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| These Ple151-EGFP;mEMS1615 mice have the Ple151-EGFP transgene targeted as a single copy "knockin" into the upstream region of hypoxanthine guanine phosphoribosyl transferase 1 (Hprt1) locus on the X chromosome. As the promoter/regulatory regions of the human oligodendrocyte transcription factor 1 (OLIG1) gene direct expression of enhanced green fluorescent protein (EGFP), these Ple151-EGFP;mEMS1615 mice may be useful in studying OLIG1-expressing cells in the brain and diseases affecting the brain. | |||||||||||||||||||
Former Names B6.129P2-Hprt1tm8(OLIG1-EGFP)Ems/J (Changed: 10-MAR-09 ) Type Congenic; Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Mating System Heterozygote x Inbred (Female x Male) 18-JUL-09 Species laboratory mouse Generation N4+ (17-JUL-09) Donating Investigator Elizabeth Simpson, University of British Columbia Description
These Ple151-EGFP;mEMS1615 mice have the Ple151-EGFP transgene targeted as a single copy "knockin" into the upstream region of hypoxanthine guanine phosphoribosyl transferase 1 (Hprt1) locus on the X chromosome. Heterozygous females and hemizygous males are viable and fertile, with the promoter/regulatory regions of the human oligodendrocyte transcription factor 1 (OLIG1) gene directing expression of enhanced green fluorescent protein (EGFP). These Ple151-EGFP;mEMS1615 mice may be useful in studying OLIG1-expressing cells in the brain and diseases affecting the brain.The donating investigator reports:
Positive EGFP immunoreactivity was detected across numerous brain regions. EGFP-positive cells show darker staining in the nucleus with a lighter staining halo of processes. In the brainstem, cortex and thalamus, numerous immunopositive profiles are detected while fewer profiles are seen in the olfactory bulb, striatum and cerebellum. In contrast to the predicted expression of OLIG1, the EGFP expression does not appear to be enriched in white matter tracts such as the corpus callosum.For more characterization information, see The Pleiades Promoter Project website (Ple151 Promoter (pEMS1172)).
These mice were created and deposited by The Pleiades Promoter Project (Centre for Molecular Medicine and Therapeutics, University of British Columbia); their goal is to generate 160 fully characterized, human DNA promoters of less than 4 kb (MiniPromoters) to drive gene expression in defined brain regions of therapeutic interest for studying disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease, Amyotrophic Lateral Sclerosis (Lou Gehrig's disease), Multiple Sclerosis, Spinocerebellar Ataxia, Depression, Autism, and Cancer.
Development
The Ple151-EGFP transgene (pEMS1172) was designed with a Ple151 minipromoter (OLIG1-D; a combination of four regulatory sequences from the human oligodendrocyte transcription factor 1 (OLIG1) gene) upstream of a minimal F5 mutant-frt site, an enhanced green fluorescent protein (with mutated TAA->TTA stop), a nuclear localization signal, a second minimal frt site, an SV40 early polyA signal, and a human HPRT complementary sequence (containing exon1, intron1, exon2, and part of intron2). This construct was targeted as a single copy knockin to the Hprt1b-m3 mutant locus on the X chromosome via electroporation into mEMS1204 embryonic stem cells (generated from F1 generation male pups born of C57BL/6-congenic females homozygous for a Hprt1b-m3 mutation [originally derived from 129P2/OlaHsd-derived E14TG2a embryonic stem cells] X 129S-Gt(ROSA)26Sortm1Sor heterozygous males (see Stock No. 002171 and 003310, respectively)). Correctly targeted embryonic stem cells were microinjected into recipient mice cells. The resulting chimeric males (founder line mEMS1615) were bred to B6(Cg)-Tyrc-2J/J females (B6-albino; Stock No. 000058). Female progeny (obligate Hprt1Ple151-EGFP;mEMS1615 heterozygotes) also harboring a Tyr+ allele in combination with the Aw (agouti, white belly) and a (non-agouti/black) coat color alleles were identified and bred with C57BL/6J inbred males (Stock No. 000664). Next, hemizygous Hprt1Ple151-EGFP;mEMS1615 mice were bred with C57BL/6J inbred mice for at least three generations prior to arrival at The Jackson Laboratory. Upon arrival, these mice were bred with C57BL/6J inbred mice for at least one generation to establish the live colony.
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
Fluorescent Protein Strains
View Fluorescent Protein Strains (225 strains)
Pleiades Promoter Project GFP strains
View Pleiades Promoter Project GFP strains (16 strains)
Strains carrying other alleles of GFP
View Strains carrying other alleles of GFP (117 strains)
Strains carrying other alleles of Hprt1
004302 129S1-Hprt1tm1(cre)Mnn/J 002027 129S8/SvEv-Gpi1c Hprt1b-m2/J 002171 B6.129P2-Hprt1b-m3/J 008710 B6.129P2-Hprt1tm10(Ple162-EGFP/cre)Ems/J 008877 B6.129P2-Hprt1tm12(Ple177-EGFP/cre)Ems/J 008706 B6.129P2-Hprt1tm4(Ple88-EGFP)Ems/J 008707 B6.129P2-Hprt1tm7(Ple185-EGFP)Ems/J 008709 B6.129P2-Hprt1tm9(Ple178-EGFP/cre)Ems/J 008876 B6;129-Hprt1tm11(Ple176-EGFP/cre)Ems/J 003138 B6;129-Hprt1tm1Detl/J 000807 RBJ/DnJ View Strains carrying other alleles of Hprt1 (11 strains)
Fluorescent Proteins/lacZ Systems
JAX® NOTES, Spring 2009; 513. Pleiades Promoter Project mice shine at The Jackson Laboratory.
