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Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice
journal contribution
posted on 2023-02-07, 04:41 authored by Julian MercerJulian Mercer, A Grimes, L Ambrosini, P Lockhart, JA Paynter, H Dierick, TW GloverThe murine homologue of the Menkes disease gene (MNK) was isolated from cDNA libraries, using human cDNA clones as probes, and by PCR. The predicted amino acid sequence shows a high level of identity (89.9%) with the human protein, and the predicted functional domains in the human protein are present. Using probes to the mouse Mnk gene, we found that the mottled dappled mutation was caused by alteration in the Mnk locus and lack of expression of Mnk RNA. Tissues of the blotchy mouse contained two larger sizes of MNK mRNA demonstrating a likely defect in RNA splicing. Thus, the mottled locus is homologous to the human MNK locus and dappled and blotchy are allelic mutations in this gene. © 1994 Nature Publishing Group.
History
Journal
Nature GeneticsVolume
6Pagination
374-378Location
United StatesPublisher DOI
ISSN
1061-4036eISSN
1546-1718Language
EnglishIssue
4Publisher
NATURE PUBLISHING COUsage metrics
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Categories
Keywords
Science & TechnologyLife Sciences & BiomedicineGenetics & HeredityCOPPERMOUSECHROMOSOMEMUTANTSAdenosine TriphosphatasesAllelesAmino Acid SequenceAnimalsBase SequenceBlotting, SouthernCarrier ProteinsCation Transport ProteinsCopper-Transporting ATPasesDisease Models, AnimalFemaleFetal DiseasesGene Expression RegulationHair ColorHumansMaleMenkes Kinky Hair SyndromeMiceMice, Mutant StrainsMolecular Sequence DataProtein Structure, TertiaryRNA, MessengerRecombinant Fusion ProteinsSequence Homology, Amino AcidCopper-transporting ATPasesRare DiseasesBiotechnologyGenetics2.1 Biological and endogenous factors2 AetiologyBiological SciencesMedical and Health Sciences