The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12

被引:28
作者
Achilli, F
Boyle, S
Kieran, D
Chia, R
Hafezparast, M
Martin, JE
Schiavo, G
Greensmith, L
Bickmore, W
Fisher, EMC
机构
[1] Inst Neurol, Dept Neurodegenerat Dis, London WC1N 3BG, England
[2] Inst Neurol, Sorbell Dept Motor Sci & Movement Disorders, London WC1N 3BG, England
[3] MRC, Human Genet Unit, Chromosome Biol Sect, Edinburgh, Midlothian, Scotland
[4] Univ Sussex, Sch Life Sci, Dept Biochem, Brighton, E Sussex, England
[5] Queen Mary Univ London, Royal London Hosp, Dept Histopathol, London, England
[6] Canc Res UK London Res Inst, Mol Neuropathobiol Lab, London, England
来源
AMYOTROPHIC LATERAL SCLEROSIS | 2005年 / 6卷 / 02期
基金
英国医学研究理事会;
关键词
amyotrophic lateral sclerosis; SOD1; G93A; transgenic; Loa; mouse model;
D O I
10.1080/14660820510035351
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The SOD1G93A transgenic mouse strain which carries a human mutant Cu/Zn superoxide dismutase transgene array is a widely studied model of amyotrophic lateral sclerosis. These mice have been used in many breeding experiments to look for interactions with other loci, including transgenic and gene targeted mutations. Therefore, we decided to map the site of the transgene insertion as this may affect the outcome of such breeding experiments. In a fluorescence in situ hybridization experiment we determined that the SOD1G93A transgene insertion site lies on distal mouse chromosome 12. This chromosome also carries the 'Legs at odd angles' locus, which is an entirely unrelated mutation in the dynein heavy chain gene that we have been studying. We have analysed data from a SOD1G93A x Loa cross and determined that the site of the transgene insertion lies proximal of the dynein heavy chain gene on mouse chromosome 12.
引用
收藏
页码:111 / 114
页数:4
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