Source:http://linkedlifedata.com/resource/pubmed/id/20181707
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2010-4-7
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pubmed:abstractText |
Certain viruses use microRNAs (miRNAs) to regulate the expression of their own genes, host genes, or both. Previous studies have identified a limited number of miRNAs expressed by herpes simplex viruses 1 and 2 (HSV-1 and -2), some of which are conserved between these two viruses. To more comprehensively analyze the miRNAs expressed by HSV-1 or HSV-2 during productive and latent infection, we applied a massively parallel sequencing approach. We were able to identify 16 and 17 miRNAs expressed by HSV-1 and HSV-2, respectively, including all previously known species, and a number of previously unidentified virus-encoded miRNAs. The genomic positions of most miRNAs encoded by these two viruses are within or proximal to the latency-associated transcript region. Nine miRNAs are conserved in position and/or sequence, particularly in the seed region, between these two viruses. Interestingly, we did not detect an HSV-2 miRNA homolog of HSV-1 miR-H1, which is highly expressed during productive infection, but we did detect abundant expression of miR-H6, whose seed region is conserved with HSV-1 miR-H1 and might represent a functional analog. We also identified a highly conserved miRNA family arising from the viral origins of replication. In addition, we detected several pairs of complementary miRNAs and we found miRNA-offset RNAs (moRs) arising from the precursors of HSV-1 and HSV-2 miR-H6 and HSV-2 miR-H4. Our results reveal elements of miRNA conservation and divergence that should aid in identifying miRNA functions.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/H60017115,
http://linkedlifedata.com/resource/pubmed/grant/H6003224,
http://linkedlifedata.com/resource/pubmed/grant/H600423,
http://linkedlifedata.com/resource/pubmed/grant/H6004756,
http://linkedlifedata.com/resource/pubmed/grant/H6004825,
http://linkedlifedata.com/resource/pubmed/grant/P01 NS35138,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI26126
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1098-5514
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4659-72
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pubmed:dateRevised |
2010-11-2
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pubmed:meshHeading |
pubmed-meshheading:20181707-Animals,
pubmed-meshheading:20181707-Cell Line,
pubmed-meshheading:20181707-Cercopithecus aethiops,
pubmed-meshheading:20181707-Conserved Sequence,
pubmed-meshheading:20181707-Herpesvirus 1, Human,
pubmed-meshheading:20181707-Herpesvirus 2, Human,
pubmed-meshheading:20181707-Humans,
pubmed-meshheading:20181707-MicroRNAs,
pubmed-meshheading:20181707-Polymorphism, Genetic,
pubmed-meshheading:20181707-RNA, Viral,
pubmed-meshheading:20181707-Sequence Analysis, DNA
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pubmed:year |
2010
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pubmed:articleTitle |
Numerous conserved and divergent microRNAs expressed by herpes simplex viruses 1 and 2.
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pubmed:affiliation |
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 250 Longwood Ave., Boston, MA 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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