When cilia go bad: cilia defects and ciliopathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Link
http://www.nature.com/articles/nrm2278.pdf
Reference130 articles.
1. Quarmby, L. M. & Parker, J. D. Cilia and the cell cycle? J. Cell Biol. 169, 707–710 (2005).
2. Fowkes, M. E. & Mitchell, D. R. The role of preassembled cytoplasmic complexes in assembly of flagellar dynein subunits. Mol. Biol. Cell 9, 2337–2347 (1998).
3. Rosenbaum, J. L. & Witman, G. B. Intraflagellar transport. Nature Rev. Mol. Cell Biol. 3, 813–825 (2002). This excellent article provides a detailed and comprehensive overview of IFT and various associated physiological aspects.
4. Avidor-Reiss, T. et al. Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis. Cell 117, 527–539 (2004). These authors used phylogenetic screening by comparative genomics to identify genes that are essential for cilia formation and function. They also discuss the difference between IFT-dependent compartmentalized ciliogenesis and cytosolic ciliogenesis, which is independent from IFT.
5. Pazour, G. J. et al. Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J. Cell Biol. 151, 709–718 (2000). This article provides evidence that IFT is essential for primary cilia assembly and function in mammals and that defects in cilia assembly can lead to polycystic kidney disease.
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