Genetic mapping of the rat mutation creeping and evaluation of its positional candidate gene reelin

被引:7
作者
Yokoi, N
Shimizu, S
Ishibashi, K
Kitada, K
Iwama, H
Namae, M
Sugawara, M
Serikawa, T
Komeda, K [1 ]
机构
[1] Tokyo Med Univ, Div Lab Anim Sci, Ctr Anim Res, Shinjuku Ku, Tokyo 1608402, Japan
[2] Chiba Univ, Sch Med, Dept Med Genet Novo Nordisk Pharma, Chuo Ku, Chiba 2608670, Japan
[3] Kyoto Univ, Inst Lab Anim, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
[4] Nippon Vet & Anim Sci Univ, Dept Anim Biochem, Musashino, Tokyo 1808602, Japan
[5] Daiichi Pharmaceut Co Ltd, Expt Technol Res Ctr, Edogawa Ku, Tokyo 1348630, Japan
关键词
D O I
10.1007/s003350010022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously described a rat autosomal recessive mutation, creeping (cre), causing severe ataxia and disarrangement of neuronal cells in the central nervous system. The mutant strain has recently been successfully inbred, named Komeda Zucker creeping (KZC) rat. In the present study, we have performed a genetic analysis of the creeping mutation, and mapped it to rat Chromosome (Chr) 4. Comparative mapping, together with the similarity of the phenotype, suggested that the creeping mutation is homologous to the mouse reeler mutation. In fact, reelin expression was markedly reduced in the homozygous mutant (cre/cre) animals compared with the normal littermates. Thus, the KZC rat should become a useful biological model with a novel mutation in the reelin gene.
引用
收藏
页码:111 / 114
页数:4
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