Journal article
A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus
Human molecular genetics, Vol.2(10), pp.1561-1569
1993
DOI: 10.1093/hmg/2.10.1561
PMID: 7505691
Abstract
To develop an animal model for cystic fibrosis (CF), targeted gene disruption in embryonic stem (ES) cells was used to generate a duplication of exon 3 (cftrm1Bay allele) of the mouse CF gene. ES cells containing this mutation were used to generate chimeric animals that transmitted the mutant allele through the germline. Homozygous mutant animals display a severe phenotype, with approximately 40% dying within 1 week from intestinal obstruction. RNAase protection analysis of the cftrm1Bay allele did not detect any normal mRNA (< 1-2% of wild-type) in mutant animals. Pathologic changes in the intestines from mutant mice included mucus accumulation in the crypts and intestinal lumen, dilatation of the bases of the crypts, enlargement of goblet cells, and the presence of concretions in the crypts or between the villi. Changes were also present in the mucosal glands of the pharynx and the minor sublingual glands, where dilatation of acini and accumulation of eosinophilic material were evident. Atrophy of acinar cells that may be secondary to nutritional deficiency and mild inflammation in the main pancreatic duct were present in the pancreas of mutant animals. No changes were noted in the lung, trachea, liver, or male reproductive tract of mutant animals, and mutant males were fertile. Homozygous mutant mice showed defects in cAMP-mediated ion transport both in ileum and in cultured fetal tracheal explants. Thus, an additional mouse model for CF has been generated that should prove useful for the understanding of the pathogenesis and the development of treatments for CF.
Details
- Title: Subtitle
- A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus
- Creators
- Wanda K O'NealPaul HastyPaul B McCrayBrett CaseyJalme RiveraPérezMichael J WelshArthur L BeaudetAllan Bradley
- Resource Type
- Journal article
- Publication Details
- Human molecular genetics, Vol.2(10), pp.1561-1569
- DOI
- 10.1093/hmg/2.10.1561
- PMID
- 7505691
- ISSN
- 0964-6906
- eISSN
- 1460-2083
- Language
- English
- Date published
- 1993
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Microbiology and Immunology; Pulmonary Medicine; Stead Family Department of Pediatrics; Neurosurgery; Internal Medicine
- Record Identifier
- 9984020849302771