Heterogenous nuclear ribonucleoprotein Q increases protein expression from HIV-1 Rev-dependent transcripts
Heterogenous nuclear ribonucleoprotein Q increases protein expression from HIV-1 Rev-dependent transcripts
Abstract Background Heterogenous nuclear ribonucleoproteins (hnRNPs) control many processes of the gene expression machinery including mRNA transcription, splicing, export, stability and translation. Recent data show interaction of the HIV-1 Rev regulatory protein with a subset of hnRNP proteins, that includes hnRNP Q, suggesting that hnRNPs can contribute to regulation of HIV-1 gene expression by Rev. Findings In this work we address the effect of hnRNP Q on Rev-dependent gene expression. We show that hnRNP Q overexpression increased levels of proteins produced from a Rev-dependent reporter gene in the presence of Rev. Increased protein levels did not correlate with changes in either the levels or the nucleocytoplasmic distribution of Rev-dependent reporter mRNAs. Similar observations were made in persistently HIV-1 infected HeLa cells. In these cells, hnRNP Q overexpression increased levels of the HIV-1 Gag-p24 protein, while levels of viral Rev-dependent mRNAs were not affected. Conclusion Our data indicate that hnRNP Q can stimulate the protein production of Rev-dependent mRNAs without changing mRNA levels and mRNA export, respectively. This suggests that hnRNP Q can boost HIV gene expression at the level of protein production.
- Helmholtz Zentrum München Germany
Gene Expression Regulation, Viral, Short Report, Epithelial Cells, rev Gene Products, Human Immunodeficiency Virus, Heterogeneous-Nuclear Ribonucleoproteins, Artificial Gene Fusion, Viral Proteins, Infectious Diseases, Genes, Reporter, Virology, Host-Pathogen Interactions, Humans, HeLa Cells
Gene Expression Regulation, Viral, Short Report, Epithelial Cells, rev Gene Products, Human Immunodeficiency Virus, Heterogeneous-Nuclear Ribonucleoproteins, Artificial Gene Fusion, Viral Proteins, Infectious Diseases, Genes, Reporter, Virology, Host-Pathogen Interactions, Humans, HeLa Cells
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