The central domain of bovine submaxillary mucin consists of over 50 tandem repeats of 329 amino acids
Open Access
- 1 April 2000
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 267 (8) , 2208-2217
- https://doi.org/10.1046/j.1432-1327.2000.01225.x
Abstract
We previously elucidated five distinct protein domains (I–V) for bovine submaxillary mucin, which is encoded by two genes, BSM1 and BSM2. Using Southern blot analysis, genomic cloning and sequencing of the BSM1 gene, we now show that the central domain (V) consists of ≈ 55 tandem repeats of 329 amino acids and that domains III–V are encoded by a 58.4-kb exon, the largest exon known for all genes to date. The BSM1 gene was mapped by fluorescence in situ hybridization to the proximal half of chromosome 5 at bands q2.2–q2.3. The amino-acid sequence of six tandem repeats (two full and four partial) were found to have only 92–94% identities. We propose that the variability in the amino-acid sequences of the mucin tandem repeat is important for generating the combinatorial library of saccharides that are necessary for the protective function of mucins. The deduced peptide sequences of the central domain match those determined from the purified bovine submaxillary mucin and also show 68–94% identity to published peptide sequences of ovine submaxillary mucin. This indicates that the core protein of ovine submaxillary mucin is closely related to that of bovine submaxillary mucin and contains similar tandem repeats in the central domain. In contrast, the central domain of porcine submaxillary mucin is reported to consist of 81-amino-acid tandem repeats. However, both bovine submaxillary mucin and porcine submaxillary mucin contain similar N-terminal and C-terminal domains and the corresponding genes are in the conserved linkage regions of the respective genomes.Keywords
This publication has 54 references indexed in Scilit:
- Sequence of a Second Gene Encoding Bovine Submaxillary Mucin: Implication for Mucin Heterogeneity and CloningBiochemical and Biophysical Research Communications, 1998
- The Amino-Terminal Sequence of MUC5B Contains Conserved Multifunctional D Domains: Implications for Tissue-Specific Mucin FunctionsBiochemical and Biophysical Research Communications, 1998
- Molecular Cloning of Human Gastric Mucin MUC5AC Reveals Conserved Cysteine-Rich D-Domains and a Putative Leucine Zipper MotifBiochemical and Biophysical Research Communications, 1998
- Human Mucin Genes Assigned to 11p15.5: Identification and Organization of a Cluster of GenesGenomics, 1996
- Structure and Chromosomal Localization of the Human Salivary Mucin Gene, MUC7Genomics, 1996
- Standardization of cattle karyotype nomenclature: Report of the committee for the standardization of the cattle karyotypeCytogenetic and Genome Research, 1996
- UDPgalactose:glycoprotein–N‐acetyl‐d‐galactosamine 3‐β‐d‐galactosyltransferase activity synthesizing O‐glycan core 1 is controlled by the amino acid sequence and glycosylation of glycopeptide substratesEuropean Journal of Biochemistry, 1994
- Regional localization of the intestinal mucin gene MUC3 to chromosome 7q22Annals of Human Genetics, 1992
- Control of mucin synthesis: the peptide portion of synthetic O-glycopeptide substrates influences the activity of O-glycan core 1 uridine 5'-diphospho-galactose:N-acetyl-.alpha.-galactosaminyl-.alpha.-R .beta.3-galactosyltransferaseBiochemistry, 1990
- THE MOLECULAR WEIGHT OF BOVINE and PORCINE SUBMAXILLARY MUCINSInternational Journal of Protein Research, 1970