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Open Access Research article

Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus

Helen J Blair1, Stuart Tompson12, Yu-Ning Liu1, Jennifer Campbell1, Katie MacArthur1, Chris P Ponting3, Victor L Ruiz-Perez4 and Judith A Goodship1*

Author affiliations

1 Institute of Human Genetics, Newcastle University, Centre for Life, Central Parkway, Newcastle Upon Tyne, NE1 3BZ, UK

2 Medical Genetics Institute, Cedars-Sinai Medical Center 8727 West Third Street, Suite 203, Los Angeles, CA 90048, USA

3 MRC Functional Genomics Unit, University of Oxford, Department of Physiology, Anatomy and Genetics, South Parks Road, Oxford, OX1 3QX, UK

4 Instituto de Investigaciones Biom├ędicas de Madrid (CSIC-UAM) and Ciber de enfermedades raras (Ciberer), Arturo Duperier, 4, 28029, Madrid, Spain

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Citation and License

BMC Biology 2011, 9:14  doi:10.1186/1741-7007-9-14

Published: 28 February 2011

Abstract

Background

Evc is essential for Indian Hedgehog (Hh) signalling in the cartilage growth plate. The gene encoding Evc2 is in close proximity in divergent orientation to Evc and mutations in both human genes lead to the chondrodysplasia Ellis-van Creveld syndrome.

Results

Bioinformatic analysis reveals that the Evc and Evc2 genes arose through a duplication event early in metazoan evolution and were subsequently lost in arthropods and nematodes. Here we demonstrate that Evc2 is essential for Hh pathway activation in response to the Smo agonist purmorphamine. A yeast two-hybrid screen using Evc as bait identified Evc2 as an Evc binding partner and we confirmed the interaction by immunoprecipitation. We developed anti-Evc2 antibodies and show that Evc2 and Evc co-localize at the basal body and also on primary cilia. In transfected cells, basal body and cilia localization is observed when Evc and Evc2 constructs are co-transfected but not when either construct is transfected individually. We show that Evc and Evc2 are cilia transmembrane proteins, the C-terminus for both being intracellular and Evc2, but not Evc, having an extracellular portion. Furthermore, Evc is absent at the basal body in Evc2 null cells. Using Western blots of cytoplasmic and nuclear protein, we also demonstrate that full length Evc2 but not Evc, is located in the nucleus.

Conclusions

We demonstrate for the first time that Evc2 is a positive regulator of the Hh signalling pathway and that it is located at the basal body of primary cilia. We show that the presence of Evc and Evc2 at the basal body and cilia membrane is co-dependent. In addition, Evc2, but not Evc, is present in the cell nucleus suggesting movement of Evc2 between the cilium and nucleus.