C.129P2-Krt18tm1Tmm/Ieg

Status

Available to order

EMMA IDEM:01743
Citation informationRRID:IMSR_EM:01743 

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International strain nameC.129P2-Krt18tm1Tmm/Ieg
Alternative nameK18(-/-) knock-out
Strain typeTargeted Mutant Strains : Knock-out
Allele/Transgene symbolKrt18tm1Tmm
Gene/Transgene symbolKrt18

Information from provider

ProviderThomas Magin
Provider affiliationInstitute of physiological chemistry / Dept. of cellular biochemistry, University of Bonn
Genetic informationAn Hprt minigene replaced most of exon 1, intron 1 and exon 2 of the keratin 18 (Krt18) gene via homologous recombination in ES cells.
Phenotypic informationKrt18 null mice are viable, fertile, and show a normal lifespan. In young Krt18 null mice, hepatocytes were completely devoid of keratin filaments. Old Krt18 null mice, however, developed a distinctive liver pathology with abnormal hepatocytes containing Krt8-positive aggregates. These stained positively for ubiquitin and MM120-1 Mallory antigen and were identified as Mallory bodies, one hallmark of human alcoholic hepatitis. Another striking finding was the absence or drastic down-regulation of Krt7 in several tissues despite its ongoing transcription. However, double-deficiency for Krt18 and Krt19 led to complete loss of keratin filaments in early mouse development. These embryos died at around day E9.5 with 100% penetrance (Hesse et al., 2000).
Breeding historyOffspring of the chimaeras were mated to BALB/c mice for further analysis. K18-/- mice have been backcrossed to the BALB/c background for 7 generations.
References
  • Lessons from keratin 18 knockout mice: formation of novel keratin filaments, secondary loss of keratin 7 and accumulation of liver-specific keratin 8-positive aggregates.;Magin T M, Schröder R, Leitgeb S, Wanninger F, Zatloukal K, Grund C, Melton D W, ;1998;The Journal of cell biology;140;1441-51; 9508776
  • Targeted deletion of keratins 18 and 19 leads to trophoblast fragility and early embryonic lethality.;Hesse M, Franz T, Tamai Y, Taketo M M, Magin T M, ;2000;The EMBO journal;19;5060-70; 11013209

Information from EMMA

Archiving centreHelmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany

Disease and phenotype information

MGI phenotypes (allele matching)
  • enlarged liver / MGI
MGI phenotypes (gene matching)
  • enlarged liver / MGI

Literature references

  • Lessons from keratin 18 knockout mice: formation of novel keratin filaments, secondary loss of keratin 7 and accumulation of liver-specific keratin 8-positive aggregates.;Magin T M, Schröder R, Leitgeb S, Wanninger F, Zatloukal K, Grund C, Melton D W, ;1998;The Journal of cell biology;140;1441-51; 9508776
  • Targeted deletion of keratins 18 and 19 leads to trophoblast fragility and early embryonic lethality.;Hesse M, Franz T, Tamai Y, Taketo M M, Magin T M, ;2000;The EMBO journal;19;5060-70; 11013209

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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*

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Practical information

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