A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium

Hum Mutat. 2014 Jan;35(1):137-46. doi: 10.1002/humu.22470.


Joubert syndrome (JS) is characterized by a distinctive cerebellar structural defect, namely the << molar tooth sign >>. JS is genetically heterogeneous, involving 20 genes identified to date, which are all required for cilia biogenesis and/or function. In a consanguineous family with JS associated with optic nerve coloboma, kidney hypoplasia, and polydactyly, combined exome sequencing and mapping identified a homozygous splice-site mutation in PDE6D, encoding a prenyl-binding protein. We found that pde6d depletion in zebrafish leads to renal and retinal developmental anomalies and wild-type but not mutant PDE6D is able to rescue this phenotype. Proteomic analysis identified INPP5E, whose mutations also lead to JS or mental retardation, obesity, congenital retinal dystrophy, and micropenis syndromes, as novel prenyl-dependent cargo of PDE6D. Mutant PDE6D shows reduced binding to INPP5E, which fails to localize to primary cilia in patient fibroblasts and tissues. Furthermore, mutant PDE6D is unable to bind to GTP-bound ARL3, which acts as a cargo-release factor for PDE6D-bound INPP5E. Altogether, these results indicate that PDE6D is required for INPP5E ciliary targeting and suggest a broader role for PDE6D in targeting other prenylated proteins to the cilia. This study identifies PDE6D as a novel JS disease gene and provides the first evidence of prenyl-binding-dependent trafficking in ciliopathies.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-Ribosylation Factors / metabolism
  • Abnormalities, Multiple
  • Animals
  • Cerebellar Diseases / genetics*
  • Cerebellar Diseases / metabolism*
  • Cerebellum / abnormalities
  • Cilia / metabolism*
  • Cyclic Nucleotide Phosphodiesterases, Type 6 / genetics*
  • Cyclic Nucleotide Phosphodiesterases, Type 6 / metabolism*
  • Exome
  • Eye Abnormalities / genetics*
  • Eye Abnormalities / metabolism*
  • Female
  • Genetic Predisposition to Disease
  • Homozygote
  • Humans
  • Kidney Diseases, Cystic / genetics*
  • Kidney Diseases, Cystic / metabolism*
  • Male
  • Models, Molecular
  • Pedigree
  • Phosphoric Monoester Hydrolases / genetics*
  • Phosphoric Monoester Hydrolases / metabolism*
  • Protein Prenylation
  • Proteomics
  • Retina / abnormalities*
  • Retina / metabolism
  • Sequence Analysis, DNA
  • Zebrafish / abnormalities
  • Zebrafish / genetics
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism


  • Zebrafish Proteins
  • Phosphoric Monoester Hydrolases
  • phosphoinositide 5-phosphatase
  • PDE6D protein, human
  • Cyclic Nucleotide Phosphodiesterases, Type 6
  • ADP-Ribosylation Factors
  • ARL3 protein, human

Supplementary concepts

  • Agenesis of Cerebellar Vermis