Importance of Viral Late Domains in Budding and Release of Enveloped RNA Viruses DOI Creative Commons

Lisa Welker,

Jean‐Christophe Paillart, Serena Bernacchi

и другие.

Viruses, Год журнала: 2021, Номер 13(8), С. 1559 - 1559

Опубликована: Авг. 6, 2021

Late assembly (L) domains are conserved sequences that necessary for the late steps of viral replication, acting like cellular adaptors to engage ESCRT membrane fission machinery promote virion release. These short sequences, whose mutation or deletion produce accumulation immature virions at plasma membrane, were firstly identified within retroviral Gag precursors, and in a further step, also structural proteins many other enveloped RNA viruses including arenaviruses, filoviruses, rhabdoviruses, reoviruses, paramyxoviruses. Three classes L have been thus far (PT/SAP, YPXnL/LXXLF, PPxY), even if it has recently suggested motifs could act as domains. Here, we summarize current state knowledge different types their partners budding events viruses, with particular focus on retroviruses.

Язык: Английский

The Neuronal Gene Arc Encodes a Repurposed Retrotransposon Gag Protein that Mediates Intercellular RNA Transfer DOI Creative Commons

Elissa D. Pastuzyn,

Cameron E. Day,

Rachel B. Kearns

и другие.

Cell, Год журнала: 2018, Номер 172(1-2), С. 275 - 288.e18

Опубликована: Янв. 1, 2018

Язык: Английский

Процитировано

517

Transcriptional start site heterogeneity modulates the structure and function of the HIV-1 genome DOI Open Access
Siarhei Kharytonchyk,

Sarah Monti,

Philip J. Smaldino

и другие.

Proceedings of the National Academy of Sciences, Год журнала: 2016, Номер 113(47), С. 13378 - 13383

Опубликована: Ноя. 9, 2016

Significance Current dogma states that the integrated HIV type 1 provirus encodes a single RNA transcript serves as both mRNA for generating viral proteins and genomic is packaged used reverse transcription. We now show multiple transcripts with different functions are generated in infected cells, consequence of heterogeneous transcriptional start site usage. Transcripts begin capped guanosine specifically selected packaging, whereas those two or three guanosines enriched on polysomes translation. In vitro studies recombinant 5′-leader reveal mechanism by which incorporation 5′ dramatically alters structure, function, fate RNA.

Язык: Английский

Процитировано

97

Nano-DMS-MaP allows isoform-specific RNA structure determination DOI Creative Commons
Patrick Bohn, Anne-Sophie Gribling-Burrer, Uddhav B. Ambi

и другие.

Nature Methods, Год журнала: 2023, Номер 20(6), С. 849 - 859

Опубликована: Апрель 27, 2023

Abstract Genome-wide measurements of RNA structure can be obtained using reagents that react with unpaired bases, leading to adducts identified by mutational profiling on next-generation sequencing machines. One drawback these experiments is short reads rarely mapped specific transcript isoforms. Consequently, information acquired as a population average in regions are shared between transcripts, thus blurring the underlying structural landscape. Here, we present nanopore dimethylsulfate (Nano-DMS-MaP)—a method exploits long-read provide isoform-resolved highly similar molecules. We demonstrate value Nano-DMS-MaP resolving complex landscape human immunodeficiency virus-1 transcripts infected cells. show unspliced and spliced have distinct structures at packaging site within common 5′ untranslated region, likely explaining why viral RNAs excluded from particles. Thus, straightforward resolve biologically important transcript-specific were previously hidden short-read ensemble analyses.

Язык: Английский

Процитировано

25

Retroviral RNA Dimerization: From Structure to Functions DOI Creative Commons

Noé Dubois,

Roland Marquet, Jean‐Christophe Paillart

и другие.

Frontiers in Microbiology, Год журнала: 2018, Номер 9

Опубликована: Март 22, 2018

The genome of the retroviruses is a dimer composed by two homologous copies genomic RNA (gRNA) molecules positive polarity. dimerization process allows gRNA to be non-covalently linked together through intermolecular base-pairing. This step critical for viral life cycle and highly conserved among with exception spumaretroviruses. Furthermore, packaging into particles presents an important evolutionary advantage immune system evasion drug resistance. Recent studies reported switches models regulating not only dimerization, but also translation packaging, spatio-temporal characterization within cells are now at hand. review summarizes our current understanding on structural features signals variety (HIVs, MLV, RSV, BLV, MMTV, MPMV…), mechanisms formation functional implications in retroviral cycle.

Язык: Английский

Процитировано

72

Identification of the initial nucleocapsid recognition element in the HIV-1 RNA packaging signal DOI Creative Commons
Pengfei Ding, Siarhei Kharytonchyk, Alexis Waller

и другие.

Proceedings of the National Academy of Sciences, Год журнала: 2020, Номер 117(30), С. 17737 - 17746

Опубликована: Июль 9, 2020

Significance Understanding the molecular determinants of retroviral genome packaging is important for drug discovery and development vectors gene delivery. We show that HIV-1 leader, which contains RNA elements necessary packaging, binds approximately two dozen copies cognate NC protein with affinities ranging from ∼40 nM to 1.4 µM. Binding four highest-affinity “initial” binding sites occurs endothermic energetics attributed NC-induced localized melting. Mutations stabilize these inhibit in vitro transfected cells. A small-molecule inhibitor specifically initial stabilizes structure. Our findings identify a potential Achilles’ heel HIV therapeutic development.

