Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989 Apr;9(4):1721-32.
doi: 10.1128/mcb.9.4.1721-1732.1989.

Upstream activation sequence-dependent alteration of chromatin structure and transcription activation of the yeast GAL1-GAL10 genes

Affiliations

Upstream activation sequence-dependent alteration of chromatin structure and transcription activation of the yeast GAL1-GAL10 genes

M J Fedor et al. Mol Cell Biol. 1989 Apr.

Abstract

Conversion of the positioned nucleosome array characteristic of the repressed GAL1-GAL10 promoter region to the more accessible conformation of the induced state was found to depend on the upstream activation sequence, GAL4 protein, a positive regulator of transcription, and galactose, the inducing agent. The effect of the GAL4 protein-upstream activation sequence complex on the structure of adjacent chromatin required no other promoter sequences. Although sequences protected by histones in the repressed state became more accessible to micrococcal nuclease and (methidiumpropyl-EDTA)iron(II) cleavage following induction of transcription, DNA-protein particles containing these sequences retained the electrophoretic mobility of nucleosomes, indicating that the promoter region can be associated with nucleosomes under conditions of transcription activation.

PubMed Disclaimer

Similar articles

Cited by

References

    1. EMBO J. 1986 Oct;5(10):2689-96 - PubMed
    1. Mol Cell Biol. 1986 Jan;6(1):38-46 - PubMed
    1. Mol Cell Biol. 1986 Jul;6(7):2298-304 - PubMed
    1. J Mol Biol. 1986 Jul 20;190(2):177-90 - PubMed
    1. Cell. 1987 Jan 30;48(2):289-95 - PubMed

Publication types

MeSH terms