Defects in ciliary localization of Nek8 is associated with cystogenesis

Mutations in the human NIMA (Never in Mitosis gene A)-related kinase 8 (Nek8) are associated with a rare form of the juvenile renal cystic disease, nephronophthisis type 9, and mutations in murine Nek8 cause renal cysts in jck mice. Cystogenesis involves dysfunctional ciliary signaling, and we have...

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Published in:Pediatric nephrology (Berlin, West) West), 2008-03, Vol.23 (3), p.377-387
Main Authors: Trapp, Melissa L., Galtseva, Alevtina, Manning, Danielle K., Beier, David R., Rosenblum, Norman D., Quarmby, Lynne M.
Format: Article
Language:English
Subjects:
Animals
Cell cycle
Cilia - genetics
Cilia - metabolism
Cyclin-dependent kinases
Cysts
Hospitals
Kidney - embryology
Kidney diseases
Kidney Tubules - metabolism
Kinases
Localization
Medicine
Medicine & Public Health
Mice
Mutation
Nephrology
NIMA-Related Kinases
Original Article
Pediatrics
Polycystic Kidney Diseases - genetics
Protein Kinases - biosynthesis
Protein Kinases - genetics
Protein-Serine-Threonine Kinases
Urology
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Summary:Mutations in the human NIMA (Never in Mitosis gene A)-related kinase 8 (Nek8) are associated with a rare form of the juvenile renal cystic disease, nephronophthisis type 9, and mutations in murine Nek8 cause renal cysts in jck mice. Cystogenesis involves dysfunctional ciliary signaling, and we have previously reported that Nek8 localizes to the primary cilium in mouse kidney epithelial cells. We now report that in developing mouse kidney, Nek8 is detected in the cilia of a subset of ureteric-bud-derived tubules at embryonic day (E)15.5. An increasing proportion of ureteric-bud-derived tubules express ciliary Nek8 until E18.5. Postnatal day 1 and 7 Nek8 is observed with equal frequency in both ureteric-bud and non-ureteric-bud-derived tubules. To investigate the cell biological consequences of kinase-deficient and jck mutant forms of Nek8, we transiently expressed green fluorescent protein (GFP)-tagged constructs in vitro. Mutations in the kinase and C-terminal domains of Nek8 adversely affected ciliary targeting but did not affect ciliogenesis or ciliary length. Consistent with these in vitro observations, kidneys from homozygous jck mice revealed reduced ciliary expression of Nek8 compared with kidneys from heterozygous (unaffected) mice. These data indicate that the ciliary localization of Nek8 in a subset of ureteric-bud-derived kidney tubules is essential for maintaining the integrity of those tubules in the mammalian kidney.
ISSN:0931-041X
1432-198X
DOI:10.1007/s00467-007-0692-y