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Status |
Public on Dec 05, 2012 |
Title |
Interplay between HIV-1 infection and host microRNAs |
Platform organisms |
Homo sapiens; Mus musculus; Rattus norvegicus; Human alphaherpesvirus 1; Human betaherpesvirus 5; human gammaherpesvirus 4; JC polyomavirus; Human immunodeficiency virus 1; Human gammaherpesvirus 8; Betapolyomavirus hominis; Betapolyomavirus macacae |
Sample organism |
Homo sapiens |
Experiment type |
Non-coding RNA profiling by array
|
Summary |
Using microRNA array analyses of in vitro HIV-1-infected CD4+ cells, we find that several host microRNAs are significantly up- or downregulated around the time HIV-1 infection peaks in vitro. While microRNA-223 levels were significantly enriched in HIV-1-infected CD4+CD8− PBMCs, microRNA-29a/b, microRNA-155 and microRNA-21 levels were significantly reduced. Based on the potential for microRNA binding sites in a conserved sequence of the Nef-3′-LTR, several host microRNAs potentially could affect HIV-1 gene expression. Among those microRNAs, the microRNA-29 family has seed complementarity in the HIV-1 3′-UTR, but the potential suppressive effect of microRNA-29 on HIV-1 is severely blocked by the secondary structure of the target region. Our data support a possible regulatory circuit at the peak of HIV-1 replication which involves downregulation of microRNA-29, expression of Nef, the apoptosis of host CD4 cells and upregulation of microRNA-223.
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Overall design |
Time course of HIV infection on CD4 cells
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Contributor(s) |
Sun G, Li H, Wu X, Rossi J |
Citation(s) |
22080513 |
|
Submission date |
Dec 05, 2012 |
Last update date |
Jan 22, 2013 |
Contact name |
Xiwei Wu |
E-mail(s) |
xwu@coh.org
|
Organization name |
City of Hope National Medical Center
|
Department |
Computational and Quantitative Medicine
|
Street address |
1500 E. Duarte Rd.
|
City |
Duarte |
State/province |
CA |
ZIP/Postal code |
91010 |
Country |
USA |
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Platforms (1) |
GPL7724 |
miRCURY LNA microRNA Array, v. 9.2, all organisms |
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Samples (5)
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Relations |
BioProject |
PRJNA182981 |