Evidence map›Paper›PMID 24997788›Full record

ArticleNature biotechnology2014

Revealing long noncoding RNA architecture and functions using domain-specific chromatin isolation by RNA purification.

Jeffrey J Quinn, Ibrahim A Ilik, Kun Qu, Plamen Georgiev, Ci Chu, Asifa Akhtar, Howard Y Chang

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
8.7field-weighted citation impact, top 1% 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

100 citing papers in PubMed, 182 citations in OpenAlex.

  1. Review
  2. Article
  3. Microfluidic low-input profiling reveals lncRNA roles in disease.bioRxiv : the preprint server for biology · 2026
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  5. Review
  6. Review
  7. Review
  8. From the genome's perspective: Bearing somatic retrotransposition to leverage the regulatory potential of L1 RNAs.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  9. Article
  10. N-terminus ofeLife · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. RNA-Chrom: a manually curated analytical database of RNA-chromatin interactome.Database : the journal of biological databases and curation · 2023
    Article
  15. Review
  16. Review
  17. Review
  18. Methods to Study RNA-Chromatin Interactions.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  19. Small molecule quercetin bindsMolecular therapy. Nucleic acids · 2022
    Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Jeffrey J QuinnHoward Hughes Medical Institute and Program in Epithelial Biology, Stanford University School of Medicine, Stanford CA 94305, USA.
Ibrahim A Ilik *Max Planck Institute of Immunobiology and Epigenetics, Stübeweg 51, 79108 Freiburg im Breisgau, Germany.
Kun Qu *Howard Hughes Medical Institute and Program in Epithelial Biology, Stanford University School of Medicine, Stanford CA 94305, USA.
Plamen Georgiev *Max Planck Institute of Immunobiology and Epigenetics, Stübeweg 51, 79108 Freiburg im Breisgau, Germany.
Ci ChuHoward Hughes Medical Institute and Program in Epithelial Biology, Stanford University School of Medicine, Stanford CA 94305, USA.
Asifa AkhtarMax Planck Institute of Immunobiology and Epigenetics, Stübeweg 51, 79108 Freiburg im Breisgau, Germany.
Howard Y ChangHoward Hughes Medical Institute and Program in Epithelial Biology, Stanford University School of Medicine, Stanford CA 94305, USA.
Max Planck Institute of Immunobiology and Epigenetics · DEHoward Hughes Medical Institute · USStanford University · US

Funding

Wound Response Genes in Cancer ProgressionR01CA118750 · NCI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2007 to 2016
$2.9M
LncRNA regulation of environmental responseR01ES023168 · NIEHS · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2013 to 2016
$2.2M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA118750NCI NIH HHS R01-CA118750NIEHS NIH HHS R01 ES023168NIEHS NIH HHS R01-ES023168
6 · The paper itself

Abstract

Little is known about the functional domain architecture of long noncoding RNAs (lncRNAs) because of a relative paucity of suitable methods to analyze RNA function at a domain level. Here we describe domain-specific chromatin isolation by RNA purification (dChIRP), a scalable technique to dissect pairwise RNA-RNA, RNA-protein and RNA-chromatin interactions at the level of individual RNA domains in living cells. dChIRP of roX1, a lncRNA essential for Drosophila melanogaster X-chromosome dosage compensation, reveals a 'three-fingered hand' ribonucleoprotein topology. Each RNA finger binds chromatin and the male-specific lethal (MSL) protein complex and can individually rescue male lethality in roX-null flies, thus defining a minimal RNA domain for chromosome-wide dosage compensation. dChIRP improves the RNA genomic localization signal by >20-fold relative to previous techniques, and these binding sites are correlated with chromosome conformation data, indicating that most roX-bound loci cluster in a nuclear territory. These results suggest dChIRP can reveal lncRNA architecture and function with high precision and sensitivity.

Indexed as

AnimalsBinding SitesChromatinDosage Compensation, GeneticFemaleMaleRNARNA, Long NoncodingChromatinRNARNA, Long Noncoding

Identifiers

PMID24997788
PMCPMC4175979
OpenAlexW2074975948

What OpenQuestion holds

Textmetadata
LicenceTDM
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.