Язык: Английский

Процитировано

66

Epitranscriptomic regulation of HIV-1 full-length RNA packaging DOI Creative Commons
Camila Pereira-Montecinos, Daniela Toro‐Ascuy,

Catarina Ananías-Sáez

и другие.

Nucleic Acids Research, Год журнала: 2022, Номер 50(4), С. 2302 - 2318

Опубликована: Янв. 26, 2022

During retroviral replication, the full-length RNA serves both as mRNA and genomic RNA. However, mechanisms by which HIV-1 Gag protein selects two molecules that will be packaged into nascent virions remain poorly understood. Here, we demonstrate deposition of N6-methyladenosine (m6A) regulates packaging. While m6A METTL3/METTL14 onto was associated with increased synthesis reduced packaging, FTO-mediated demethylation promoted incorporation viral particles. Interestingly, associates demethylase FTO in nucleus contributes to demethylation. We further identified highly conserved adenosines within 5'-UTR have a crucial functional role methylation packaging Together, our data propose novel epitranscriptomic mechanism allowing selection used genomes.

Язык: Английский

Процитировано

34

Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products DOI Creative Commons
Ramandeep Kaur, Pooja Sharma, Girish Kumar Gupta

и другие.

Molecules, Год журнала: 2020, Номер 25(9), С. 2070 - 2070

Опубликована: Апрель 29, 2020

Acquired Immunodeficiency Syndrome (AIDS), which chiefly originatesfroma retrovirus named Human Virus (HIV), has impacted about 70 million people worldwide. Even though several advances have been made in the field of antiretroviral combination therapy, HIV is still responsible for a considerable number deaths Africa. The current therapies achieved success providing instant suppression but with countless undesirable adverse effects. Presently, biodiversity plant kingdom being explored by researchers discovery potent anti-HIV drugs different mechanisms action. primary challenge to afford treatment that free from any sort risk drug resistance and serious side Hence, there strong demand evaluate derived plants as well their derivatives. Several plants, such Andrographis paniculata, Dioscorea bulbifera, Aegle marmelos, Wistaria floribunda, Lindera chunii, Xanthoceras sorbifolia others displayed significant activity. Here, weattempt summarize main results, focus on structures most plant-based natural products having activity along action IC50 values, structure-activity-relationships important key findings.

Язык: Английский

Процитировано

50

RNA Structure—A Neglected Puppet Master for the Evolution of Virus and Host Immunity DOI Creative Commons
Redmond P. Smyth, Matteo Negroni, Andrew Lever

и другие.

Frontiers in Immunology, Год журнала: 2018, Номер 9

Опубликована: Сен. 19, 2018

The central dogma of molecular biology describes the flow genetic information from DNA to protein via an RNA intermediate. For many years, has been considered simply as a messenger relaying between and proteins. Recent advances in next generation sequencing technology, bioinformatics non-coding have highlighted important roles virtually every biological process. Our understanding further enriched by number significant probing structures. It is now appreciated that cellular viral processes are highly dependent on specific structures / or sequences, such reliance will undoubtedly impact evolution both hosts viruses. As contribution this special issue host immunity virus evolution, it timely consider how sequences could directly influence co-evolution In manuscript, we begin stating some basic principles structures, followed describing critical viruses hosts. More importantly, highlight available new tools predict evaluate novel pointing out limitations readers should be aware their own analyses.

Язык: Английский

Процитировано

48

5′-Cap sequestration is an essential determinant of HIV-1 genome packaging DOI Creative Commons
Pengfei Ding, Siarhei Kharytonchyk,

Nansen Kuo

и другие.

Proceedings of the National Academy of Sciences, Год журнала: 2021, Номер 118(37)

Опубликована: Сен. 7, 2021

Significance HIV-1 replication is critically dependent on the selective incorporation of viral RNA genomes into assembling virions. Although elements that promote packaging have been identified, determinants authentic fidelity and efficiency until now remained unknown. The present studies show genome selection achieved by a bipartite mechanism requires both dimerization-dependent exposure signals within 5′ leader structural sequestration cap. Cap likely prevents capture cellular processing translation machinery, may help explain why some polymerase III transcripts lack caps can parasitize be commonly employed among viruses package 5′-capped genomes.

Язык: Английский

Процитировано

41

Short- and long-range interactions in the HIV-1 5′ UTR regulate genome dimerization and packaging DOI Creative Commons
Liqing Ye, Anne-Sophie Gribling-Burrer, Patrick Bohn

и другие.

Nature Structural & Molecular Biology, Год журнала: 2022, Номер 29(4), С. 306 - 319

Опубликована: Март 28, 2022

Abstract RNA dimerization is the noncovalent association of two human immunodeficiency virus-1 (HIV-1) genomes. It a conserved step in HIV-1 life cycle and assumed to be prerequisite for binding viral structural protein Pr55 Gag during genome packaging. Here, we developed functional analysis structure-sequencing (FARS-seq) comprehensively identify sequences structures within 5′ untranslated region (UTR) that regulate this critical step. Using FARS-seq, found nucleotides important throughout UTR identified distinct conformations monomeric dimeric RNA. In RNA, key domains, such as stem-loop 1 (SL1), polyadenylation signal (polyA) primer site (PBS), folded into independent motifs. SL1 was reconfigured long- short-range base pairings with polyA PBS, respectively. We show these interactions disrupt packaging, additionally PBS–SL1 interaction unexpectedly couples PBS binding. Altogether, our data provide insights late stages mechanistic explanation link between

Язык: Английский

Процитировано

29