The retrotransposonCopiacontrols the relative levels of its gene products post-transcriptionally be differential expression from its two major mRNAs
- 1 January 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 18 (10) , 2947-2951
- https://doi.org/10.1093/nar/18.10.2947
Abstract
All retroviruses and retrotransposons studied to date regulate the relative levels of gag and pol/int gene products post-transcriptionally from a single mRNA. In these genetic elements the production of protein encoded by the pol and int genes is attenuated by a translational stop or frameshift in the reading frame preceding their coding regions in the mRNA. We show here that the Drosophila retrotransposon copia also produces lower amounts of gene products from its int/pol region than gag region but this is achieved by a mechanism which is novel for this class of genetic element. We show by the use of gene fusion constructs that the subgenomic 2 kilobase copia RNA, encoding gag products, is expressed as protein in cultured cells at least ten-fold more efficiently than the full genome length RNA, which additionally contains the pol and int open reading frames.This publication has 30 references indexed in Scilit:
- Regulatory pathways governing HIV-1 replicationPublished by Elsevier ,1989
- Tnt1, a mobile retroviral-like transposable element of tobacco isolated by plant cell geneticsNature, 1989
- A copia-like transposable element family in Arabidopsis thalianaNature, 1988
- Characterization of ribosomal frameshifting in HIV-1 gag-pol expressionNature, 1988
- Sequence requirements for splicing of higher eukaryotic nuclear pre-mRNACell, 1986
- The trans-activator gene of the human T cell lymphotropic virus type III is required for replicationCell, 1986
- The nucleotide sequences of copia and copia-related RNA in Drosophila virus-like particlesNature, 1985
- A retrovirus-like strategy for expression of a fusion protein encoded by yeast transposon Ty1Nature, 1985
- A minimal intron length but no specific internal sequence is required for splicing the large rabbit β-globin intronCell, 1984
- Analysis of transcripts from two families of nomadic DNAJournal of Molecular Biology, 1982