Retrovirology

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Changes in microRNA expression profiles in HIV-1-transfected human cells

Man Lung Yeung1, Yamina Bennasser1, Timothy G Myers2, Guojian Jiang2, Monsef Benkirane3 and Kuan-Teh Jeang1,4*

Author Affiliations

1 Molecular Virology Section, Laboratory of Molecular Microbiology National Institute of Allergy and Infectious Diseases, National Institutes of Health Bethesda, Maryland 20892-0460, USA

2 Microarray Research Facility, Research Technologies Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health Bethesda, Maryland 20892-8005, USA

3 Laboratoire de Virologie Moleculaire, Institut de Genetique Humaine, CNRS UPR1142, Montpellier, France

4 Building 4, Room 306, 9000 Rockville Pike, Bethesda, MD 20892-0460, USA

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Retrovirology 2005, 2:81 doi:10.1186/1742-4690-2-81

Published: 28 December 2005

Abstract

MicroRNAs (miRNAs) are small RNAs of 18–25 nucleotides (nt) in length that play important roles in regulating a variety of biological processes. Recent studies suggest that cellular miRNAs may serve to control the replication of viruses in cells. If such is the case, viruses might be expected to evolve the ability to modulate the expression of cellular miRNAs. To ask if expression of HIV-1 genes changes the miRNA profiles in human cells, we employed a high throughput microarray method, termed the RNA-primed Array-based Klenow Enzyme (RAKE) assay. Here, we describe the optimization of this assay to quantify the expression of miRNAs in HIV-1 transfected human cells. We report distinct differences in miRNA profiles in mock-transfected HeLa cells versus HeLa cells transfected with an infectious HIV-1 molecular clone, pNL4-3.