Inhibition of RNA splicing at the Rous sarcoma virus src 3' splice site is mediated by an interaction between a negative cis element and a chicken embryo fibroblast nuclear factor

Author:

Amendt B A1,Simpson S B1,Stoltzfus C M1

Affiliation:

1. Department of Microbiology, University of Iowa, Iowa City 52242, USA.

Abstract

In permissive Rous sarcoma virus-infected chicken embryo fibroblasts (CEF), approximately equimolar amounts of env and src mRNAs are present. In nonpermissive mammalian cells, the src mRNA level is elevated and env mRNA level is reduced. A cis element in the region between the env gene and the src 3' splice site, which we have termed the suppressor of src splicing (SSS), acts specifically in CEF but not in human cells to reduce src mRNA levels. The splicing inhibition in CEF is not caused by a base-paired structure which is predicted to form between the SSS and the src 3' splice site. To further investigate the mechanism of the inhibition, we have used human HeLa cell nuclear extracts to compare in vitro the rates of splicing of RNA substrates containing the Rous sarcoma virus major 5' splice site and either the env or src 3' splice sites. We show that the src 3' splice site is used approximately fivefold more efficiently than the env 3' splice site. The efficiency of in vitro splicing at the src 3' splice site is specifically reduced by addition of CEF nuclear extract. The inhibition is dependent on the presence of the SSS element and can be abrogated by addition of competitor RNA. We propose that the SSS region represents a binding site for a negative-acting CEF splicing factor(s).

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference39 articles.

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4. cis-acting regulatory elements within gag genes of avian retroviruses;Arrigo S.;Mol. Cell. Biol.,1987

5. Splicing of the alternative exons of the chicken, rat, and Xenopustropomyosin transcripts requires class-specific elements;Balvay L.;J. Biol. Chem.,1994

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