Abstract
The glass gene is required for proper photo-receptor differentiation during development of the Drosophila eye glass codes for a DNA-binding protein containing five zinc fingers that we show is a transcriptional activator. A comparison of the sequences of the glass genes from two species of Drosophila and a detailed functional domain analysis of the Drosophila melanogaster glass gene reveal that both the DNA-binding domain and the transcriptional-activation domain are highly conserved between the two species. Analysis of the DNA-binding domain of glass indicates that the three carboxyl-terminal zinc fingers alone are necessary and sufficient for DNA binding. We also show that a deletion mutant of glass containing only the DNA-binding domain can behave in a dominant-negative manner both in vivo and in a cell culture assay that measures transcriptional activation.
Publication types
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Comparative Study
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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Binding Sites
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Cell Line
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Chloramphenicol O-Acetyltransferase / analysis
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Chloramphenicol O-Acetyltransferase / biosynthesis
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DNA / metabolism
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DNA-Binding Proteins / biosynthesis*
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism
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Drosophila / genetics
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Drosophila / metabolism*
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Drosophila Proteins*
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Drosophila melanogaster / genetics
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Drosophila melanogaster / metabolism*
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Eye / ultrastructure
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Gene Expression
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Genes, Insect
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Microscopy, Electron, Scanning
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Molecular Sequence Data
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Oligodeoxyribonucleotides
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Sequence Homology, Amino Acid
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Trans-Activators / biosynthesis
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Trans-Activators / metabolism
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Transcription Factors / biosynthesis*
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Transcription, Genetic
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Transfection
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Zinc Fingers*
Substances
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DNA-Binding Proteins
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Drosophila Proteins
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Oligodeoxyribonucleotides
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Trans-Activators
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Transcription Factors
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gl protein, Drosophila
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DNA
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Chloramphenicol O-Acetyltransferase