Making Sense of Cilia in Disease: The Human Cilloplathies

被引:245
作者
Baker, Kate [1 ]
Beales, Philip L. [1 ]
机构
[1] UCL Inst Child Hlth, London WC1N 1EH, England
基金
英国医学研究理事会;
关键词
cilia; ciliopathy; OMIM; Bardet-Biedl; Joubert syndrome; BARDET-BIEDL-SYNDROME; RIB-POLYDACTYLY SYNDROME; ASPHYXIATING THORACIC DYSTROPHY; HEPATIC-PANCREATIC DYSPLASIA; JOUBERT-SYNDROME; ALSTROM-SYNDROME; MECKEL-SYNDROME; SYNDROME PROTEINS; INTRAFLAGELLAR TRANSPORT; CEREBELLAR DEVELOPMENT;
D O I
10.1002/ajmg.c.30231
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ubiquitous in nature, cilia and flagella comprise nearly identical structures with similar functions. The most obvious example of the latter is motility: driving movement of the organism or particle flow across the epithelial surface in fixed structures. In vertebrates, such motile cilia are evident in the respiratory epithelia, ependyma, and oviducts. For over a century, non-motile cilia have been observed on the surface of most vertebrate cells but until recently their function has eluded us. Gathering evidence now points to critical roles for the mono-cilium in sensing the extracellular environment, and perturbation of this function gives rise to a predictable panoply of clinical problems. We review the common clinical phenotypes associated with ciliopathies and interrogate Online Mendelian Inheritance in Man (OMIM) to compile a comprehensive list of putative disorders in which ciliary dysfunction may play a role. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:281 / 295
页数:15
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