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 crossing the mice with two Cre-reporter lines. |
Strain description | MuCreA contains a transcriptional unit consisting of a muscle-specific promoter (alpha-actin promoter) and Cre recombinase gene. The mouse is used to make myogenic-specific knock-outs by crossing with mice that have a floxed gene. The MuCreA produces rapid and early cleavage of floxed genes from all differentiated myogenic cells, including cardiac myocytes and skeletal myotubes. |
Colony maintenance | |
References | Myocardial deletion of Smad4 using a novel alpha skeletal muscle actin Cre recombinase transgenic mouse causes misalignment of the cardiac outflow tract. Azhar M, Wang P Y, Frugier T, Koishi K, Deng C, Noakes P G, McLennan I S Int. J. Biol. Sci., 20;6(6):546-555 (2010). 20877696 |
Health Report | |
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Examination Date / Room / Rack | 2024/12/09Room:3-2Rack:DSentinel mouse program 2024/09/09Room:3-2Rack:DSentinel mouse program 2024/06/10Room:3-2Rack:DSentinel mouse program 2024/03/11Room:3-2Rack:DSentinel mouse program 2023/12/11Room:3-2Rack:DSentinel mouse program 2023/09/11Room:3-2Rack:DSentinel mouse program 2023/06/13Room:3-2Rack:DSentinel mouse program |
Gene | |||||||
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Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
cre | Phage P1 Cre recombinase | UN | cre<Tg(ACTA1-cre)AMcle> MGI:4833970 | transgene insertion A, Ian S. McLennan | human alpha actin promoter | ||
SV40 polyA signal | UN |
Phenotype | |
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Annotation by Mammalian phenotyhpe ontology | |
Detailed phenotype data |
Ordering Information | |
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Donor DNA | human alpha skeletal muscle actin promoter, phage P1 Cre recombinase, SV40 poly A signal |
Research application | Cre/loxP system |
Specific Term and Conditions | In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. Int. J. Biol. Sci., 20;6(6):546-555 (2010). |
Depositor | Kyoko Koishi (University of Otago) |
Strain Status | ![]() ![]() ![]() |
Strain Availability | Cryopreserved sperm (within 1 month) Cryopreserved embryos (within 1 month) Live mouse (3 to 6 months) |
Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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Nakatsu Y, Matsunaga Y, Nakanishi M, Yamamotoya T, Sano T, Kanematsu T, Asano T. Prolyl isomerase Pin1 in skeletal muscles contributes to systemic energy metabolism and exercise capacity through regulating SERCA activity. Biochem Biophys Res Commun 715 150001(2024) 38676996 |
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 |
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 |