B6.Cg-Igs7tm148.1(tetO-GCaMP6f, CAG-tTA2)Hze/J

Cat. No.: CEMM-07250794

Common Name: Ai148(TIT2L-GC6f-ICL-tTA2)-D (or Ai148D)
Ai148(TIT2L-GC6f-ICL-tTA2)-D (also called Ai148D) mice are a Cre-dependent, Tet-controllable, fluorescent calcium-indicator tool strain, created by targeted insertion at the Igs7 locus (TIGRE; an intergenic region on mouse chromosome 9 that allows reporter expression to be tightly regulated). Exposure to Cre recombinase removes both STOP cassettes, resulting in expression of tTA2 and GCaMP6f (a bright EGFP fluorescent calcium indicator of single neuronal action potentials with fast response kinetics). GCaMP6f expression may then be diminished/eliminated by doxycycline.
Inquiry
Status Live Mouse
Frozen Embryo
Age 4 weeks
12 weeks
Customized Age
Sex Male
Female
GENETICS
Allele Symbol
Igs7tm148.1(tetO-GCaMP6f,CAG-tTA2)Hze
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Allele Name
targeted mutation 148.1
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Allele Attributes
Conditional ready (e.g. floxed); Reporter; Inducible; Transactivator
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Gene Symbol
Igs7
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Gene Name
intergenic site 7
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Chromosome
9
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Expressed Genes
GCaMP, Genetically encoded calcium indicator; tTA, tetracycline-controlled transactivator, E. coli
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MGI Accession ID show more close
Site of Expression
When these mice are bred with Cre-driver lines, baseline EGFP fluorescence is observed in the absence of calcium binding and robust fluorescence is observed after calcium binding. Upon administration of dox, EGFP fluorescence is eventually completely suppressed.
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Strain of Origin
(129S6/SvEvTac x C57BL/6NCrl)F1
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Molecular Note
The replacement vector was designed with (from 5' to 3') an FRT3 site, two copies of chicken beta-globin HS4 insulator element, a Tet response element/promoter (TRE2), a loxP-flanked STOP cassette, a GCaMP6 fast variant calcium indicator sequence (GCaMP6f; details below), a WPRE, a BGH polyA, two copies of chicken beta-globin HS4 insulator element, a CMV-IE enhancer/chicken beta-actin/rabbit beta-globin hybrid promoter (CAG; from pCAGGS), a lox2272-flanked STOP cassette, a synthetic modified tetracycline-regulated transactivator gene (tTA2S), a WPRE, a BGH polyA, an AttB site, a PGK-5'hygro cassette, an RNA splice donor and a FRT5 site. Embryonic stem cells previously targeted with FRT3::AttB::PGK-neoR-polyA::FRT5::splice acceptor::3'hygro cassette::SV40 polyA:AttP in TIGRE, were re-transfected with the replacement vector and Flp recombinase vector for recombinase-mediated cassette exchange (RCME). PhiC31-mediated recombination removed the AttB/AttP-flanked sequence (PGK-Neo-polyA::frt5::RNA splice acceptor::3'hygro-polyA) and replaced it with the recombined AttB/AttP site (AttL). The GCaMP6f fusion gene has a chicken smooth muscle M13 fragment of myosin light chain kinase, a circularly permutated EGFP, and a rat calmodulin DNA fragment. The GCaMP6 fast variant calcium indicator (GCaMP6f) is a detector of single neuronal action potentials with fast response kinetics, and is an improved version of GCaMP5G. Compared to GCaMP6s, GCaMP6f has faster response but is less sensitive and faster to decay. In the absence of calcium binding, dim EGFP fluorescence is expected as there is a pore from the outside of its barrel into the chromophore. Upon calcium binding, this pore becomes occupied and fluorescence is inCreased.
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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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