Evidence map›Paper›PMID 40521663›Full record

ArticleNucleic acids research2025

Conserved long-range interactions are required for stable folding of orthoflaviviral genomic RNA.

Michael Z Palo, Betty Ha, Christopher P Lapointe, Carlos Alvarado, John Janetzko, Jan E Carette, Joseph D Puglisi, Elisabetta Viani Puglisi

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Remodeling of mRNA by eIF4F in human translation initiation.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Michael Z PaloDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.ORCID 0000-0003-4883-6766
Betty HaDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.
Christopher P LapointeDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.
Carlos AlvaradoDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.
John JanetzkoDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94305, United States.
Jan E CaretteDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, United States.
Joseph D PuglisiDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.ORCID 0000-0001-9268-5112
Elisabetta Viani PuglisiDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.

Funding

CHEETAH Center for the Structural Biology of HIV Infection, Restriction, and Viral DynamicsU54AI170856 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI JOSEPH D PUGLISI · 2022 to 2026
$34.4M
Dynamics of TranslationR35GM145306 · NIGMS · STANFORD UNIVERSITY · PI JOSEPH D PUGLISI · 2022 to 2026
$3.8M
Blavatnik Family FoundationDamon Runyon Cancer Research Foundation DRG-2318-18NIAID NIH HHS U54 AI170856NIGMS NIH HHS R35 GM145306NIH HHS AI150464NIH HHS GM145306NIH HHS GM147609
6 · The paper itself

Abstract

Long-range tertiary interactions are a widespread structural feature in viral RNAs (vRNAs) and mRNAs. In the orthoflaviviruses, conserved complementary sequences in the 5' and 3' terminal regions have an essential role in viral replication. Long-range pairing of these conserved sequences is proposed to facilitate a switch between two alternative vRNA conformations. Yet the detailed nature of these interactions, their relative populations and their exchange are required to formulate a mechanistic model of their role in regulation of the viral life cycle. Here, we used single-molecule Förster resonance energy transfer to study the global conformation of vRNAs by measuring their end-to-end distances. We observed that vRNA conformation is heterogeneous, and that conformers with close end-to-end distances have unusual kinetic stability when compared with mRNA lacking these specific long-range interactions. vRNAs also partition between at least two stable states with a large rearrangement of the terminal regions (>50 Å change in end-to-end distance). We demonstrate that this bistability depends on long-range interactions and is modulated by host factors such as the initiation factor complex eIF4F. Understanding how vRNA and its stability is influenced by interactions with other host and viral factors will help to elucidate a mechanistic role for these highly conserved orthoflaviviral sequences.

Indexed as

RNA FoldingRNA, ViralFluorescence Resonance Energy TransferGenome, ViralNucleic Acid ConformationRNA, MessengerRNA StabilityRNA, MessengerRNA, Viral

Identifiers

PMID40521663
PMCPMC12168079

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.