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本文引用的文献

1
Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.WDR19 基因突变导致的伴有骨骼异常和肾功能不全的纤毛病
Am J Hum Genet. 2011 Nov 11;89(5):634-43. doi: 10.1016/j.ajhg.2011.10.001. Epub 2011 Oct 20.
2
Mutations in Traf3ip1 reveal defects in ciliogenesis, embryonic development, and altered cell size regulation.Traf3ip1 突变导致纤毛发生缺陷、胚胎发育异常和细胞大小调节改变。
Dev Biol. 2011 Dec 1;360(1):66-76. doi: 10.1016/j.ydbio.2011.09.001. Epub 2011 Sep 16.
3
Intraflagellar transport delivers tubulin isotypes to sensory cilium middle and distal segments.鞭毛内运输将微管蛋白同工型运送到感觉纤毛的中段和远段。
Nat Cell Biol. 2011 Jun 5;13(7):790-8. doi: 10.1038/ncb2268.
4
Biochemical mapping of interactions within the intraflagellar transport (IFT) B core complex: IFT52 binds directly to four other IFT-B subunits.鞭毛内运输(IFT)B 核心复合物内部相互作用的生化图谱:IFT52 直接与其他四个 IFT-B 亚基结合。
J Biol Chem. 2011 Jul 29;286(30):26344-52. doi: 10.1074/jbc.M111.254920. Epub 2011 Jun 3.
5
Crystal structure of the intraflagellar transport complex 25/27.鞭毛内运输复合物 25/27 的晶体结构。
EMBO J. 2011 May 18;30(10):1907-18. doi: 10.1038/emboj.2011.110. Epub 2011 Apr 19.
6
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.人类和小鼠 WDR35 突变导致短肋多指畸形综合征,原因是纤毛发生异常。
Am J Hum Genet. 2011 Apr 8;88(4):508-15. doi: 10.1016/j.ajhg.2011.03.015.
7
The cilia protein IFT88 is required for spindle orientation in mitosis.纤毛蛋白 IFT88 是有丝分裂中纺锤体定向所必需的。
Nat Cell Biol. 2011 Apr;13(4):461-8. doi: 10.1038/ncb2202. Epub 2011 Mar 27.
8
Ciliogenesis: building the cell's antenna.纤毛发生:构建细胞的天线。
Nat Rev Mol Cell Biol. 2011 Apr;12(4):222-34. doi: 10.1038/nrm3085.
9
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome.C14ORF179 编码的 IFT43 突变与 Sensenbrenner 综合征相关。
J Med Genet. 2011 Jun;48(6):390-5. doi: 10.1136/jmg.2011.088864. Epub 2011 Mar 4.
10
IFT20 is required for opsin trafficking and photoreceptor outer segment development.IFT20 对于视蛋白运输和光感受器外节发育是必需的。
Mol Biol Cell. 2011 Apr;22(7):921-30. doi: 10.1091/mbc.E10-09-0792. Epub 2011 Feb 9.

纤毛发生中IFT 复合物蛋白的结构与功能。

Architecture and function of IFT complex proteins in ciliogenesis.

机构信息

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, Am Klopferspitz 18, D-82152 Martinsried, Germany.

出版信息

Differentiation. 2012 Feb;83(2):S12-22. doi: 10.1016/j.diff.2011.11.001. Epub 2011 Nov 25.

DOI:10.1016/j.diff.2011.11.001
PMID:22118932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3977345/
Abstract

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.

摘要

纤毛和鞭毛(可互换使用)是在许多不同类型的真核细胞中发现的进化上保守的细胞器,它们在运动、感觉接收和信号转导中发挥着重要作用。内鞭毛运输(IFT)过程对于纤毛的组装和维持至关重要,因为它将构建块从细胞体中的合成部位运送到纤毛组装部位的尖端。在这个过程中,多亚基 IFT 复合物是一个关键的参与者,它作为运动所需的马达蛋白和纤毛货物蛋白之间的适配器。自 IFT 发现 15 年多以来,已经投入了相当大的努力来纯化和表征 IFT 复合物蛋白。尽管这导致了非常有趣的发现,并大大提高了我们对 IFT 过程的认识,但我们仍然对 IFT 复合物的整体结构和各个亚基的特定功能知之甚少。在这篇综述中,我们将更新关于单个 IFT 蛋白的结构和功能的知识,以及这些蛋白相互作用形成促进 IFT 的复合物的方式。