Two alternating structures of the HIV-1 leader RNA
Open accessAbstract
In this study we demonstrate that the HIV-1 leader RNA exists in two alternative conformations, a branched structure consisting of several well-known hairpin motifs and a more stable structure that is formed by extensive long-distance base pairing. The latter conformation was first identified as a compactly folded RNA that migrates unusually fast in nondenaturing gels. The minimally required domains for formation of this conformer were determined by mutational analysis. The poly(A) and DIS regions of the leader are the major determinants of this RNA conformation. Further biochemical characterization of this conformer revealed that both hairpins are disrupted to allow extensive long-distance base pairing. As the DIS hairpin is known to be instrumental for formation of the HIV-1 RNA dimer, the interplay between formation of the conformer and dimerization was addressed. Formation of the conformer and the RNA dimer are mutually exclusive. Consequently, the conformer must rearrange into a branched structure that exposes the dimer initiation signal (DIS) hairpin, thus triggering formation of the RNA dimer. This structural rearrangement is facilitated by the viral nucleocapsid protein NC. We propose that this structural polymorphism of the HIV-1 leader RNA acts as a molecular switch in the viral replication cycle.
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In HIV-1, the packaging sequences adopt two alternative conformations: a translationally active long-distance interaction and a packageable branched multiple hairpin form where the DIS and Gag-binding sites are exposed.
“in the case of HIV-1, the packaging sequences adopt two alternative conformations: a translationally active long-distance interaction and a “packageable” branched multiple hairpin form where the DIS and Gag-binding sites are exposed”
From Beyond reverse transcription: molecular mechanisms and emerging paradigms in retroviral replication (2026) · cites this paper as Huthoff and Berkhout 2001
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Laughrea, M., & Jette, L. (1994) · Biochemistry · doi:10.1021/bi00249a035 · Cited by 237 · see citing works
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How retroviruses select their genomes
D'Souza, V., & Summers, M. F. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1210 · Cited by 339 · see citing works
Lever, A. M. L. (2007) · Advances in Pharmacology · doi:10.1016/s1054-3589(07)55001-5 · Cited by 103 · see citing works
Xing, L., Liang, C., & Kleiman, L. (2011) · Journal of Virology · doi:10.1128/jvi.02010-10 · Cited by 60 · see citing works
Beyond reverse transcription: molecular mechanisms and emerging paradigms in retroviral replication
Jehad, M. A., Ali, L. M., Pillai, V. N., Prabhu, S. G., Mustafa, F., & Rizvi, T. A. (2026) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaf066 · Cited by 5 · see citing works
“…sequences adopt two alternative conformations: a translationally active long-distance interaction and a “packageable” branched multiple hairpin form where the DIS and Gag-binding sites are exposed (Huthoff and Berkhout 2001 , Abbink and Berkhout 2003 , Abbink et al. 2005 , Keane et al. 2015 ).”
- Authors
- HUTHOFF, H., & BERKHOUT, B.
- Affiliations
- Amsterdam UMC Location University of Amsterdam (NL)
- Venue
- RNA
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2001-01
- Volume
- 7
- Issue
- 1
- Pages
- 143-157
- ISSN
- 1355-8382 (ISSN-L)
- PMC
- PMC1370064
- OpenAlex
- W1985665571
- Cited by
- 209
- References
- 1
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 3 · 2023: 3 · 2022: 11 · 2021: 9 · 2020: 7 · 2019: 9 · 2018: 3 · 2017: 5 · 2016: 8 · 2015: 6 · 2014: 10 · 2013: 6 · 2012: 11
- FWCI
- 4.78
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- RNA (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- RNA dimerization, viral life cycle, molecular switches
- MeSH terms
- Base Sequence, Hot Temperature, Humans, Models, Molecular, Molecular Sequence Data, Nucleic Acid Conformation, Nucleic Acid Denaturation, Poly A, Proviruses, RNA, Viral, Thermodynamics, HIV-1, Mutagenesis, Sequence Deletion, Alternative Splicing, Dimerization, RNA, Spliced Leader
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