期刊
AMERICAN JOURNAL OF HUMAN GENETICS
卷 95, 期 3, 页码 257-274出版社
CELL PRESS
DOI: 10.1016/j.ajhg.2014.08.005
关键词
-
资金
- NICHD [2R01HD048584]
- NHLBI [U01-HL098180]
- NRW Research School Cell Dynamics and Disease, CEDAD
- Deutsche Forschungsgemeinschaft [DFG OM 6/4]
- IZKF, Muenster [Om2/009/12]
- Schroder Stiftung
- Kindness for Kids
- SYSCILIA (EU) [241955]
- NWO [Vici-016.130.664]
- BESTCILIA (EU) [305404]
- Max Planck Society
- DFG [SFB629]
- European Union - Regional Development Fund
- Wellcome Trust [WT091310]
- Great Ormond Street Hospital Children's Charity
- Milena Carvajal Pro-Kartagener Foundation, Action Medical Research [GN2101]
- Newlife Foundation for Disabled Children UK [10-11/15]
- MRC [MR/L01629X/1]
- Wellcome Trust
- MRC [MR/L01629X/1] Funding Source: UKRI
- Action Medical Research [2101] Funding Source: researchfish
- Great Ormond Street Hospital Childrens Charity [V1299] Funding Source: researchfish
- Medical Research Council [MR/L01629X/1] Funding Source: researchfish
A diverse family of cytoskeletal dynein motors powers various cellular transport systems, including axonemal dyneins generating the force for ciliary and flagellar beating essential to movement of extracellular fluids and of cells through fluid. Multisubunit outer dynein arm (ODA) motor complexes, produced and preassembled in the cytosol, are transported to the ciliary or flagellar compartment and anchored into the axonemal microtubular scaffold via the ODA docking complex (ODA-DC) system. In humans, defects in ODA assembly are the major cause of primary ciliary dyskinesia (PCD), an inherited disorder of ciliary and flagellar dysmotility characterized by chronic upper and lower respiratory infections and defects in laterality. Here, by combined high-throughput mapping and sequencing, we identified CCDC151 loss-of-function mutations in five affected individuals from three independent families whose cilia showed a complete loss of ODAs and severely impaired ciliary beating. Consistent with the laterality defects observed in these individuals, we found Ccdc151 expressed in vertebrate left-right organizers. Homozygous zebrafish ccdc151(ts272a) and mouse Ccdc151(snb1) mutants display a spectrum of situs defects associated with complex heart defects. We demonstrate that CCDC151 encodes an axonemal coiled coil protein, mutations in which abolish assembly of CCDC151 into respiratory cilia and cause a failure in axonemal assembly of the ODA component DNAH5 and the ODA-DC-associated components CCDC114 and ARMC4. CCDC151-deficient zebrafish, planaria, and mice also display ciliary dysmotility accompanied by ODA loss. Furthermore, CCDC151 coimmunoprecipitates CCDC114 and thus appears to be a highly evolutionarily conserved ODA-DC-related protein involved in mediating assembly of both ODAs and their axonemal docking machinery onto ciliary microtubules.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据