PUBLICATION
Gli2a protein localization reveals a role for Iguana/DZIP1 in primary ciliogenesis and a dependence of Hedgehog signal transduction on primary cilia in the zebrafish
- Authors
- Kim, H.R., Richardson, J., van Eeden, F., and Ingham, P.W.
- ID
- ZDB-PUB-100525-11
- Date
- 2010
- Source
- BMC Biology 8: 65 (Journal)
- Registered Authors
- Ingham, Philip, Kim, Rosemary, van Eeden, Freek
- Keywords
- none
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Carrier Proteins/metabolism*
- Cilia/physiology*
- DNA Primers/genetics
- Embryo, Nonmammalian/metabolism
- Embryo, Nonmammalian/physiology
- Green Fluorescent Proteins/metabolism
- Hedgehog Proteins/metabolism*
- Immunohistochemistry
- In Situ Hybridization
- Molecular Sequence Data
- Recombinant Fusion Proteins/metabolism
- Sequence Analysis, DNA
- Signal Transduction/physiology*
- Transcription Factors/metabolism*
- Zebrafish
- Zebrafish Proteins/metabolism*
- PubMed
- 20487519 Full text @ BMC Biol.
Citation
Kim, H.R., Richardson, J., van Eeden, F., and Ingham, P.W. (2010) Gli2a protein localization reveals a role for Iguana/DZIP1 in primary ciliogenesis and a dependence of Hedgehog signal transduction on primary cilia in the zebrafish. BMC Biology. 8:65.
Abstract
BACKGROUND: In mammalian cells, the integrity of the primary cilium is critical for proper regulation of the Hedgehog (Hh) signal transduction pathway. Whether or not this dependence on the primary cilium is a universal feature of vertebrate Hedgehog signalling has remained contentious due, in part, to the apparent divergence of the intracellular transduction pathway between mammals and teleost fish. RESULTS: Here, using a functional Gli2-GFP fusion protein, we show that, as in mammals, the Gli2 transcription factor localizes to the primary cilia of cells in the zebrafish embryo and that this localization is modulated by the activity of the Hh pathway. Moreover, we show that the Igu/DZIP1protein, previously implicated in the modulation of Gli activity in zebrafish, also localizes to the primary cilium and is required for its proper formation. CONCLUSION: Our findings demonstrate a conserved role of the primary cilium in mediating Hedgehog signalling activity across the vertebrate phylum and validate the use of the zebrafish as a representative model for the in vivo analysis of vertebrate Hedgehog signalling.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping