A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish

Author:

Liu Shanming1,Lu Weining1,Obara Tomoko2,Kuida Shiei1,Lehoczky Jennifer3,Dewar Ken3,Drummond Iain A.2,Beier David R.1

Affiliation:

1. Genetics Division, Brigham and Women's Hospital, Harvard Medical School,Boston, MA, USA

2. Renal Unit, Massachusetts General Hospital, Boston, MA, USA

3. Whitehead Institute for Biomedical Research/MIT Center for Genome Research,Cambridge, MA, USA

Abstract

The murine autosomal recessive juvenile cystic kidney (jck)mutation results in polycystic kidney disease. We have identified injck mice a mutation in Nek8, a novel and highly conserved member of the Nek kinase family. In vitro expression of mutated Nek8results 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 ofNek8 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.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

Reference38 articles.

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3. Atala, A., Freeman, M. R., Mandell, J. and Beier, D. R.(1993). Juvenile cystic kidneys (jck): a new mouse mutation which causes polycystic kidneys. Kidney Intl.43,1081-1085.

4. Cormack, B. (1998). Current protocols in molecular biology. In Current Protocols in Molecular Biology, Vol. 1 (ed. F. Ausubel, R. Brent,R. Kingston, D. Moore, J. Seidman, J. Smith and K. Struhl). New York: John Wiley and Sons.

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