Cnbc:NMRI-Tg(Tyr*)2138Lmon

Status

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EMMA IDEM:03102
Citation informationRRID:IMSR_EM:03102 

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International strain nameCnbc:NMRI-Tg(Tyr*)2138Lmon
Alternative nameYRT4
Strain typeTransgenic Strains
Allele/Transgene symbolTg(Tyr*)2138Lmon, Tyrc
Gene/Transgene symbolTg(Tyr*)2138Lmon, Tyr

Information from provider

ProviderLluis Montoliu
Provider affiliationDepartamento de Biologia Molecular y Celular, CNB-CSIC, Centro Nacional de Biotecnologia
Additional ownerProf. Dr. Günther Schütz, DKFZ, Dept. Molecular Biology of the Cell I, Heidelberg, Germany
Genetic informationTransgenic mice carrying 1 copy of the 100 kb YAC YRT4 containing the entire mouse tyrosinase gene, including all five exons, 5' UTR and 3' UTR without the LCR regulatory element. YRT4 YAC was obtained after removing 150 kb of DNA including LCR and upstream sequences, by homologous recombination of YRT2 YAC (Montoliu et al. 1996; EMBO J 15:6026-34). Mice were generated in the albino outbred WinHsd:NMRI background whose albino phenotype was partially rescued by the YAC YRT4 transgene, thereby becoming light pigmented (light grey, patchy, coat colour variegation) and eye pigmented. The YAC YRT4 is derived from a YAC library made from C3H mouse genomic DNA.
Phenotypic informationLightly pigmented, variegated, black eyes. Transgenic mice YRT4 in the NMRI background have pigmented eyes and very light skin pigmentation, variegated coat colour, with patches of pigmented skin and hair. They have partially rescued the retinal and visual abnormalities associated with albinism. In particular, they have variegation in retinal pigment epithelium cells with a peculiar distribution of pigmentation, resulting in peripheral retina being mostly pigmented and central retina being mostly albino.
Breeding historyTransgenic mice YRT4 were generated in 1994/95 by pronuclear microinjection using fertilised albino outbred NMRI oocytes and have been maintained as hemizygous since then in the same background.
References
  • A locus control region at -12 kb of the tyrosinase gene.;Montoliu L, Umland T, Schütz G, ;1996;The EMBO journal;15;6026-34; 8947025
  • Artificial chromosome transgenesis in pigmentary research.;Giraldo Patricia, Montoliu Lluís, ;2002;Pigment cell research;15;258-64; 12100491
  • Variegated expression and delayed retinal pigmentation during development in transgenic mice with a deletion in the locus control region of the tyrosinase gene.;Giménez E, Giraldo P, Jeffery G, Montoliu L, ;2001;Genesis (New York, N.Y. : 2000);30;21-5; 11353514
  • Regional abnormalities in retinal development are associated with local ocular hypopigmentation.;Giménez Estela, Lavado Alfonso, Jeffery Glen, Montoliu Lluís, ;2005;The Journal of comparative neurology;485;338-47; 15803509
  • A strategy to study tyrosinase transgenes in mouse melanocytes.;Lavado Alfonso, Matheu Ander, Serrano Manuel, Montoliu Lluís, ;2005;BMC cell biology;6;18; 15826307
  • New animal models to study the role of tyrosinase in normal retinal development.;Lavado Alfonso, Montoliu Lluis, ;2006;Frontiers in bioscience : a journal and virtual library;11;743-52; 16146766
Homozygous fertileyes
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreCNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain
Animals used for archivingheterozygous NMRI males, wild-type NMRI females
Stage of embryos8-cell

