Interactome of the HIV-1 proteome and human host RNA

The human immunodeficiency virus (HIV-1) is highly dependent on a variety of host factors. Beside proteins, host RNA molecules are reported to aid HIV-1 replication and latency maintenance. Here, we implement multiple workflows of native RNA immunoprecipitation and sequencing (nRIPseq) to determine direct host RNA interaction partners of all 18 HIV-1 (poly)proteins. We identify 1,727 HIV-1 protein - human RNA interactions in the Jurkat cell line and 1,558 interactions in SupT1 cells for a subset of proteins, and discover distinct cellular pathways that seem to be used or controlled by HIV-1 on the RNA level: Tat binds mRNAs of proteins involved in the super elongation complex (AFF1-4, Cyclin-T1). Correlation of the interaction scores (based on binding abundancy) allows identifying the highest confidence interactions, for which we perform a small-scale knockdown screen that leads to the identification of three HIV-1 protein binding RNA interactors involved in HIV-1 replication (AFF2, H4C9 and RPLP0).

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Publication Details

Journal
EMBO Reports
Published
2024-08-09
DOI
https://doi.org/10.1038/s44319-024-00222-6
Citations
3
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.70

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article

Interactome of the HIV-1 proteome and human host RNA

Wim Trypsteen, Kimberly Verniers, Nevan J. Krogan, Tinus Schynkel et al.
3 citations
EMBO Reports
RNA modifications and cancer
0.70
article

Interactome of the HIV-1 proteome and human host RNA

Wim Trypsteen, Kimberly Verniers, Nevan J. Krogan, Tinus Schynkel, Gwendolyn Μ. Jang, Pieter Mestdagh, Willem van Snippenberg, Linos Vandekerckhove
article en
3 citations

Abstract

The human immunodeficiency virus (HIV-1) is highly dependent on a variety of host factors. Beside proteins, host RNA molecules are reported to aid HIV-1 replication and latency maintenance. Here, we implement multiple workflows of native RNA immunoprecipitation and sequencing (nRIPseq) to determine direct host RNA interaction partners of all 18 HIV-1 (poly)proteins. We identify 1,727 HIV-1 protein - human RNA interactions in the Jurkat cell line and 1,558 interactions in SupT1 cells for a subset of proteins, and discover distinct cellular pathways that seem to be used or controlled by HIV-1 on the RNA level: Tat binds mRNAs of proteins involved in the super elongation complex (AFF1-4, Cyclin-T1). Correlation of the interaction scores (based on binding abundancy) allows identifying the highest confidence interactions, for which we perform a small-scale knockdown screen that leads to the identification of three HIV-1 protein binding RNA interactors involved in HIV-1 replication (AFF2, H4C9 and RPLP0).

EMBO ReportsVol. 25(9)
Gladstone Institutes (US), University of California, San Francisco (US), Ghent University Hospital (BE), Quantitative BioSciences (US), VIB-UGent Center for Medical Biotechnology (BE)
ViiV Healthcare, Fonds Wetenschappelijk Onderzoek, Universiteit Gent, Vlaamse regering
Good health and well-being
Openalex Percentile: Top 30%
RNA modifications and cancer
0.70
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Interactome of the HIV-1 proteome and human host RNA — Wim Trypsteen, Kimberly Verniers, et al. · EMBO Reports (2024) | TGRS Research Map | TGRS