Strain Data Sheet

RBRC05821

Strain Information

Image
BRC No.RBRC05821
TypeTargeted MutationCartagena
SpeciesMus musculus
Strain nameB6.Cg-Camk2a<tm1.1Oyam>
Former Common nameB6-CaMKII alpha (K42R), B6-Camk2a KI/K42R
H-2 Haplotype
ES Cell lineTT2 [(C57BL/6NCrlj x CBA/JNCrlj)F1]
Background strain
Appearance
Strain developmentDeveloped by Yoko Yamagata and Yuchio Yanagawa, National Institute for Physiological Sciences in 2003. Derived from TT2 ES cell line (B6CBAF1 derived). The PGK-neo cassette was removed by transient expression of cre recombinase in ES cells. C57BL/6 background (RBRC05821), ICR mixed background (RBRC05636).
Strain descriptionCamk2a/K42R knock-in mice. Ca<2+>/calmodulin-dependent protein kinase IIalpha (CaMKII alpha/ Camk2a) is an enzyme that adds phosphates to a variety of protein substrates to modify their functions. CaMKIIalpha is especially enriched in the hippocampus, and is believed to be an essential mediator of activity-dependent synaptic plasticity and memory functions. We generated a novel kinase-dead knock-in mouse of the CaMKII alpha gene that completely and exclusively lacks its kinase activity by introducing a point mutation (K42R) that prevents ATP binding necessary for phosphorylation reaction. Both heterozygous and homozygous mice are hyperactive, but otherwise indistinguishable from wild-type mice. They are fertile and without any obvious neurological symptoms, except for sporadic observation of mild limbic seizure. Homozygous mice are severely impaired with hippocampal synaptic plasticity and hippocampus-dependent memory formation. Suitable for studies of the mechanisms of LTP and learning and memory, and as a memory-deficit animal model.
Colony maintenanceBack crossed to C57BL/6NCrlCrlj for more than 20 generations.
References
Kinase-dead knock-in mouse reveals an essential role of kinase activity of Ca2+/calmodulin-dependent protein kinase IIalpha in dendritic spine enlargement, long-term potentiation, and learning.
Yamagata Y, Kobayashi S, Umeda T, Inoue A, Sakagami H, Fukaya M, Watanabe M, Hatanaka N, Totsuka M, Yagi T, Obata K, Imoto K, Yanagawa Y, Manabe T, Okabe S
J. Neurosci., 29, 7607-7618 (2009). 19515929

Health Report

Examination Date / Room / Rack

Gene

Gene SymbolGene NameChr.Allele SymbolAllele NameCommon NamesPromoterDiseases Related to This Gene
Camk2a
MGI:88256
calcium/calmodulin-dependent protein kinase II alpha18Camk2a<tm1.1Oyam>
MGI:3849851
targeted mutation 1.1, Yoko Yamagata
  • intellectual disability, autosomal dominant 53(MedGEN)

  • intellectual disability, autosomal recessive 63(MedGEN)
  • loxP phage P1 loxP18loxP

    Phenotype

    Annotation by Mammalian phenotyhpe ontology
  • abnormal avoidance learning behavior(MP:0001462)

  • abnormal circadian behavior(MP:0020467)

  • abnormal cued conditioning behavior(MP:0001454)

  • abnormal neuron morphology(MP:0002882)

  • abnormal short-term spatial reference memory(MP:0008431)
  • more 6 phenotypes
  • abnormal spatial learning(MP:0001463)

  • decreased survivor rate(MP:0008770)

  • hyperactivity(MP:0001399)

  • premature death(MP:0002083)

  • reduced long-term potentiation(MP:0001473)

  • sporadic seizures(MP:0000951)
  • Detailed phenotype data

    Ordering Information

    Donor DNAP1 Phage loxP site, mouse Camk2a genomic DNA
    Research applicationCre/loxP system
    Neurobiology Research
    Specific Term and ConditionsIn publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. J. Neurosci., 29, 7607-7618 (2009).
    DepositorYoko Yamagata (National Institute for Physiological Sciences)
    Strain Statusan icon for Frozen spermFrozen sperm
    Strain AvailabilityLive mouse (more than 6 months)
    Additional Info.Necessary documents for ordering:
    1. Order form (Japanese / English)
    2. Category I MTA: MTA for distribution with RIKEN BRC (Japanese / English)
    3. Acceptance of responsibility for living modified organism (Japanese / English)

    Genotyping protocol -PCR-

    BRC mice in Publications

    No Data