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

MGI phenotypes (allele matching)
  • absent coat pigmentation / MGI
  • diluted coat color / MGI
  • abnormal coat/hair pigmentation / MGI
  • absent eye pigmentation / MGI
  • abnormal coat appearance / MGI
  • decreased eye pigmentation / MGI
  • mottled coat / MGI
  • abnormal eye pigmentation / MGI
  • belly spot / MGI
  • hypopigmentation / MGI
  • variegated eye pigmentation pattern / MGI
  • decreased ear pigmentation / MGI
MGI phenotypes (gene matching)
  • abnormal cell morphology / MGI
  • diluted coat color / MGI
  • irregular coat pigmentation / MGI
  • belly spot / MGI
  • absent hair follicle melanin granules / MGI
  • shiny fur / MGI
  • mottled coat / MGI
  • abnormal retinal photoreceptor morphology / MGI
  • pigmentation phenotype / MGI
  • absent skin pigmentation / MGI
  • abnormal keratinocyte apoptosis / MGI
  • abnormal eye pigmentation / MGI
  • abnormal retina morphology / MGI
  • retinal degeneration / MGI
  • decreased retinal photoreceptor cell number / MGI
  • abnormal coat appearance / MGI
  • male infertility / MGI
  • abnormal coat/hair pigmentation / MGI
  • prenatal lethality / MGI
  • premature death / MGI
  • abnormal vision / MGI
  • abnormal skin pigmentation / MGI
  • no abnormal phenotype detected / MGI
  • no phenotypic analysis / MGI
  • abnormal cell nucleus morphology / MGI
  • failure of zygotic cell division / MGI
  • single kidney / MGI
  • absent seminal vesicle / MGI
  • abnormal chromosome morphology / MGI
  • chromosome breakage / MGI
  • induced chromosome breakage / MGI
  • increased cellular sensitivity to ionizing radiation / MGI
  • abnormal miscarriage rate / MGI
  • abnormal hair follicle melanogenesis / MGI
  • abnormal melanosome morphology / MGI
  • abnormal iris pigmentation / MGI
  • absent coat pigmentation / MGI
  • decreased eye pigmentation / MGI
  • abnormal aqueous drainage system morphology / MGI
  • abnormal retinal ganglion layer morphology / MGI
  • abnormal eye physiology / MGI
  • abnormal intraocular pressure / MGI
  • variegated coat color / MGI
  • homeostasis/metabolism phenotype / MGI
  • reproductive system phenotype / MGI
  • vision/eye phenotype / MGI
  • hypopigmentation / MGI
  • ocular albinism / MGI
  • absent eye pigmentation / MGI
  • decreased survivor rate / MGI
  • transverse fur striping / MGI
  • mortality/aging / MGI
  • abnormal survival / MGI
  • integument phenotype / MGI
  • neonatal lethality, complete penetrance / MGI
  • perinatal lethality, complete penetrance / MGI
  • prenatal lethality, complete penetrance / MGI
  • embryonic lethality, complete penetrance / MGI
  • embryonic lethality at implantation, complete penetrance / MGI
  • embryonic lethality before implantation, complete penetrance / MGI
  • decreased ear pigmentation / MGI
  • variegated eye pigmentation pattern / MGI
  • decreased a wave amplitude / MGI
  • decreased b wave amplitude / MGI

Literature references

  • A locus control region at -12 kb of the tyrosinase gene.;Montoliu L, Umland T, Schütz G, ;1996;The EMBO journal;15;6026-34; 8947025
  • Artificial chromosome transgenesis in pigmentary research.;Giraldo Patricia, Montoliu Lluís, ;2002;Pigment cell research;15;258-64; 12100491
  • Variegated expression and delayed retinal pigmentation during development in transgenic mice with a deletion in the locus control region of the tyrosinase gene.;Giménez E, Giraldo P, Jeffery G, Montoliu L, ;2001;Genesis (New York, N.Y. : 2000);30;21-5; 11353514
  • Regional abnormalities in retinal development are associated with local ocular hypopigmentation.;Giménez Estela, Lavado Alfonso, Jeffery Glen, Montoliu Lluís, ;2005;The Journal of comparative neurology;485;338-47; 15803509
  • A strategy to study tyrosinase transgenes in mouse melanocytes.;Lavado Alfonso, Matheu Ander, Serrano Manuel, Montoliu Lluís, ;2005;BMC cell biology;6;18; 15826307
  • New animal models to study the role of tyrosinase in normal retinal development.;Lavado Alfonso, Montoliu Lluis, ;2006;Frontiers in bioscience : a journal and virtual library;11;743-52; 16146766

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  • Frozen embryos. Delivered in 4 weeks (after paperwork in place). €1740*
  • Frozen sperm. Delivered in 4 weeks (after paperwork in place). €1740*
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