Journal of Biological Chemistry · 2010 · 86 citations · 42 references
Life SciencesMicrobiologyMolecular BiologyGene ExpressionMolecular VirologyVirologyMacrophage BiologyMicrorna BiogenesisMicrorna BiologyMicrorna-mediated RegulationViral Gene ExpressionViral PathogenesisDicer Enzyme FunctionDicer ProcessingDicer-like EnzymesDicer-mediated ProcessingMicrorna Function In DifferentiationMicrorna In DifferentiationViral Gene SilencingViral Replication Control
MicroRNAs (miRNAs) are a class of small RNA molecules that function to control gene expression and restrict viral replication in host cells. The production of miRNAs is believed to be dependent upon the DICER enzyme. Available evidence suggests that in T lymphocytes, HIV-1 can both suppress and co-opt the host's miRNA pathway for its own benefit. In this study, we examined the state of miRNA production in monocytes and macrophages as well as the consequences of viral infection upon the production of miRNA. Monocytes in general express low amounts of miRNA-related proteins, and DICER in particular could not be detected until after monocytes were differentiated into macrophages. In the case where HIV-1 was present prior to differentiation, the expression of DICER was suppressed. MicroRNA chip results for RNA isolated from transfected and treated cells indicated that a drop in miRNA production coincided with DICER protein suppression in macrophages. We found that the expression of DICER in monocytes is restricted by miR-106a, but HIV-1 suppressed DICER expression via the viral gene Vpr. Additionally, analysis of miRNA expression in monocytes and macrophages revealed evidence that some miRNAs can be processed by both DICER and PIWIL4. Results presented here have implications for both the pathology of viral infections in macrophages and the biogenesis of miRNAs. First, HIV-1 suppresses the expression and function of DICER in macrophages via a previously unknown mechanism. Second, the presence of miRNAs in monocytes lacking DICER indicates that some miRNAs can be generated by proteins other than DICER.
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Konstantin D. Taganov, Mark Boldin, Kuang‐Jung Chang et al. · Proceedings of the National Academy of Sciences · 2006 · 4.3K citations · Full text
Jordan M. Cummins, Yiping He, Rebecca Leary et al. · Proceedings of the National Academy of Sciences · 2006 · 926 citations · Full text