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
Comparative Study
. 1991 Nov 15;88(22):10188-92.
doi: 10.1073/pnas.88.22.10188.

In vivo protein-DNA interactions at the beta-globin gene locus

Affiliations
Comparative Study

In vivo protein-DNA interactions at the beta-globin gene locus

T Ikuta et al. Proc Natl Acad Sci U S A. .

Abstract

We have investigated in vivo protein-DNA interactions in the beta-globin gene locus by dimethyl sulfate (DMS) footprinting in K562 cells, which express epsilon- and gamma-globin but not beta-globin. In the locus control region, hypersensitive site 2 (HS-2) exhibited footprints in several putative protein binding motifs. HS-3 was not footprinted. The beta promoter was also not footprinted, while extensive footprints were observed in the promoter of the active gamma-globin gene. No footprints were seen in the A gamma and beta 3' enhancers. With several motifs, additional protein interactions and alterations in binding patterns occurred with hemin induction. In HeLa cells, some footprints were observed in some of the motifs in HS-2, compatible with the finding that HS-2 has some enhancer function in HeLa cells, albeit much weaker than its activity in K562 cells. No footprint was seen in B lymphocytes. In vivo footprinting is a useful method for studying relevant protein-DNA interactions in erythroid cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Blood. 1975 Mar;45(3):321-34 - PubMed
    1. Genes Dev. 1991 Jun;5(6):919-31 - PubMed
    1. Methods Enzymol. 1980;65(1):499-560 - PubMed
    1. Proc Natl Acad Sci U S A. 1981 Jan;78(1):348-52 - PubMed
    1. Proc Natl Acad Sci U S A. 1984 Apr;81(7):1991-5 - PubMed

Publication types