Evidence map›Paper›PMID 36635406›Full record

ReviewNature reviews. Genetics2023

High-throughput biochemistry in RNA sequence space: predicting structure and function.

Emil Marklund, Yuxi Ke, William J Greenleaf

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Structure-Based Prediction of lncRNA-Protein Interactions by Deep Learning.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Article
  11. Review
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

3 authors at 1 institution in 1 country.

Emil MarklundDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-1150-7304
Yuxi KeDepartment of Bioengineering, Stanford University, Stanford, CA, USA.ORCID 0000-0003-1131-0998
William J GreenleafDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA. wjg@stanford.edu.ORCID 0000-0003-1409-3095
Stanford University · US

Funding

Time-resolved small angle X-ray scatteringP01GM066275 · NIGMS · STANFORD UNIVERSITY · PI HERSCHLAG, DANIEL · 2003 to 2017
$17.8M
Special EquipmentP50HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2014 to 2018
$15.2M
Genome wide identification and functional analysis of chromatin regulatory RNAsR01HG009909 · NHGRI · STANFORD UNIVERSITY · PI GREENLEAF, WILLIAM JAMES, STRAIGHT, AARON F · 2018 to 2021
$2.5M
Quantitative high-throughput nucleic acid assays on a sequencing chipR01GM111990 · NIGMS · STANFORD UNIVERSITY · PI GREENLEAF, WILLIAM JAMES · 2014 to 2018
$1.5M
NHGRI NIH HHS P50 HG007735NHGRI NIH HHS R01 HG009909NIGMS NIH HHS P01 GM066275NIGMS NIH HHS R01 GM111990
6 · The paper itself

Abstract

RNAs are central to fundamental biological processes in all known organisms. The set of possible intramolecular interactions of RNA nucleotides defines the range of alternative structural conformations of a specific RNA that can coexist, and these structures enable functional catalytic properties of RNAs and/or their productive intermolecular interactions with other RNAs or proteins. However, the immense combinatorial space of potential RNA sequences has precluded predictive mapping between RNA sequence and molecular structure and function. Recent advances in high-throughput approaches in vitro have enabled quantitative thermodynamic and kinetic measurements of RNA-RNA and RNA-protein interactions, across hundreds of thousands of sequence variations. In this Review, we explore these techniques, how they can be used to understand RNA function and how they might form the foundations of an accurate model to predict the structure and function of an RNA directly from its nucleotide sequence. The experimental techniques and modelling frameworks discussed here are also highly relevant for the sampling of sequence-structure-function space of DNAs and proteins.

Indexed as

DNARNABase SequenceNucleic Acid ConformationSequence Analysis, RNADNARNA

Identifiers

PMID36635406
OpenAlexW4315786298

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.