B6.Cg-Gnb4tm1.1(cre/ERT2)Hze/J

Cat. No.: CEMM-07250779

Common Name: Gnb4-IRES2-CreERT2-D knock-in
Gnb4-IRES2-CreERT2-D knock-in mice express tamoxifen-inducible Cre recombinase from the endogenous guanine nucleotide binding protein (G protein) beta 4 promoter/enhancer elements. When induced, CreERT2 expression/activity is enriched in restricted populations within cortical subplate (claustrum and endopiriform nucleus) and layers 5/6 of lateral areas of cortex. Expression is also observed in some vascular cells. These mice may be used to generate conditional mutations for studying gain-or-loss of function and/or fate mapping related to this G protein.
Inquiry
Status Live Mouse
Frozen Embryo
Age 4 weeks
12 weeks
Customized Age
Sex Male
Female
GENETICS
Allele Symbol
Gnb4tm1.1(cre/ERT2)Hze
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Allele Name
targeted mutation 1.1
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Allele Attributes
Recombinase-expressing; Inducible
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Gene Symbol
Gnb4
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Gene Name
guanine nucleotide binding protein (G protein)
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Chromosome
3
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Expressed Genes
cre/ERT2, Cre recombinase and estrogen receptor 1 (human) fusion gene
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MGI Accession ID show more close
Site of Expression
CreERT2 is inducible following Tamoxifen administration, and When bred with mice containing lox-flanked sequences, Tamoxifen-inducible Cre-mediated recombination will result in deletion of floxed sequences in Gnb4-expressing cells of the offspring such as in the cortex and some vascular cells.
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Strain of Origin
(129S6/SvEvTac x C57BL/6NCrl)F1
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Molecular Note
The targeting vector contained, from 5' to 3', a partial Gnb4 sequence spanning intron 6 through intron 9 and part of exon 10 (including the endogenous stop codon), an internal ribosome entry site 2 (IRES2) sequence (allows translation initiation in the middle of an mRNA sequence), a CreERT2 fusion gene (Cre-ERT2; Cre recombinase fused to a G400V/M543A/L544A triple mutation of the human estrogen receptor ligand binding domain), a bovine growth hormone polyA sequence, an AttB site, a PGK promoter-Neomycin resistance gene-PGK polyA cassette, an frt5 site, an mRNA splice acceptor sequence, the 3' portion of the hygromycin gene (Hygro2) with SV40 polyA signal, and an AttP site. This targeting vector was electroporated into G4 ES cells. Correctly targeted ES cells were injected into recipient blastocysts. The resulting chimeric animals were bred to PhiC31-expressing mice to delete the AttB/AttP-flanked sequences and replace it with the recombined AttB/AttP site (AttL). The tamoxifen-inducible Cre recombinase activity is enriched in restricted populations within cortical subplate (claustrum and endopiriform nucleus) and layers 5/6 of lateral areas of cortex. Expression is also observed in some vascular cells.
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HUSBANDRY
Suggested Controls
C57BL/6J
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Breeding Considerations
When maintaining a live colony, heterozygous mice may be bred together, to wildtype mice from the colony or to C57BL/6J inbred mice. it has not been attempted to make this strain homozygous.
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Breeding Strategy
Wild-type x Heterozygote; Heterozygote x Wild-type
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For Research Use Only.
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