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Frog integumentary mucin B.1 (FIM-B.1) represents a polymorphic extracellular mosaic protein which contains tandemly arranged serine/threonine-rich modules as well as cysteine-rich domains. The latter are probably important for oligomerization of FIM-B.1 and have also been found in many proteins of the complement cascade as well as regions homologous to von Willebrand factor. The repetitive modules are targets for extensive O-glycosylation. Previous cDNA cloning experiments clearly established polydispersities within the same individual, which originate from deletions/insertions in the repetitive domain. Here, we analyse part of the corresponding genomic region. Each repetitive unit as well as the cysteine-rich domain is encoded by an individual class 1-1 exon typical of shuffled modules. Alternative splicing of these multiple cassettes creates the polydisperse FIM-B.1 transcripts.
Baltimore,
Gene conversion: some implications for immunoglobulin genes.
1981, Pubmed
Baltimore,
Gene conversion: some implications for immunoglobulin genes.
1981,
Pubmed Bork,
Shuffled domains in extracellular proteins.
1991,
Pubmed Breathnach,
Organization and expression of eucaryotic split genes coding for proteins.
1981,
Pubmed Carlstedt,
Mucous glycoproteins: a gel of a problem.
1985,
Pubmed Granovsky,
UDPgalactose:glycoprotein-N-acetyl-D-galactosamine 3-beta-D-galactosyltransferase activity synthesizing O-glycan core 1 is controlled by the amino acid sequence and glycosylation of glycopeptide substrates.
1994,
Pubmed Hauser,
P-domains as shuffled cysteine-rich modules in integumentary mucin C.1 (FIM-C.1) from Xenopus laevis. Polydispersity and genetic polymorphism.
1992,
Pubmed
,
Xenbase Hoffmann,
A new repetitive protein from Xenopus laevis skin highly homologous to pancreatic spasmolytic polypeptide.
1988,
Pubmed
,
Xenbase Hoffmann,
Biosynthesis of frog skin mucins: cysteine-rich shuffled modules, polydispersities and genetic polymorphism.
1993,
Pubmed
,
Xenbase Hoffmann,
Biosynthesis and molecular architecture of gel-forming mucins: implications from an amphibian model system.
1995,
Pubmed Jentoft,
Why are proteins O-glycosylated?
1990,
Pubmed Lamblin,
The carbohydrate diversity of human respiratory mucins: a protection of the underlying mucosa?
1991,
Pubmed Lancaster,
Structure and expression of the human polymorphic epithelial mucin gene: an expressed VNTR unit.
1990,
Pubmed Lesuffleur,
Mucins in normal and neoplastic human gastrointestinal tissues.
1994,
Pubmed López,
Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications.
1992,
Pubmed Maizel,
Enhanced graphic matrix analysis of nucleic acid and protein sequences.
1981,
Pubmed O'Connell,
The influence of flanking sequences on O-glycosylation.
1991,
Pubmed Pollex-Krüger,
Preferred conformations and dynamics of five core structures of mucin type O-glycans determined by NMR spectroscopy and force field calculations.
1993,
Pubmed Post,
Structure of the gene for human complement protein decay accelerating factor.
1990,
Pubmed Probst,
The polymorphic integumentary mucin B.1 from Xenopus laevis contains the short consensus repeat.
1992,
Pubmed
,
Xenbase Probst,
An integumentary mucin (FIM-B.1) from Xenopus laevis homologous with von Willebrand factor.
1990,
Pubmed
,
Xenbase Swallow,
The human tumour-associated epithelial mucins are coded by an expressed hypervariable gene locus PUM.
,
Pubmed Taylor-Papadimitriou,
Exploiting altered glycosylation patterns in cancer: progress and challenges in diagnosis and therapy.
1994,
Pubmed Toribara,
MUC-2 human small intestinal mucin gene structure. Repeated arrays and polymorphism.
1991,
Pubmed Vavasseur,
O-glycan biosynthesis in human colorectal adenoma cells during progression to cancer.
1994,
Pubmed Wysocki,
Gene conversion and the generation of antibody diversity.
1989,
Pubmed