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
. 1987 Dec;84(23):8306-10.
doi: 10.1073/pnas.84.23.8306.

A poly(A) addition site and a downstream termination region are required for efficient cessation of transcription by RNA polymerase II in the mouse beta maj-globin gene

Affiliations

A poly(A) addition site and a downstream termination region are required for efficient cessation of transcription by RNA polymerase II in the mouse beta maj-globin gene

J Logan et al. Proc Natl Acad Sci U S A. 1987 Dec.

Abstract

Sequence elements within the mouse beta maj-globin transcription unit required for efficient termination of transcription by RNA polymerase II have been delineated. To facilitate nascent-chain analysis of termination, the DNA segment in which transcription ceases was introduced into the adenovirus chromosome within its E1A transcription unit. Two beta-globin DNA elements were required to effect efficient termination: an upstream sequence that includes two poly(A) addition signals and a downstream region previously shown to be where RNA synthesis stops. The role of poly(A) addition in termination was established by introduction of several single base pair substitutions into the AATAAA polyadenylylation motifs. These mutations inhibited both polyadenylylation and termination within the beta-globin DNA segment. Therefore, poly(A) addition appears to be a prerequisite for efficient termination.

PubMed Disclaimer

References

    1. J Gen Virol. 1977 Jul;36(1):59-74 - PubMed
    1. Mol Cell Biol. 1984 Dec;4(12):2921-4 - PubMed
    1. Cell. 1978 Dec;15(4):1125-32 - PubMed
    1. Cell. 1978 Dec;15(4):1477-93 - PubMed
    1. Nature. 1979 Mar 22;278(5702):367-70 - PubMed

Publication types

LinkOut - more resources