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
GFP relatedNeurobiology Research
Fluorescent protein expression in neural tissue
Research Tools
Fluorescent Proteins
Genetics Research
Tissue/Cell Markers: glial cells
Tissue/Cell Markers: glial cells, oligodendrocytes, Schwann cells
Tissue/Cell Markers: neurons
Neurobiology Research
cell marker
Research Tools
Fluorescent Proteins
| Allele Symbol | Hprt1tm8(Ple151-EGFP)Ems | ||
|---|---|---|---|
| Allele Name | targeted mutation 8, Elizabeth M Simpson | ||
| Allele Type | Targeted (knock-in) | ||
| Common Name(s) | Hprt1tm8(OLIG1-EGFP)Ems; Hprt1tm8(Ple151-EGFP;mEMS1615)Ems; Hprt1tm8(mEMS1615)Ems; Ple151;OLIG1-D;mEMS1615; | ||
| Mutation Made By | Elizabeth Simpson, University of British Columbia | ||
| Strain of Origin | (B6.129P2-Hprt1 | ||
| ES Cell Line Name | mEMS1204 | ||
| ES Cell Line Strain | (B6.129P2-Hprt1 | ||
| Expressed Gene | GFP, Green Fluorescent Protein, jellyfish | ||
| Green Fluorescent Protein (GFP), derived from the jellyfish Aequorea victoria, is a versatile reporter molecule which has found use in many biological applications. In some constructs the original molecule has been modified in order to enhance its fluorescence intensity (EGFP, enhanced GFP). When utilized in a transgenic construct, tissue expressing sufficient amounts of GFP will fluoresce when exposed to a 488 nm light source. | |||
| Promoter | OLIG1, oligodendrocyte transcription factor 1, human | ||
| Molecular Note |
The Ple151-EGFP transgene (pEMS1172) was designed with a Ple151 minipromoter (OLIG1-D; a combination of four regulatory sequences from the human oligodendrocyte transcription factor 1 (OLIG1) gene) upstream of a minimal F5 mutant-frt site, an enhanced green fluorescent protein (with mutated TAA->TTA stop), a nuclear localization signal, a second minimal frt site, an SV40 early polyA signal, and a human HPRT complementary sequence (containing exon1, intron1, exon2, and part of intron2). This construct wastargeted as a single copy knockin to the Hprt1b-m3 mutant locus on the X chromosome. The promoter/regulatory regions of the human oligodendrocyte transcription factor 1 (OLIG1) gene direct expression of enhanced green fluorescent protein (EGFP) to neural white matter glia and oligodendroglia. EGFP expression (via anti-GFP immunocytochemistry) is observed throughout cortical and subcortical regions of the brain. Within the cortex, individual cell bodies are distinctly labeled and "puffy" processes surround these cells. In contrast to the predicted expression of OLIG1, EGFP expression does not appear to be enriched in white matter tracts or in the corpus callosum. [MGI Ref ID J:144244] | ||
| Gene Symbol and Name | Hprt1, hypoxanthine guanine phosphoribosyl transferase 1 | ||
| Chromosome | X | ||
| Gene Common Name(s) | C81579; HGPRT; HPGRT; HPRT; Hgprtase; MGC112554; expressed sequence C81579; | ||
Genotyping Protocols
Gt(ROSA)26Sortm1sor STD, Standard PCR
Helpful Links
Genotyping resources and troubleshooting
Yang GS; Banks KG; Bonaguro RJ; Wilson G; Dreolini L; de Leeuw CN; Liu L; Swanson DJ; Goldowitz D; Holt RA; Simpson EM. 2008. Next generation tools for high-throughput promoter and expression analysis employing single-copy knock-ins at the Hprt1 locus. Genomics :. [PubMed: 18950699] [MGI Ref ID J:144244]
Hprt1tm8(Ple151-EGFP)Ems relatedThe Pleiades Promoter Project, URL: http://pleiades.org/index.php. 2009. Generation of reporter and cre-expressing targeted transgenic mice in the Hprt1 gene using human MiniPromoters that drive region- and cell-specific gene expression in the mouse brain MGI Direct Data Submission :. [MGI Ref ID J:145689]
Colony Maintenance
Breeding & Husbandry The donating investigator recommends maintaining this strain by breeding heterozygous females with C57BL/6J inbred males (Stock No. 000664). Mating System Heterozygote x Inbred (Female x Male) 18-JUL-09 Diet Information LabDiet® 5K52/5K67
This strain is currently Under Development for Production.
To register your interest in this strain go to the Strain Interest Form.
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| Standard Supply | Under Development for Distribution Colony |
|---|---|
| Supply Notes |
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| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
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