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

被引:163
作者
Liu, SM
Lu, WN
Obara, T
Kuida, S
Lehoczky, J
Dewar, K
Drummond, IA
Beier, DR [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Genet, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Renal Unit, Boston, MA 02114 USA
[3] MIT, Ctr Genome Res, Whitehead Inst Biomed Res, Cambridge, MA 02139 USA
来源
DEVELOPMENT | 2002年 / 129卷 / 24期
关键词
PKD; mouse models; zebrafish; Nek kinase;
D O I
10.1242/dev.00173
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:5839 / 5846
页数:8
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