MOLECULAR-BASIS FOR THE RHINO (HR(RH-8J)) PHENOTYPE - A NONSENSE MUTATION IN THE MOUSE HAIRLESS GENE

Citation
W. Ahmad et al., MOLECULAR-BASIS FOR THE RHINO (HR(RH-8J)) PHENOTYPE - A NONSENSE MUTATION IN THE MOUSE HAIRLESS GENE, Genomics (San Diego, Calif.), 53(3), 1998, pp. 383-386
Citations number
18
Categorie Soggetti
Biothechnology & Applied Migrobiology","Genetics & Heredity
ISSN journal
08887543
Volume
53
Issue
3
Year of publication
1998
Pages
383 - 386
Database
ISI
SICI code
0888-7543(1998)53:3<383:MFTR(P>2.0.ZU;2-C
Abstract
The hairless (hr) and rhino (hr(rh)) mutations are autosomal recessive allelic mutations that map to mouse Chromosome 14. Both hairless and rhino mice have a number of skin and nail abnormalities and develop a striking form of total alopecia at approximately 3-4 weeks of age. The molecular basis of the hairless mouse phenotype was previously found to be the result of a murine leukemia proviral insertion in intron 6 o f the hr gene that resulted in aberrant splicing. In this study, we re port a 2-bp substitution in exon 4 of the hr gene in a second allele o f hr, rhino 85 (hr(rh-8J)), leading to a nonsense mutation. These find ings document the molecular basis of the rhino phenotype for the first time and suggest that rhino is a functional knock-out of the hr gene. (C) 1998 Academic Press.