IRSp53: crossing the road of membrane and actin dynamics in the formation of membrane protrusions

被引:198
作者
Scita, Giorgio [1 ,2 ]
Confalonieri, Stefano [1 ]
Lappalainen, Pekka [3 ]
Suetsugu, Shiro [4 ]
机构
[1] IFOM FIRC Inst Mol Oncol Fdn, I-20139 Milan, Italy
[2] Univ Milan, Sch Med, I-20122 Milan, Italy
[3] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[4] Univ Tokyo, Lab Membrane & Cytoskeleton Dynam, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
关键词
D O I
10.1016/j.tcb.2007.12.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A tight spatiotemporal coordination of the machineries controlling membrane bending and trafficking, and actin dynamics is crucial for the generation of cellular protrusions. Proteins that are simultaneously capable of regulating actin dynamics and sensing or inducing membrane curvature are predicted to have a prominent role. A prototypical example of this type of proteins is the insulin receptor tyrosine kinase substrate of 53 kDa, the founding member of a recently discovered family of proteins, including missing-in-metastasis and ABBA (actin-bundling protein with BAIAP2 homology). Structural, biochemical and cell biological experiments support the unique role of this family as transducers of signalling, linking the protruding membrane to the underlying actin cytoskeleton.
引用
收藏
页码:52 / 60
页数:9
相关论文
共 77 条
[41]   Structural basis of filopodia formation induced by the IRSp53/MIM homology domain of human IRSp53 [J].
Millard, TH ;
Bompard, G ;
Heung, MY ;
Dafforn, TR ;
Scott, DJ ;
Machesky, LM ;
Fütterer, K .
EMBO JOURNAL, 2005, 24 (02) :240-250
[42]   Characterisation of IRTKS, a novel IRSp53/MIM family actin regulator with distinct filament bundling properties [J].
Millard, Thomas H. ;
Dawson, John ;
Machesky, Laura M. .
JOURNAL OF CELL SCIENCE, 2007, 120 (09) :1663-1672
[43]   Control of receptor internalization, signaling level, and precise arrival at the target in guided cell migration [J].
Minina, Sofia ;
Reichman-Fried, Michal ;
Raz, Erez .
CURRENT BIOLOGY, 2007, 17 (13) :1164-1172
[44]   Genomic structure and alternative splicing of the insulin receptor tyrosine kinase substrate of 53-kDa protein [J].
Miyahara, A ;
Okamura-Oho, Y ;
Miyashita, T ;
Hoshika, A ;
Yamada, M .
JOURNAL OF HUMAN GENETICS, 2003, 48 (08) :410-414
[45]   IRSp53 is colocalised with WAVE2 at the tips of protruding lamellipodia and filopodia independently of Mena [J].
Nakagawa, H ;
Miki, H ;
Nozumi, M ;
Takenawa, T ;
Miyamoto, S ;
Wehland, J ;
Small, JV .
JOURNAL OF CELL SCIENCE, 2003, 116 (12) :2577-2583
[46]  
Nourry Claire, 2003, Sci STKE, V2003, pRE7
[47]   Identification of BAIAP2 (BAI-associated protein 2), a novel human homologue of hamster IRSp53, whose SH3 domain interacts with the cytoplasmic domain of BAI1 [J].
Oda, K ;
Shiratsuchi, T ;
Nishimori, H ;
Inazawa, J ;
Yoshikawa, H ;
Taketani, Y ;
Nakamura, Y ;
Tokino, T .
CYTOGENETICS AND CELL GENETICS, 1999, 84 (1-2) :75-82
[48]  
Okabe Shigeo, 2001, Acta Anatomica Nipponica, V76, P185
[49]  
Okamumoho Y, 1999, Nihon Rinsho, V57, P856
[50]   Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate [J].
Okamura-Oho, Y ;
Miyashita, T ;
Ohmi, K ;
Yamada, M .
HUMAN MOLECULAR GENETICS, 1999, 8 (06) :947-957