Evidence map›Paper›PMID 26646615›Full record

ArticlePLoS genetics2015

Probing Xist RNA Structure in Cells Using Targeted Structure-Seq.

Rui Fang, Walter N Moss, Michael Rutenberg-Schoenberg, Matthew D Simon

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 130 citations in OpenAlex.

  1. Review
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  13. Estimating RNA Secondary Structure Folding Free Energy Changes with efn2.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Article
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  19. Article
  20. Targeting RNA structures with small molecules.Nature reviews. Drug discovery · 2022
    Review

21 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Rui FangDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, Connecticut, United States of America.
Walter N MossDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, Connecticut, United States of America.
Michael Rutenberg-SchoenbergDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, Connecticut, United States of America.
Matthew D SimonDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, Connecticut, United States of America.
Yale University · US

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
VIRAL SMALL RNPS--ROLES IN CELL TRANSFORMATIONP01CA016038 · NCI · YALE UNIVERSITY · PI DIMAIO, DANIEL C. · 1985 to 2020
$25.6M
Integrating RNAs into signaling pathways by engineering covalent RNA modificationDP2HD083992 · NICHD · YALE UNIVERSITY · PI SIMON, MATTHEW DAVID · 2014 to 2014
$2.5M
Understanding Epstein Barr virus oncogenicity through non-coding RNA structureK99GM112877 · NIGMS · YALE UNIVERSITY · PI MOSS, WALTER · 2015 to 2015
$90k
NCCDPHP CDC HHS 1DP2HD083992NCI NIH HHS P01 CA016038NICHD NIH HHS DP2 HD083992NIGMS NIH HHS 1K99GM112877-01NIGMS NIH HHS K99 GM112877NIGMS NIH HHS T32 GM007223
6 · The paper itself

Abstract

The long non-coding RNA (lncRNA) Xist is a master regulator of X-chromosome inactivation in mammalian cells. Models for how Xist and other lncRNAs function depend on thermodynamically stable secondary and higher-order structures that RNAs can form in the context of a cell. Probing accessible RNA bases can provide data to build models of RNA conformation that provide insight into RNA function, molecular evolution, and modularity. To study the structure of Xist in cells, we built upon recent advances in RNA secondary structure mapping and modeling to develop Targeted Structure-Seq, which combines chemical probing of RNA structure in cells with target-specific massively parallel sequencing. By enriching for signals from the RNA of interest, Targeted Structure-Seq achieves high coverage of the target RNA with relatively few sequencing reads, thus providing a targeted and scalable approach to analyze RNA conformation in cells. We use this approach to probe the full-length Xist lncRNA to develop new models for functional elements within Xist, including the repeat A element in the 5'-end of Xist. This analysis also identified new structural elements in Xist that are evolutionarily conserved, including a new element proximal to the C repeats that is important for Xist function.

Indexed as

Evolution, MolecularNucleic Acid ConformationAnimalsDNA MethylationHumansMicePoint MutationRNA FoldingRNA, Long NoncodingRNA, RibosomalSequence AlignmentSequence Analysis, RNAX ChromosomeX Chromosome InactivationRNA, Long NoncodingRNA, RibosomalXIST non-coding RNA

Identifiers

PMID26646615
PMCPMC4672913
OpenAlexW2194615260

What OpenQuestion holds

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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 OpenQuestion graph.