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RNA Biol. 2010 Sep-Oct;7(5):586-95. Epub 2010 Sep 1.

NcRNA-microchip analysis: a novel approach to identify differential expression of noncoding RNAs.

Author information

1
Division of Genomics and RNomics, Innsbruck Biocenter, Innsbruck Medical University, Innsbruck, Austria. Roland.Hutzinger@i-med.ac.at

Abstract

Epstein-Barr virus (EBV) infection of human B cells requires the presence of non-coding RNAs (ncRNAs), which regulate expression of viral and host genes. To identify differentially expressed regulatory ncRNAs involved in EBV infection, a specialized cDNA library, enriched for ncRNAs derived from EBV-infected cells, was subjected to deep-sequencing. From the deep-sequencing analysis, we generated a custom-designed ncRNA-microchip to investigate differential expression of ncRNA candidates. By this approach, we identified 25 differentially expressed novel host-encoded ncRNA candidates in EBV-infected cells, comprised of six non-repeat-derived and 19 repeat-derived ncRNAs. Upon EBV infection of B cells, we also observed increased expression levels of oncogenic miRNAs mir-221 and mir-222, which might contribute to EBV-related tumorigenesis, as well as decreased expression levels of RNase P RNA, a ribozyme involved in tRNA maturation. Thus, in this study we demonstrate that our ncRNA-microchip approach serves as a powerful tool to identify novel differentially expressed ncRNAs acting as potential regulators of gene expression during EBV infection.

PMID:
21037422
PMCID:
PMC3073255
[Indexed for MEDLINE]
Free PMC Article
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