B6J;129-MpdzGt(XG734)Byg/WtsiH

Status

Available to order

EMMA IDEM:15869
Citation informationRRID:IMSR_EM:15869 

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International strain nameB6J;129-MpdzGt(XG734)Byg/WtsiH
Alternative nameB6J;129-Mpdz/H
Strain typeGene-trap
Allele/Transgene symbolMpdzGt(XG734)Byg
Gene/Transgene symbolMpdz

Information from provider

ProviderSeth Grant
Provider affiliationWellcome Trust Sanger Institute
Genetic informationInformation submitted by depositor: This strain displays issues with morbidity in homozygotes. The phenotype is on heterozygotes but they can generate homozygotes in timed matings. Maintain on a C57BL/6J background. Information sourced from supplementary data for https://doi.org/10.1101/500389: This strain carries the gene-trapping vector pGT1lxf was used to insert the mutation in ES cell line XG734. The insertional mutation was designed to create an in-frame fusion between the 5' exons of the trapped gene and a reporter, a fusion of beta-galactosidase and neomycin phosphotransferase. Thus, the gene-trapped locus is predicted to yield a fusion transcript containing exons 1-11 of Mpdz and beta-galactosidase. Western blots of brain extracts from knockout homozygote pups confirmed the deletion and absence of full length encoded protein
Phenotypic informationHomozygous:
Homozygous displayed increased perinatal mortality rates from birth to 4 weeks but tissue was collected for post mortem genotyping

Heterozygous:
Heterozygous mice consumed significantly less of 6%, 10%, and 20% ethanol solutions per kilogram body weight each day compared to wildtype littermates.
Breeding historyBackcrosses onto the C57BL/6 background were used to maintain the colony and to generate heterozygous and wildtype mice to study. Genomic composition of the majority of mice used in experiments was approximately 25% 129P2/OlaHsd and 75% C57BL/6
References
  • Novel MPDZ/MUPP1 transgenic and knockdown models confirm Mpdz's role in ethanol withdrawal and support its role in voluntary ethanol consumption.;Milner Lauren C, Shirley Renee L, Kozell Laura B, Walter Nicole A, Kruse Lauren C, Komiyama Noboru H, Grant Seth G N, Buck Kari J, ;2015;Addiction biology;20;143-7; 24118405
Homozygous fertilenot known
Homozygous viableno
Homozygous matings requirednot known
Immunocompromisednot known

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom

Disease and phenotype information

IMPC phenotypes (gene matching)
  • abnormal auditory brainstem response / IMPC
  • abnormal retina morphology / IMPC
  • abnormal retina blood vessel morphology / IMPC
  • decreased grip strength / IMPC
  • abnormal retina vasculature morphology / IMPC
  • increased circulating potassium level / IMPC
  • decreased startle reflex / IMPC
  • increased heart weight / IMPC
  • improved glucose tolerance / IMPC

Literature references

  • Novel MPDZ/MUPP1 transgenic and knockdown models confirm Mpdz's role in ethanol withdrawal and support its role in voluntary ethanol consumption.;Milner Lauren C, Shirley Renee L, Kozell Laura B, Walter Nicole A, Kruse Lauren C, Komiyama Noboru H, Grant Seth G N, Buck Kari J, ;2015;Addiction biology;20;143-7; 24118405

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Availabilities

Requesting frozen sperm or embryos is generally advisable wherever possible, in order to minimise the shipment of live mice.

  • Frozen embryos. Delivered in 4 weeks (after paperwork in place). €1740*
  • Rederivation of mice from frozen stock, delivery time available upon request . €3880*
  • Tissue - Types of tissue, service fee and delivery time available upon request

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Practical information

Genotyping protocol

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