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PMID: 3128796 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Analysis of a DNase I-hypersensitive site in transgenic Drosophila reveals a key regulatory element of Sgs3.

Ramain P, Giangrande A, Richards G, Bellard M

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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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1988-04-00
Pages
2718-22
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC280070
Subset
IM
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