FVB-Tg(Mpz*L106I)1Msch/Cnrm

Status

Available to order

EMMA IDEM:00313
International strain nameFVB-Tg(Mpz*L106I)1Msch/Cnrm
Alternative nameP0sub1
Strain typeTransgenic Strains
Allele/Transgene symbolTg(Mpz*L106I)1Msch,
Gene/Transgene symbolTg(Mpz*L106I)1Msch

Information from provider

ProviderMelitta Schachner
Provider affiliationCenter for molecular neurobiology Hamburg, Center for molecular neurobiology Hamburg
Genetic informationTo generate a mouse mutant expressing the pathogenic substitution Mpz (P0) I106L (P0sub, Gabreels-Festen et al., 1996, Fig. 1a) under the control of the Mpz promoter (Feltri et al., 1999), the 2.6BsrGI-sense vector, containing a 2.6kb-BsrGI fragment with exons 2 to 5 of the mouse Mpz genomic DNA, was used for mutagenesis. In brief, the whole vector was amplified with primers flanking and containing the mutation and was religated. A StuI/Eco47II-fragment encoding exon 2 and mutated exon 3 of the resulting 2.6BsrGI-sense P0sub vector was cloned into the mP05.7blue vector (Lemke et al., 1988, Feltri et al., 1999), containing exons 2 to 6. Finally, an EcoRI-fragment of the vector mP0Ewtblue (You et al., 1991, Feltri et al., 1999), comprising the Mpz promoter and exon 1, was inserted into the EcoRI digested mP05.7.
Phenotypic informationDistal muscle weakness and atrophy, reduced nerve conduction velocities and hypo- and dysmyelination (aberrantly folded myelin sheaths, tomacula) with "onion bulb" formation. Model of type 1b Charcot-Marie-Tooth disease.
Breeding historyThe strain was always bred on a FVB background.
References
  • Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder.;Rünker Annette E, Kobsar Igor, Fink Torsten, Loers Gabriele, Tilling Thomas, Putthoff Peggy, Wessig Carsten, Martini Rudolf, Schachner Melitta, ;2004;The Journal of cell biology;165;565-73; 15148307

Information from EMMA

Archiving centreCNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy

Literature references

  • Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder.;Rünker Annette E, Kobsar Igor, Fink Torsten, Loers Gabriele, Tilling Thomas, Putthoff Peggy, Wessig Carsten, Martini Rudolf, Schachner Melitta, ;2004;The Journal of cell biology;165;565-73; 15148307

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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*

Due to the dynamic nature of our processes strain availability may change at short notice. The local repository manager will advise you in these circumstances.

* In addition users have to cover all the shipping costs (including the cost for returning dry-shippers, where applicable).

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Practical information

Example health report
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Material Transfer Agreement (MTA)
For this strain no provider MTA is needed. Distribution is based on the EMMA conditions only.

EMMA conditions
Legally binding conditions for the transfer

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