Ponsin/SH3P12: An 1-afadin- and vinculin-binding protein localized at cell-cell and cell-matrix adherens junctions

被引:208
作者
Mandai, K
Nakanishi, H
Satoh, A
Takahashi, K
Satoh, K
Nishioka, H
Mizoguchi, A
Takai, Y [1 ]
机构
[1] Osaka Univ, Sch Med, Dept Mol Biol & Biochem, Suita, Osaka 5650871, Japan
[2] JCR Pharmaceut Co Ltd, Japan Sci & Technol Corp, ERATO, Takai Biotimer Project,Nishi Ku, Kobe, Hyogo 6512241, Japan
[3] Kyoto Univ, Fac Med, Dept Anat & Neurobiol, Kyoto 6068501, Japan
关键词
ponsin; 1-afadin; vinculin; zonula adherens; cell-matrix adherens junction;
D O I
10.1083/jcb.144.5.1001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We recently isolated a novel actin filament (F-actin)-binding protein, afadin, that has two isoforms, 1- and s-afadins. 1-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. 1-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 1-afadin at ZA in epithelial cells and at cell-cell AJ in nonepithelial cells, we attempted here to identify an 1-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 1-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 eel-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. 1-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 1-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.
引用
收藏
页码:1001 / 1017
页数:17
相关论文
共 61 条
[1]  
ABERLE H, 1994, J CELL SCI, V107, P3655
[2]   Interspecies diversity of the occludin sequence: cDNA cloning of human, mouse, dog, and rat-kangaroo homologues [J].
AndoAkatsuka, Y ;
Saitou, M ;
Hirase, T ;
Kishi, M ;
Sakakibara, A ;
Itoh, M ;
Yonemura, S ;
Furuse, M ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1996, 133 (01) :43-47
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   The focal-adhesion vasodilator-stimulated phosphoprotein (VASP) binds to the proline-rich domain in vinculin [J].
Brindle, NPJ ;
Holt, MR ;
Davies, JE ;
Price, CJ ;
Critchley, DR .
BIOCHEMICAL JOURNAL, 1996, 318 :753-757
[5]   AN INTERACTION BETWEEN VINCULIN AND TALIN [J].
BURRIDGE, K ;
MANGEAT, P .
NATURE, 1984, 308 (5961) :744-746
[6]   Requirement for the PDZ domain protein, INAD, for localization of the TRP store-operated channel to a signaling complex [J].
Chevesich, J ;
Kreuz, AJ ;
Montell, C .
NEURON, 1997, 18 (01) :95-105
[7]  
CIMINO G, 1991, CANCER RES, V51, P6712
[8]   MODULAR BINDING DOMAINS IN SIGNAL-TRANSDUCTION PROTEINS [J].
COHEN, GB ;
REN, RB ;
BALTIMORE, D .
CELL, 1995, 80 (02) :237-248
[9]   OCCLUDIN - A NOVEL INTEGRAL MEMBRANE-PROTEIN LOCALIZING AT TIGHT JUNCTIONS [J].
FURUSE, M ;
HIRASE, T ;
ITOH, M ;
NAGAFUCHI, A ;
YONEMURA, S ;
TSUKITA, S ;
TSUKITA, S .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1777-1788
[10]   Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin [J].
Furuse, M ;
Fujita, K ;
Hiiragi, T ;
Fujimoto, K ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1998, 141 (07) :1539-1550