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Alternative DNA-protein interactions in variable-length internucleosomal regions associated withDrosophila Adhdistal promoter expression
Author(s) -
Amy Ewel,
Jeffrey R. Jackson,
Cheeptip Benyajati
Publication year - 1990
Publication title -
nucleic acids research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/18.7.1771
Subject(s) - biology , genetics , dna , microbiology and biotechnology , drosophila (subgenus) , drosophilidae , drosophila melanogaster , gene expression , gene
Chromatin at the Drosophila Adh distal promoter displays an ordered but different conformation in different cell types as detected by a modified exonuclease protection assay and accessibility to endonucleases. In cells not transcribing Adh (ADH-) sequences between -40 to +30 of the distal RNA initiation site exist as a DNA linker between positioned nucleosomes, and appear to interact with a specific DNA-binding protein. In contrast, a longer linker DNA, from -140 to +30, is bound in a multi-protein transcription initiation complex in cells that specifically transcribe the distal (adult) ADH RNA (ADH+A). These DNA-protein interactions can account for a localized open chromatin structure at the distal promoter in ADH+A cells. The observed mutually exclusive patterns of DNA-protein interactions in the linkers of different ADH cell types between -40 to +30 suggest a model for organizing alternative chromatin structure associated with gene regulation. Two DNA binding proteins, one being a TATA box binding factor, compete for overlapping sites to allow either assembly of a transcription initiation complex and transcription, or positioning of nucleosomes for stable repression.

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