| Literature DB >> 18287022 |
Terrence Town1, Joshua J Breunig, Matthew R Sarkisian, Charalampos Spilianakis, Albert E Ayoub, Xiuxin Liu, Anthony F Ferrandino, A Rachel Gallagher, Ming O Li, Pasko Rakic, Richard A Flavell.
Abstract
Cilia are present on nearly all cell types in mammals and perform remarkably diverse functions. However, the mechanisms underlying ciliogenesis are unclear. Here, we cloned a previously uncharacterized highly conserved gene, stumpy, located on mouse chromosome 7. Stumpy was ubiquitously expressed, and conditional loss in mouse resulted in complete penetrance of perinatal hydrocephalus (HC) and severe polycystic kidney disease (PKD). We found that cilia in stumpy mutant brain and kidney cells were absent or markedly deformed, resulting in defective flow of cerebrospinal fluid. Stumpy colocalized with ciliary basal bodies, physically interacted with gamma-tubulin, and was present along ciliary axonemes, suggesting that stumpy plays a role in ciliary axoneme extension. Therefore, stumpy is essential for ciliogenesis and may be involved in the pathogenesis of human congenital malformations such as HC and PKD.Entities:
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Year: 2008 PMID: 18287022 PMCID: PMC2268549 DOI: 10.1073/pnas.0712385105
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205