- increased circulating alanine transaminase level / IMPC
- enlarged spleen / IMPC
- increased circulating creatine kinase level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased circulating fructosamine level / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased fasting circulating glucose level / IMPC
- decreased exploration in new environment / IMPC
B6.129-Prkaa2tm1Vio/Orl
| Status | Available to order |
| EMMA ID | EM:01420 |
| Citation information | RRID:IMSR_EM:01420 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | B6.129-Prkaa2tm1Vio/Orl |
| Alternative name | AMPKalpha2_floxed |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Prkaa2tm1Vio |
| Gene/Transgene symbol | Prkaa2 |
Information from provider
| Provider | Sophie Vaulont |
| Provider affiliation | INSERMU567, CNRS UMR8401, universite Paris 5, Institut Cochin |
| Genetic information | Protein kinase, AMP-activated, alpha 2 (Prkaa2 or AMPK alpha2) locus. A mouse 129 strain lambda genomic library (Stratagene) was screened with a AMPK alpha2 500-bp fragment, made by reverse-transcription polymerase chain reaction on liver mRNA. This fragment contains the exon encoding the C-terminus part of AMPK alpha2 catalytic domain (exon C9). To introduce a loxP site, a double-stranded oligonucleotide (C-loxP-HindIII-SphI), was cloned 300 bp upstream of exon C. Embryonic stem cells (MPI) were electroporated with the linearized targeting construct and selected; clones heterozygous for the floxed allele were injected into C57BL/6 blastocysts. Chimeric male mice were crossed with C57BL/6 female mice to generate heterozygous floxed/wild-type allele mice, and heterozygous mice were mated to generate homozygous mice. |
| Phenotypic information | No apparent defect. |
| Breeding history | AMPKalpha2_floxed(+/-) mice were backcrossed 6 times to C57BL/6J background at the CDTA germ-free animal house in Orleans. |
| References |
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Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- increased circulating free fatty acid level / MGI
- hyperglycemia / MGI
- abnormal glucose homeostasis / MGI
- decreased circulating insulin level / MGI
- decreased insulin secretion / MGI
- abnormal muscle cell glucose uptake / MGI
- abnormal sympathetic nervous system physiology / MGI
- impaired glucose tolerance / MGI
- insulin resistance / MGI
- homeostasis/metabolism phenotype / MGI
- abnormal glycogen homeostasis / MGI
- decreased glycogen level / MGI
- decreased circulating leptin level / MGI
- abnormal urine catecholamine level / MGI
Literature references
- The AMP-activated protein kinase alpha2 catalytic subunit controls whole-body insulin sensitivity.;Viollet Benoit, Andreelli Fabrizio, Jørgensen Sebastian B, Perrin Christophe, Geloen Alain, Flamez Daisy, Mu James, Lenzner Claudia, Baud Olivier, Bennoun Myriam, Gomas Emmanuel, Nicolas Gaël, Wojtaszewski Jørgen F P, Kahn Axel, Carling David, Schuit Frans C, Birnbaum Morris J, Richter Erik A, Burcelin Rémy, Vaulont Sophie, ;2003;The Journal of clinical investigation;111;91-8; 12511592
- Cre-mediated germline mosaicism: a method allowing rapid generation of several alleles of a target gene.;Holzenberger M, Lenzner C, Leneuve P, Zaoui R, Hamard G, Vaulont S, Bouc Y L, ;2000;Nucleic acids research;28;E92; 11058142
- A tamoxifen-inducible chimeric Cre recombinase specifically effective in the fetal and adult mouse liver.;Tannour-Louet Mounia, Porteu Arlette, Vaulont Sophie, Kahn Axel, Vasseur-Cognet Mireille, ;2002;Hepatology (Baltimore, Md.);35;1072-81; 11981757
- Endothelial AMP-Activated Kinase α1 Phosphorylates eNOS on Thr495 and Decreases Endothelial NO Formation.;Zippel Nina, Loot Annemarieke E, Stingl Heike, Randriamboavonjy Voahanginirina, Fleming Ingrid, Fisslthaler Beate, ;2018;International journal of molecular sciences;19;; 30217073
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