Cingulin, a new peripheral component of tight junctions

The tight junction (zonula occludens), a belt-like region of contact between cells of polarized epithelia, serves as a selective barrier to small molecules and as a total barrier to large molecules1,2, and is involved in the separation between lumenal and basolateral compartments of the epithelium3,4. In the electron microscope, tight junctions show focal regions of apparent fusion between the adjoining cell membranes, and freeze-fractured membranes display an elaborate network of branching and anastomosing strands1,5–8. Very little is known about the molecular composition and architecture of tight junctions. The first specific zonula occludens-associated protein, designated ZO-1, has recently been identified in mammalian epithelial and endothelial cells9. Here we describe the identification and purification of a new component of this junc-tional complex in avian brush-border cells, which we name cingulin. Cingulin is an acidic, heat-stable protein, with a highly elongated shape. Immunofluorescence and immunoelectron microscopy of brush-border cells with anti-cingulin antibodies show that cingulin is localized in the apical zone of the terminal web, at the endofacial surfaces of the zonula occludens.

[1]  J. Feramisco,et al.  Characterization of antibodies to smooth muscle myosin kinase and their use in localizing myosin kinase in nonmuscle cells. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[2]  K. Weber,et al.  The spectrin-related molecule, TW-260/240, cross-links the actin bundles of the microvillus rootlets in the brush borders of intestinal epithelial cells , 1983, The Journal of cell biology.

[3]  M. Stewart,et al.  Length of myosin rod and its proteolytic fragments determined by electron microscopy , 1984, FEBS letters.

[4]  T. Reese,et al.  Evidence for the lipidic nature of tight junction strands , 1982, Nature.

[5]  Daniel A. Goodenough,et al.  A FINE STRUCTURAL ANALYSIS OF INTERCELLULAR JUNCTIONS IN THE MOUSE LIVER , 1970, The Journal of cell biology.

[6]  D. Burgess,et al.  Structure and function of the brush-border cytoskeleton. , 1982, Cold Spring Harbor symposia on quantitative biology.

[7]  J. Siliciano,et al.  Identification of ZO-1: a high molecular weight polypeptide associated with the tight junction (zonula occludens) in a variety of epithelia , 1986, The Journal of cell biology.

[8]  M. Mooseker Organization, chemistry, and assembly of the cytoskeletal apparatus of the intestinal brush border. , 1985, Annual review of cell biology.

[9]  W. N. Burnette,et al.  "Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A. , 1981, Analytical biochemistry.

[10]  S. Lowey,et al.  Substructure of the myosin molecule. I. Subfragments of myosin by enzymic degradation. , 1969, Journal of molecular biology.

[11]  B. Kachar,et al.  On tight-junction structure , 1982, Cell.

[12]  G. Meer,et al.  The function of tight junctions in maintaining differences in lipid composition between the apical and the basolateral cell surface domains of MDCK cells. , 1986, The EMBO journal.

[13]  L. Staehelin,et al.  Structure and function of intercellular junctions. , 1974, International review of cytology.

[14]  B. Geiger,et al.  A-CAM: a 135-kD receptor of intercellular adherens junctions. I. Immunoelectron microscopic localization and biochemical studies , 1986, The Journal of cell biology.

[15]  S. Fuller,et al.  Cell surface polarity in epithelia. , 1985, Annual review of cell biology.

[16]  K. Weber,et al.  F-actin-binding and cross-linking properties of porcine brain fodrin, a spectrin-related molecule. , 1982, The Journal of biological chemistry.

[17]  B. Geiger,et al.  Immunoelectron microscope studies of membrane-microfilament interactions: distributions of alpha-actinin, tropomyosin, and vinculin in intestinal epithelial brush border and chicken gizzard smooth muscle cells , 1981, The Journal of cell biology.

[18]  K. Weber,et al.  Mapping the fodrin molecule with monoclonal antibodies. A general approach for rod-like multidomain proteins. , 1983, Journal of molecular biology.

[19]  A. Bretscher Smooth muscle caldesmon. Rapid purification and F-actin cross-linking properties. , 1984, The Journal of biological chemistry.

[20]  D. Parry,et al.  α-Helical coiled coils — a widespread motif in proteins , 1986 .

[21]  N. Hirokawa,et al.  Location of a protein of the fodrin-spectrin-TW260/240 family in the mouse intestinal brush border , 1983, Cell.

[22]  B. Jockusch,et al.  Vinculin and α-Actinin: Interaction with Actin and Effect on Microfilament Network Formation , 1982 .

[23]  L. Staehelin,et al.  The terminal web. A reevaluation of its structure and function , 1979, The Journal of cell biology.

[24]  D. Caspar,et al.  Tropomyosin: crystal structure, polymorphism and molecular interactions. , 1969, Journal of molecular biology.

[25]  S. Ebashi,et al.  Alpha-actinin, a new structural protein from striated muscle. I. Preparation and action on actomyosinàtp interaction. , 1965, Journal of biochemistry.

[26]  A. Bretscher,et al.  Fimbrin, a new microfilament-associated protein present in microvilli and other cell surface structures , 1980, The Journal of cell biology.

[27]  International cell biology 1980–1981 , 1982 .

[28]  S. Citi,et al.  Regulation in vitro of brush border myosin by light chain phosphorylation. , 1986, Journal of molecular biology.

[29]  D. Burgess,et al.  SDS microslab linear gradient polyacrylamide gel electrophoresis. , 1978, Analytical biochemistry.

[30]  S. Citi,et al.  Studies on the structure and conformation of brush border myosin using monoclonal antibodies. , 1987, European journal of biochemistry.

[31]  G. Palade,et al.  JUNCTIONAL COMPLEXES IN VARIOUS EPITHELIA , 1963, The Journal of cell biology.