Abstract

BackgroundHeterogenous 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.FindingsIn 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.ConclusionOur 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.

Highlights

  • Heterogenous nuclear ribonucleoproteins control many processes of the gene expression machinery including mRNA transcription, splicing, export, stability and translation

  • Our data indicate that Heterogenous nuclear ribonucleoproteins (hnRNPs) 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

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Summary

Introduction

Heterogenous nuclear ribonucleoproteins (hnRNPs) control many processes of the gene expression machinery including mRNA transcription, splicing, export, stability and translation. Similar results were obtained with a plasmid expressing hnRNP Q without the CYN-tag (data not shown), confirming the specific influence of hnRNP Q on reporter protein production. A hnRNP Q deletion mutant lacking the RGG domain from amino acids 444–623 (hnRNP Q-(Δ444-623)-CYN) was not able to boost reporter expression and did not bind Rev in exBIFC assays (Figure 1E).

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