoms was identified, suggesting growth differentiation factor 5 (Gdf5) as a causative gene. Genome walking via PCR and sequence analysis of Gdf5 revealed a deletion of approximately 1.1 kb from the latter half of exon 2 of Gdf5. Furthermore, we established NOG-Gdf5 by removing other modified genes and confirmed that the inheritance pattern was reconfirmed semi-dominant. In recent years, regenerative medicine research using immunodeficient mice has been actively conducted, and this murine strain is expected to contribute to niche stem cell analysis and transplantation research.
在此,我们报告了在通过同胞交配维持的严重免疫缺陷NOG小鼠群体中反复发现的个体肢体缩短致病基因的鉴定情况。首先,我们进行了系谱调查,以确定肢体缩短是否为隐性遗传性状,然后通过杂交试验对其进行鉴定。同时,使用病理分析详细鉴定了症状。据此,鉴定出一种由单基因性状引起的具有隐性性状和类似症状的小鼠品系,提示生长分化因子5(Gdf5)为致病基因。通过PCR进行基因组步移和对Gdf5的序列分析发现,Gdf5外显子2后半部分缺失了约1.1 kb。此外,我们通过去除其他修饰基因建立了NOG-Gdf5,并证实其遗传模式为半显性。近年来,利用免疫缺陷小鼠进行的再生医学研究一直在积极开展,预计该小鼠品系将有助于生态位干细胞分析和移植研究。