Abstract
We have undertaken chromatin studies on transformed Drosophila strains carrying DNA sequences modified in the region of the DNase I (EC 3.1.4.5)-hypersensitive sites -750 and -600 base pairs upstream from the Sgs3 start site. Although both sites are developmentally specific, modifications in the -750 site have little or no effect on Sgs3-encoded transcript levels, whereas either deletion or replacement of sequences at the -600 site causes an important reduction in transcript levels. The element associated with the -600 site enhances Sgs3 transcription when displaced with respect to the start site. This combined approach has defined sequence elements necessary both for normal transcript levels as well as the chromatin structure characteristic of Sgs3 activity in vivo.
MeSH Terms
Animals
Animals, Genetically Modified/genetics
Base Sequence
Chromatin/ultrastructure
DNA Mutational Analysis
Deoxyribonuclease I/metabolism
Drosophila melanogaster/genetics
Gene Expression Regulation
Genes, Regulator
Molecular Sequence Data
Regulatory Sequences, Nucleic Acid
Salivary Proteins and Peptides/genetics
Transcription, Genetic
Chemicals
Chromatin
Salivary Proteins and Peptides
Deoxyribonuclease I
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ramain P
Laboratoire de Génétique Moléculaire des Eucaryotes du Centre National de la Recherche Scientifique, Faculté de Médecine, Strasbourg, France.
Giangrande A
Richards G
Bellard M
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