The motile cilium in development and disease: emerging new insights
- PMID: 19492356
- DOI: 10.1002/bies.200900031
The motile cilium in development and disease: emerging new insights
Abstract
In this paper, I review a collection of recently published papers that have provided significant new information about the biogenesis and functions of motile cilia. In vertebrates, the activity of motile cilia has been associated with a fascinating diversity of developmental and physiological processes. Despite the importance, much remains to be learned about the genetic control and cellular events that are involved in the differentiation of motile cilia. We also need to better understand the mechanisms by which cilia-driven fluid flow is able to influence such a variety of developmental and physiological processes. The Foxj1 family of proteins has now been definitively established as master regulators of motile ciliogenesis.1,2 Identification of the Kintoun/PF13 protein has shed light on the assembly of dynein arms,3 whereas live imaging of ciliary motility has led to the discovery of an intriguing new role for motile cilia in otolith formation in the ear.4.
Comment on
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The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos.Nat Genet. 2008 Dec;40(12):1454-60. doi: 10.1038/ng.267. Epub 2008 Nov 16. Nat Genet. 2008. PMID: 19011629 Free PMC article.
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Foxj1 transcription factors are master regulators of the motile ciliogenic program.Nat Genet. 2008 Dec;40(12):1445-53. doi: 10.1038/ng.263. Epub 2008 Nov 16. Nat Genet. 2008. PMID: 19011630
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Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.Nature. 2008 Dec 4;456(7222):611-6. doi: 10.1038/nature07471. Nature. 2008. PMID: 19052621 Free PMC article.
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