Architecture and function of IFT complex proteins in ciliogenesis

被引:145
作者
Taschner, Michael [1 ]
Bhogaraju, Sagar [1 ]
Lorentzen, Esben [1 ]
机构
[1] Max Planck Inst Biochem, Dept Struct Cell Biol, D-82152 Martinsried, Germany
基金
奥地利科学基金会;
关键词
Cilium; Intraflagellar Transport; IFT complex; Protein domain; Protein-protein interaction; INTRAFLAGELLAR TRANSPORT PROTEIN; POLYCYSTIC KIDNEY-DISEASE; LIGHT INTERMEDIATE CHAIN; WD-REPEAT PROTEIN; ASPHYXIATING THORACIC DYSTROPHY; RIB POLYDACTYLY SYNDROMES; BARDET-BIEDL-SYNDROME; CAENORHABDITIS-ELEGANS; SENSORY CILIA; C-ELEGANS;
D O I
10.1016/j.diff.2011.11.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cilia and flagella (interchangeable terms) are evolutionarily conserved organelles found on many different types of eukaryotic cells where they fulfill important functions in motility, sensory reception and signaling. The process of Intraflagellar Transport (IFT) is of central importance for both the assembly and maintenance of cilia, as it delivers building blocks from their site of synthesis in the cell body to the ciliary assembly site at the tip of the cilium. A key player in this process is the multi-subunit IFT-complex, which acts as an adapter between the motor proteins required for movement and the ciliary cargo proteins. Since the discovery of IFT more than 15 years ago, considerable effort has gone into the purification and characterization of the IFT complex proteins. Even though this has led to very interesting findings and has greatly improved our knowledge of the IFT process, we still know very little about the overall architecture of the IFT complex and the specific functions of the various subunits. In this review we will give an update on the knowledge of the structure and function of individual IFT proteins, and the way these proteins interact to form the complex that facilitates IFT. (C) 2011 International Society of Differentiation. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:S12 / S22
页数:11
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