Evidence map›Paper›PMID 42862222›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2027

Key Points to Consider When Studying RNA Remodeling by Proteins.

William Luke Ward, Rick Russell

Abstract readReview
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In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

William Luke WardDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX, 78712, USA.
Rick RussellDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX, 78712, USA. rick_russell@cm.utexas.edu.ORCID http://orcid.org/0000-0002-4879-8563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular RNAs depend on proteins for efficient folding to specific functional structures and for transitions between functional structures. This dependence arises from intrinsic properties of RNA structure. Specifically, RNAs possess stable local structure, largely in the form of helices, and there are abundant opportunities for RNAs to form alternative helices and tertiary contacts and therefore to populate alternative structures. Proteins with RNA chaperone activity, either ATP-dependent or ATP-independent, can promote structural transitions by interacting with single-stranded RNA (ssRNA) to compete away partner interactions and then release ssRNA so that it can form new interactions. In this chapter, we review the basic properties of RNA and the proteins that function as chaperones and remodelers. We then use these properties as a foundation to explore key points for the design and interpretation of experiments that probe RNA rearrangements and their acceleration by proteins.

Indexed as

RNARNA-Binding ProteinsAdenosine TriphosphateHumansMolecular ChaperonesNucleic Acid ConformationRNA FoldingAdenosine TriphosphateMolecular ChaperonesRNARNA-Binding ProteinsADP-BeF3AMP-PNPATP analogsHelicasesRNA foldingRNA remodeling

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.