Pdgfrbtm1.1(cre/ERT2)Csln
Targeted Allele Detail
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Symbol: |
Pdgfrbtm1.1(cre/ERT2)Csln |
Name: |
platelet derived growth factor receptor, beta polypeptide; targeted mutation 1.1, Chyuan-Sheng Lin |
MGI ID: |
MGI:5901894 |
Synonyms: |
PDGFRbata-P2A-CreERT2 |
Gene: |
Pdgfrb Location: Chr18:61178222-61218133 bp, + strand Genetic Position: Chr18, 34.41 cM
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Alliance: |
Pdgfrbtm1.1(cre/ERT2)Csln page
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Allele Type: |
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Targeted (Inducible, Recombinase) |
Inducer: |
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tamoxifen |
Mutation: |
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Insertion
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Pdgfrbtm1.1(cre/ERT2)Csln expression driven by
1 gene
Knock-in expression driven by:
Organism |
Driver Gene |
Note |
mouse |
Pdgfrb (MGI:97531) |
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Mutation details: A targeting vector was designed to replace the translation stop codon of the platelet derived growth factor receptor, beta polypeptide (Pdgfrb) gene with a creER fusion gene (a Cre recombinase fused to a human estrogen receptor ligand binding domain) followed by a frt-flanked neomycin resistance (neo) cassette. A viral P2A oligopeptide, from porcine teschovirus-1, was inserted upstream of the creER fusion gene to ribosomal skipping. The construct was electroporated into (C57BL/6J x 129S6/SvEvTac)F1-derived KV1 embryonic stem (ES) cells. Correctly targeted ES cells were injected into C57BL6/N blastocysts and resulting chimeric males were bred to Tg(ACTFLPe)9205Dym/J females to remove the neo cassette. These mice express Cre-ER protein in pericytes in the vasculature of organs including brain and retina. Restricted to the cytoplasm, Cre-ER can only gain access to the nuclear compartment after exposure to tamoxifen.
(J:263753)
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Activity: |
Tissue activity of this recombinase allele
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Driver:
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Pdgfrb
(mouse)
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Original: |
J:263753 Cuervo H, et al., PDGFRbeta-P2A-CreER(T2) mice: a genetic tool to target pericytes in angiogenesis. Angiogenesis. 2017 Nov;20(4):655-662 |
All: |
15 reference(s) |
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