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 Dec;9(12):5298-304.
doi: 10.1128/mcb.9.12.5298-5304.1989.

Functional distinctions between yeast TATA elements

Affiliations

Functional distinctions between yeast TATA elements

P A Harbury et al. Mol Cell Biol. 1989 Dec.

Abstract

Although the yeast his3 promoter region contains two functional TATA elements, TR and TC, the GCN4 and GAL4 upstream activator proteins stimulate transcription only through TR. In combination with GAL4, an oligonucleotide containing the sequence TATAAA is fully sufficient for TR function, whereas almost all single-base-pair substitutions of this sequence abolish the ability of this element to activate transcription. Further analysis of these and other mutations of the TR element led to the following conclusions. First, sequences downstream of the TATAAA sequence are important for TR function. Second, a double mutant, TATTTA, can serve as a TR element even though the corresponding single mutation, TATTAA, is unable to do so. Third, three mutations have the novel property of being able to activate transcription in combination with GCN4 but not with GAL4; this finding suggests that activation by GCN4 and by GAL4 may not occur by identical mechanisms. From these observations, we address the question of whether there is a single TATA-binding factor required for the transcription of all genes.

PubMed Disclaimer

References

    1. Annu Rev Biochem. 1988;57:839-72 - PubMed
    1. Cell. 1988 Sep 23;54(7):931-42 - PubMed
    1. Nature. 1981 Nov 19;294(5838):217-23 - PubMed
    1. Nature. 1983 Feb 24;301(5902):680-6 - PubMed
    1. Cell. 1984 Feb;36(2):357-69 - PubMed

Publication types

LinkOut - more resources