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PMID: 10085297 Published · ppublish English Journal Article

Ponsin/SH3P12: an l-afadin- and vinculin-binding protein localized at cell-cell and cell-matrix adherens junctions.

The Journal of cell biology ·Vol. 144 ·No. 5 ·1999-03-08 ·Pages 1001-17

Mandai K, Nakanishi H, Satoh A, Takahashi K, Satoh K, Nishioka H, Mizoguchi A, Takai Y

Abstract

We recently isolated a novel actin filament (F-actin)-binding protein, afadin, that has two isoforms, l- and s-afadins. l-Afadin is ubiquitously expressed and specifically localized at zonula adherens (ZA) in epithelial cells and at cell-cell adherens junction (AJ) in nonepithelial cells, whereas s-afadin is abundantly expressed in neural tissue. l-Afadin has one PDZ domain, three proline-rich regions, and one F-actin-binding domain, whereas s-afadin lacks the third proline-rich region and the F-actin-binding domain. To understand the molecular mechanism of the specific localization of l-afadin at ZA in epithelial cells and at cell-cell AJ in nonepithelial cells, we attempted here to identify an l-afadin-binding protein(s) and isolated a protein, named ponsin. Ponsin had many splicing variants and the primary structures of two of them were determined. Both the two variants had three Src homology 3 (SH3) domains and turned out to be splicing variants of SH3P12. The third proline-rich region of l-afadin bound to the region of ponsin containing the second and third SH3 domains. Ponsin was ubiquitously expressed and localized at ZA in epithelial cells, at cell-cell AJ in nonepithelial cells, and at cell-matrix AJ in both types of cells. Ponsin furthermore directly bound vinculin, an F-actin-binding protein localized at ZA in epithelial cells, at cell-cell AJ in nonepithelial cells, and at cell-matrix AJ in both types of cells. Vinculin has one proline-rich region where two proline-rich sequences are located. The proline-rich region bound to the region of ponsin containing the first and second SH3 domains. l-Afadin and vinculin bound to ponsin in a competitive manner and these three proteins hardly formed a ternary complex. These results indicate that ponsin is an l-afadin- and vinculin-binding protein localized at ZA in epithelial cells, at cell-cell AJ in nonepithelial cells, and at cell-matrix AJ in both types of cells.

MeSH Terms
Amino Acid Sequence Animals Base Sequence COS Cells Cell Membrane/metabolism DNA, Complementary Kinesins Mice Microfilament Proteins/genetics,isolation & purification,metabolism Microscopy, Fluorescence Microscopy, Immunoelectron Molecular Sequence Data Myosins Protein Binding Sequence Homology, Amino Acid Tumor Cells, Cultured Vinculin/metabolism
Chemicals
Afdn protein, mouse DNA, Complementary Microfilament Proteins afadin ponsin Vinculin Myosins Kinesins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Mandai K
Takai Biotimer Project, ERATO, Japan Science and Technology Corporation, c/o JCR Pharmaceuticals Co., Ltd., 2-2-10 Murotani, Nishi-ku, Kobe 651-2241, Japan.
Nakanishi H
Satoh A
Takahashi K
Satoh K
Nishioka H
Mizoguchi A
Takai Y
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1999-03-08
Pages
1001-17
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2148189
Subset
IM
Databases
GENBANK
AF078666, AF078667
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