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 Jun;8(6):1867-77.
doi: 10.1002/j.1460-2075.1989.tb03583.x.

A DNA binding protein that recognizes oligo(dA).oligo(dT) tracts

Affiliations

A DNA binding protein that recognizes oligo(dA).oligo(dT) tracts

E Winter et al. EMBO J. 1989 Jun.

Abstract

Oligo(dA).oligo(dT) tracts are common intergenic sequences in many organisms. In the yeast Saccharomyces cerevisiae, these sequences have been shown to influence transcription of adjacent genes. We have purified an oligo(dA).oligo(dT)-binding protein from S. cerevisiae and cloned its gene. This protein, which has been named datin, requires at least 9-11 bp of oligo(dA).oligo(dT) DNA for high affinity binding. The gene for datin (the DAT gene) encodes a 248-residue protein which contains a number of repeated sequence motifs. Datin purified from yeast corresponds to the N-terminal half of the DAT gene product. Null mutants in the DAT gene are viable but phenotypically distinguishable from congenic wild-type strains. We discuss unusual structural features and biochemical properties of datin in relation to its possible functions.

PubMed Disclaimer

Similar articles

Cited by

References

    1. FEBS Lett. 1985 Jan 28;180(2):275-9 - PubMed
    1. Cell. 1985 Jan;40(1):55-62 - PubMed
    1. Proc Natl Acad Sci U S A. 1985 Mar;82(6):1585-8 - PubMed
    1. Gene. 1985;33(1):103-19 - PubMed
    1. Cell. 1985 Dec;43(3 Pt 2):567-81 - PubMed

Publication types

MeSH terms

Associated data