Abstract
Cell proliferation and cell type specification are coordinately regulated during normal development. Cyclin E, a key G1/S cell cycle regulator, is regulated by multiple tissue-specific enhancers resulting in dynamic expression during Drosophila development. Here, we further characterized the enhancer that regulates cyclin E expression in the developing peripheral nervous system (PNS) and show that multiple sequence elements are required for the full cyclin E PNS enhancer activity. We further show that Wg signaling is important for the expression of cyclin E in the sensory organ precursor (SOP) cells through two conserved TCF binding sites. Blocking Wg signaling does not completely block SOP cell formation but does completely block SOP cell proliferation as well as the subsequent differentiation.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Base Sequence
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Binding Sites
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Cell Differentiation
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Cell Proliferation
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Conserved Sequence
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Cyclin E / genetics*
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Drosophila Proteins / metabolism*
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Drosophila melanogaster / cytology
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Drosophila melanogaster / embryology
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Drosophila melanogaster / genetics*
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Embryo, Nonmammalian / cytology
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Embryo, Nonmammalian / metabolism
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Embryonic Stem Cells / cytology*
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Embryonic Stem Cells / metabolism
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Enhancer Elements, Genetic / genetics
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Gene Expression Regulation, Developmental*
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Genes, Reporter
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Green Fluorescent Proteins / metabolism
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Molecular Sequence Data
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Peripheral Nervous System / cytology
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Peripheral Nervous System / embryology*
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Peripheral Nervous System / metabolism
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Sequence Deletion
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Signal Transduction*
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TCF Transcription Factors / metabolism
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Wnt1 Protein / metabolism*
Substances
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Cyclin E
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Drosophila Proteins
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TCF Transcription Factors
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Wnt1 Protein
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wg protein, Drosophila
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Green Fluorescent Proteins