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Published on: July 9, 2016
Mouse gastric mucin: cloning and chromosomal localization
L L Shekels1, C Lyftogt, M Kieliszewski
1Department of Medicine, University of Minnesota, Minneapolis 55417, USA.
The Biochemical Journal
|November 1, 1995
Summary
Researchers cloned a mouse gastric mucin (MGM), identifying a novel tandem repeat sequence. This discovery provides a foundation for studying gastric mucin gene regulation and its role in protecting the stomach lining.
Area of Science:
- Biochemistry
- Molecular Biology
- Genetics
Background:
- Mucins are crucial for protecting the gastric epithelium by maintaining pH and preventing self-digestion.
- Understanding mucin gene regulation is vital for analyzing gastric health and disease.
Purpose of the Study:
- To clone a mouse gastric mucin (MGM) gene.
- To establish a basis for investigating mucin gene regulation in the stomach.
Main Methods:
- Purification and deglycosylation of mouse gastric mucin.
- Antibody generation against native and deglycosylated MGM.
- Screening of a mouse stomach cDNA library.
- Northern blot analysis and DNA analysis.
- Gene mapping to mouse chromosome 7.
Main Results:
- Partial cDNA clones of MGM were obtained, containing a novel 16-amino acid tandem repeat (QTSSPNTGKTSTISTT) and non-repetitive sequence.
- The MGM tandem repeat showed no similarity to known mucins, but the non-repetitive region shared similarity with human MUC5AC.
- MGM mRNA was predominantly expressed in the mouse stomach (≥13.5 kb), with no expression in other tested organs.
- Immunoreactivity localized MGM to superficial mucous cells and specific glands.
- The MGM gene maps to mouse chromosome 7, homologous to the human MUCIN gene cluster.
Conclusions:
- The cloned mouse gastric mucin (MGM) represents a homologue of human MUC5AC, named Muc5ac.
- The novel tandem repeat sequence in MGM expands the known diversity of mucin structures.
- This study provides essential tools and data for future research into gastric mucin gene regulation and function.

