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EYA4, a novel vertebrate gene related to Drosophila eyes absent

Authors :
Kay Metcalfe
Alison Brown
Veronica van Heyningen
Robin M. Winter
Alessandro Bulfone
Marie Robertson
Alessandro DeGrandi
Sandro Banfi
Dian Donnai
Andrea Ballabio
Giuseppe Borsani
Isabel M. Hanson
Loris Bernard
Claudio Gattuso
Richard Axton
Margherita Mariani
Michael J. Dixon
Borsani, G
Degrandi, A
Ballabio, A
Bulfone, A
Bernard, L
Banfi, Sandro
Gattuso, C
Mariani, M
Dixon, M
Donnai, D
Metcalfe, K
Winter, R
Robertson, M
Axton, R
Brown, A
van Heyningen, V
Hanson, I.
Source :
Human Molecular Genetics. 8:11-23
Publication Year :
1999
Publisher :
Oxford University Press (OUP), 1999.

Abstract

We have isolated a family of four vertebrate genes homologous to eyes absent (eya), a key regulator of ocular development in Drosophila. Here we present the detailed characterization of the EYA4 gene in human and mouse. EYA4 encodes a 640 amino acid protein containing a highly conserved C-terminal domain of 271 amino acids which in Drosophila eya is known to mediate developmentally important protein-protein interactions. Human EYA4 maps to 6q23 and mouse Eya4 maps to the predicted homology region near the centromere of chromosome 10. In the developing mouse embryo, Eya4 is expressed primarily in the craniofacial mesenchyme, the dermamyotome and the limb. On the basis of map position and expression pattern, EYA4 is a candidate for oculo-dento-digital (ODD) syndrome, but no EYA4 mutations were found in a panel of ODD patients.

Details

ISSN :
14602083
Volume :
8
Database :
OpenAIRE
Journal :
Human Molecular Genetics
Accession number :
edsair.doi.dedup.....3794d67e8444628e9cc197cebf945fb4