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Dynamic Regulation of HIV-1 MRNA Populations Analyzed by Single-molecule Enrichment and Long-read Sequencing

Overview
Specialty Biochemistry
Date 2012 Aug 28
PMID 22923523
Citations 84
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Abstract

Alternative RNA splicing greatly expands the repertoire of proteins encoded by genomes. Next-generation sequencing (NGS) is attractive for studying alternative splicing because of the efficiency and low cost per base, but short reads typical of NGS only report mRNA fragments containing one or few splice junctions. Here, we used single-molecule amplification and long-read sequencing to study the HIV-1 provirus, which is only 9700 bp in length, but encodes nine major proteins via alternative splicing. Our data showed that the clinical isolate HIV-1(89.6) produces at least 109 different spliced RNAs, including a previously unappreciated ∼1 kb class of messages, two of which encode new proteins. HIV-1 message populations differed between cell types, longitudinally during infection, and among T cells from different human donors. These findings open a new window on a little studied aspect of HIV-1 replication, suggest therapeutic opportunities and provide advanced tools for the study of alternative splicing.

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References
1.
Asang C, Hauber I, Schaal H . Insights into the selective activation of alternatively used splice acceptors by the human immunodeficiency virus type-1 bidirectional splicing enhancer. Nucleic Acids Res. 2008; 36(5):1450-63. PMC: 2275126. DOI: 10.1093/nar/gkm1147. View

2.
Almarza D, Bussadori G, Navarro M, Mavilio F, Larcher F, Murillas R . Risk assessment in skin gene therapy: viral-cellular fusion transcripts generated by proviral transcriptional read-through in keratinocytes transduced with self-inactivating lentiviral vectors. Gene Ther. 2011; 18(7):674-81. DOI: 10.1038/gt.2011.12. View

3.
Llorian M, Smith C . Decoding muscle alternative splicing. Curr Opin Genet Dev. 2011; 21(4):380-7. DOI: 10.1016/j.gde.2011.03.006. View

4.
Sheth N, Roca X, Hastings M, Roeder T, Krainer A, Sachidanandam R . Comprehensive splice-site analysis using comparative genomics. Nucleic Acids Res. 2006; 34(14):3955-67. PMC: 1557818. DOI: 10.1093/nar/gkl556. View

5.
Bakkour N, Lin Y, Maire S, Ayadi L, Mahuteau-Betzer F, Nguyen C . Small-molecule inhibition of HIV pre-mRNA splicing as a novel antiretroviral therapy to overcome drug resistance. PLoS Pathog. 2007; 3(10):1530-9. PMC: 2042022. DOI: 10.1371/journal.ppat.0030159. View