Literature DB >> 2196180

Expression of spasmolysin (FIM-A.1): an integumentary mucin from Xenopus laevis.

F Hauser1, E M Gertzen, W Hoffmann.   

Abstract

In the past, a unique type of precursor for a secretory protein was discovered. It contains a central repetitive domain rich in threonine residues and terminal cysteine-rich domains. Due to striking homologies of these terminal domains with pancreatic spasmolytic polypeptide, originally the name "prepro-spasmolysin" was proposed. Here we show that the mature protein has a MW of about 130 kDa, consisting of about 70% carbohydrate and 30% protein. Similar O-linked glycoproteins have been found in mucins from human intestine. For this and numerous other reasons we decided to rename this glycoprotein "frog integumentary mucin A.1" (FIM-A.1). Furthermore, analysis of the protein with specific antibodies against the predicted C-terminal end indicates that FIM-A.1 is probably not processed at pairs of basic residues. In situ hybridization as well as immunofluorescence studies revealed that FIM-A.1 is expressed and stored exclusively in mature mucous glands of Xenopus laevis skin. Only cone cells at the proximal part of these glands do not synthesize FIM-A.1. In contrast, all other physiologically active peptides from X. laevis skin investigated so far are synthesized in granular glands. A hypothetical function of FIMs for defense against microbial infections is discussed.

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Year:  1990        PMID: 2196180     DOI: 10.1016/0014-4827(90)90230-8

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  8 in total

Review 1.  Growth factors in the gastrointestinal tract.

Authors:  N R Lemoine; H Y Leung; W J Gullick
Journal:  Gut       Date:  1992-10       Impact factor: 23.059

2.  Size polymorphisms due to changes in the number of O-glycosylated tandem repeats in the Dictyostelium discoideum glycoprotein PsA.

Authors:  A A Gooley; R Marshchalek; K L Williams
Journal:  Genetics       Date:  1992-04       Impact factor: 4.562

3.  Identification and characterization of rat intestinal trefoil factor: tissue- and cell-specific member of the trefoil protein family.

Authors:  S Suemori; K Lynch-Devaney; D K Podolsky
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-15       Impact factor: 11.205

4.  hP1.B, a human P-domain peptide homologous with rat intestinal trefoil factor, is expressed also in the ulcer-associated cell lineage and the uterus.

Authors:  F Hauser; R Poulsom; R Chinery; L A Rogers; A M Hanby; N A Wright; W Hoffmann
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

5.  Molecular aspects of restitution: functions of trefoil peptides.

Authors:  R Poulsom; D E Begos; I M Modlin
Journal:  Yale J Biol Med       Date:  1996 Mar-Apr

6.  Trefoil peptides promote epithelial migration through a transforming growth factor beta-independent pathway.

Authors:  A Dignass; K Lynch-Devaney; H Kindon; L Thim; D K Podolsky
Journal:  J Clin Invest       Date:  1994-07       Impact factor: 14.808

Review 7.  Trefoil Factor Family (TFF) Peptides and Their Diverse Molecular Functions in Mucus Barrier Protection and More: Changing the Paradigm.

Authors:  Werner Hoffmann
Journal:  Int J Mol Sci       Date:  2020-06-25       Impact factor: 5.923

8.  Trefoil Factor Family (TFF) Modules Are Characteristic Constituents of Separate Mucin Complexes in the Xenopus laevis Integumentary Mucus: In Vitro Binding Studies with FIM-A.1.

Authors:  René Stürmer; Jana Reising; Werner Hoffmann
Journal:  Int J Mol Sci       Date:  2020-03-31       Impact factor: 5.923

  8 in total

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