| Literature DB >> 12421721 |
Shanming Liu1, Weining Lu, Tomoko Obara, Shiei Kuida, Jennifer Lehoczky, Ken Dewar, Iain A Drummond, David R Beier.
Abstract
The murine autosomal recessive juvenile cystic kidney (jck) mutation results in polycystic kidney disease. We have identified in jck mice a mutation in Nek8, a novel and highly conserved member of the Nek kinase family. In vitro expression of mutated Nek8 results in enlarged, multinucleated cells with an abnormal actin cytoskeleton. To confirm that a defect in the Nek8 gene can cause cystic disease, we performed a cross-species analysis: injection of zebrafish embryos with a morpholino anti-sense oligonucleotide corresponding to the ortholog of Nek8 resulted in the formation of pronephric cysts. These results demonstrate that comparative analysis of gene function in different model systems represents a powerful means to annotate gene function.Entities:
Mesh:
Substances:
Year: 2002 PMID: 12421721 DOI: 10.1242/dev.00173
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868