Strain Information | |
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Image | |
BRC No. | RBRC01386 |
Type | Transgene |
Species | Mus musculus |
Strain name | B6;FVB-Tg(ACTA1-cre)AMcle/Rbrc |
Former Common name | Transgenic mouse, MuCre-A |
H-2 Haplotype | |
ES Cell line | |
Background strain | |
Appearance | |
Strain development | The expression construct was created by cloning cDNAs encoding the selected genes and the promoter into a plasmid vector. After verification of the construct by nucleotide sequencing, the transcriptional unit was cleaved out with restriction enzymes, purified with biochemical method and used for microinjection. The offspring were initially examined by PCR genotyping. The in vivo expression was checked by chemical LacZ activity staining after crossing with a Cre-expression detection mouse line (Rosa26-Floxed LacZ). The entire process took from 1999 to 2003. |
Strain description | MuCreA contains a transcriptional unit consisting of a muscle-specific promoter (alpha-actin promoter) and Cre recombinase gene. This can be used to make an inducible knock-out by crossing with the other GM mice that have Floxed genes. MuCreA is a driver mouse that can remove Floxed genes only in skeletal muscle, but the genes to be removed are marked in the partner lines. |
Colony maintenance | |
References | Int. J. Biol. Sci., 20;6(6):546-555 (2010). 20877696 |
Health Report | |
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Examination Date / Room / Rack | 2024/03/11Room:3-2Rack:D 2023/12/11Room:3-2Rack:D 2023/09/11Room:3-2Rack:D 2023/06/13Room:3-2Rack:D 2023/03/13Room:3-2Rack:D 2022/12/12Room:3-2Rack:D 2022/09/12Room:3-2Rack:D 2022/06/13Room:3-2Rack:D |
Gene | |
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Gene info | Gene symbolGene nameChr.Allele symbolAllele nameCommon namesPromoter crePhage P1 Cre recombinaseUNcre<Tg(ACTA1-cre)AMcle>transgene insertion A, Ian S. McLennanhuman alpha actin promoter Gene symbolGene nameChr.Allele symbolAllele nameCommon namesPromoter SV40 polyA signalUN |
Ordering Information | |
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供与核酸 | human alpha skeletal muscle actin promoter, phage P1 Cre recombinase, SV40 poly A signal |
Research application | Cre/loxP system |
提供条件 | 条件を付加する。 研究成果の公表にあたって寄託者の指定する文献を引用する。Int. J. Biol. Sci., 20;6(6):546-555 (2010). |
Depositor | 小石 恭子(University of Otago) |
Strain Status | 生体 凍結胚 凍結精子 |
Strain Availability | 凍結精子を1ヶ月以内に提供可能 凍結胚を1ヶ月以内に提供可能 生体マウスを1~3ヶ月以内に提供可能 |
Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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Azhar M, Wang PY, Frugier T, Koishi K, Deng C, Noakes PG, McLennan IS. Myocardial deletion of Smad4 using a novel α skeletal muscle actin Cre recombinase transgenic mouse causes misalignment of the cardiac outflow tract. Int J Biol Sci 6(6) 546-55(2010) 20877696 Fujimoto M, Kitamura H. Application of the colorimetric loop-mediated isothermal amplification (LAMP) technique for genotyping Cre-driver mice. J Vet Med Sci 84(4) 507-510(2022) 35228407 Uruno A, Yagishita Y, Katsuoka F, Kitajima Y, Nunomiya A, Nagatomi R, Pi J, Biswal SS, Yamamoto M. Nrf2-Mediated Regulation of Skeletal Muscle Glycogen Metabolism. Mol Cell Biol 36(11) 1655-72(2016) 27044864 Uruno A, Furusawa Y, Yagishita Y, Fukutomi T, Muramatsu H, Negishi T, Sugawara A, Kensler TW, Yamamoto M. The Keap1-Nrf2 system prevents onset of diabetes mellitus. Mol Cell Biol 33(15) 2996-3010(2013) 23716596 |