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Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.

Authors :
Lu H
Galeano MCR
Ott E
Kaeslin G
Kausalya PJ
Kramer C
Ortiz-Brüchle N
Hilger N
Metzis V
Hiersche M
Tay SY
Tunningley R
Vij S
Courtney AD
Whittle B
Wühl E
Vester U
Hartleben B
Neuber S
Frank V
Little MH
Epting D
Papathanasiou P
Perkins AC
Wright GD
Hunziker W
Gee HY
Otto EA
Zerres K
Hildebrandt F
Roy S
Wicking C
Bergmann C
Source :
Nature genetics [Nat Genet] 2017 Jul; Vol. 49 (7), pp. 1025-1034. Date of Electronic Publication: 2017 May 22.
Publication Year :
2017

Abstract

Autosomal recessive polycystic kidney disease (ARPKD), usually considered to be a genetically homogeneous disease caused by mutations in PKHD1, has been associated with ciliary dysfunction. Here, we describe mutations in DZIP1L, which encodes DAZ interacting protein 1-like, in patients with ARPKD. We further validated these findings through loss-of-function studies in mice and zebrafish. DZIP1L localizes to centrioles and to the distal ends of basal bodies, and interacts with septin2, a protein implicated in maintenance of the periciliary diffusion barrier at the ciliary transition zone. In agreement with a defect in the diffusion barrier, we found that the ciliary-membrane translocation of the PKD proteins polycystin-1 and polycystin-2 is compromised in DZIP1L-mutant cells. Together, these data provide what is, to our knowledge, the first conclusive evidence that ARPKD is not a homogeneous disorder and further establish DZIP1L as a second gene involved in ARPKD pathogenesis.

Details

Language :
English
ISSN :
1546-1718
Volume :
49
Issue :
7
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
28530676
Full Text :
https://doi.org/10.1038/ng.3871