
doi: 10.1038/nature02093
pmid: 14628052
The Eyes absent proteins are members of a conserved regulatory network implicated in the development of the eye, muscle, kidney and ear. Mutations in the Eyes absent genes have been associated with several congenital disorders including the multi-organ disease bronchio-oto-renal syndrome, congenital cataracts and late-onset deafness. On the basis of previous analyses it has been shown that Eyes absent is a nuclear transcription factor, acting through interaction with homeodomain-containing Sine oculis (also known as Six) proteins. Here we show that Eyes absent is also a protein tyrosine phosphatase. It does not resemble the classical tyrosine phosphatases that use cysteine as a nucleophile and proceed by means of a thiol-phosphate intermediate. Rather, Eyes absent is the prototype for a class of protein tyrosine phosphatases that use a nucleophilic aspartic acid in a metal-dependent reaction. Furthermore, the phosphatase activity of Eyes absent contributes to its ability to induce eye formation in Drosophila.
Molecular Sequence Data, Eye, Substrate Specificity, Drosophila melanogaster, Mutation, Animals, Drosophila Proteins, Amino Acid Sequence, Phosphorylation, Protein Tyrosine Phosphatases, Eye Proteins
Molecular Sequence Data, Eye, Substrate Specificity, Drosophila melanogaster, Mutation, Animals, Drosophila Proteins, Amino Acid Sequence, Phosphorylation, Protein Tyrosine Phosphatases, Eye Proteins
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