Prss8tm1.1Bug
Targeted Allele Detail
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Symbol: |
Prss8tm1.1Bug |
Name: |
serine protease 8 (prostasin); targeted mutation 1.1, Thomas H Bugge |
MGI ID: |
MGI:5588579 |
Synonyms: |
Prss8Cat- |
Gene: |
Prss8 Location: Chr7:127524889-127529266 bp, - strand Genetic Position: Chr7, 69.84 cM
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Alliance: |
Prss8tm1.1Bug page
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Germline Transmission: |
Earliest citation of germline transmission:
J:214122
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Parent Cell Line: |
W4 (ES Cell)
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Strain of Origin: |
129S6/SvEvTac
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Allele Type: |
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Targeted (Not Specified) |
Mutations: |
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Insertion, Single point mutation
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Mutation details: A T to G nucleotide substitution was introduced into exon 6 at nucleotide 943 by homologous recombination. This point mutation causes the substitution of the active site serine 238 within the catalytic histidine-aspartate-serine triad with alanine (S238A) and renders it catalytically inactive. In addition, a loxP flanked neomycin cassette under the control of the 3-phosphoglycerate kinase promoter was inserted upstream of the substitution. The neomycin cassette was removed via Cre-mediated recombination by mating with Tg(EIIa-cre)C5379Lmgd transgenic mice. RT-PCR indicates that the introduction of the point mutation and the loxP site in intron 5 do not affect mRNA expression. Western blot analysis shows that protein is expressed at levels similar to wild-type and the presence of a faster migrating species in the kidney and lung.
(J:214122)
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View phenotypes and curated references for all genotypes (concatenated display).
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Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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Carrying any Prss8 Mutation: |
24 strains or lines available
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Original: |
J:214122 Peters DE, et al., The membrane-anchored serine protease prostasin (CAP1/PRSS8) supports epidermal development and postnatal homeostasis independent of its enzymatic activity. J Biol Chem. 2014 May 23;289(21):14740-9 |
All: |
3 reference(s) |
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