Evidence map›Paper›PMID 23907385›Full record

ArticleNucleic acids research2013

A multidimensional platform for the purification of non-coding RNA species.

Yok Hian Chionh, Chia-Hua Ho, Dumnoensun Pruksakorn, I Ramesh Babu, Chee Sheng Ng, Fabian Hia, Megan E McBee, Dan Su, Yan Ling Joy Pang, Chen Gu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  5. Strategies to Avoid Artifacts in Mass Spectrometry-Based Epitranscriptome Analyses.Angewandte Chemie (International ed. in English) · 2021
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  9. The rRNA mGenes & development · 2020
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  14. Review
  15. Article
  16. NAIL-MS in E. coli Determines the Source and Fate of Methylation in tRNA.Chembiochem : a European journal of chemical biology · 2018
    Article
  17. Article
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  19. Three distinct 3-methylcytidine (mThe Journal of biological chemistry · 2017
    Article
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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

16 authors at 5 institutions in 4 countries.

Yok Hian ChionhSingapore-MIT Alliance for Research and Technology, Infectious Disease Interdisciplinary Research Group, Campus for Research Excellence and Technological Enterprise, Singapore 138602, Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Department of Biological Engineering and Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA, Applied Biological Science Program, Chulabhorn Graduate Institute, Bangkok 10210, Thailand, Division of Molecular Genetics & Cell Biology, School of Biological Sciences, Nanyang Technological University, Singapore 637551, Immunology Programme, Life Science Institute, Centre for Life Science, Singapore 117456 and Novartis Institute for Tropical Disease, Singapore 138670.
Chia-Hua Ho
Dumnoensun Pruksakorn
I Ramesh Babu
Chee Sheng Ng
Fabian Hia
Megan E McBee
Dan Su
Yan Ling Joy Pang
Chen Gu
Hongping Dong
Erin G Prestwich
Pei-Yong Shi
Peter Rainer Preiser
Sylvie Alonso
Peter C Dedon
Massachusetts Institute of Technology · USSingapore-MIT Alliance for Research and Technology · SGNovartis (China) · CNCenter for Environmental Health · USNanyang Technological University · SG

Funding

TOXICOLOGY CORE UNITP30ES002109 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LEVINE, STUART S · 1985 to 2020
$25.6M
RNA Modifications as Biomarkers of Environmental Stress and InflammationR01ES017010 · NIEHS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI BEGLEY, THOMAS J · 2009 to 2013
$2.1M
NIEHS NIH HHS ES002109NIEHS NIH HHS ES017010NIEHS NIH HHS P30 ES002109
6 · The paper itself

Abstract

A renewed interest in non-coding RNA (ncRNA) has led to the discovery of novel RNA species and post-transcriptional ribonucleoside modifications, and an emerging appreciation for the role of ncRNA in RNA epigenetics. Although much can be learned by amplification-based analysis of ncRNA sequence and quantity, there is a significant need for direct analysis of RNA, which has led to numerous methods for purification of specific ncRNA molecules. However, no single method allows purification of the full range of cellular ncRNA species. To this end, we developed a multidimensional chromatographic platform to resolve, isolate and quantify all canonical ncRNAs in a single sample of cells or tissue, as well as novel ncRNA species. The applicability of the platform is demonstrated in analyses of ncRNA from bacteria, human cells and plasmodium-infected reticulocytes, as well as a viral RNA genome. Among the many potential applications of this platform are a system-level analysis of the dozens of modified ribonucleosides in ncRNA, characterization of novel long ncRNA species, enhanced detection of rare transcript variants and analysis of viral genomes.

Indexed as

Chromatography, GelChromatography, High Pressure LiquidChromatography, Reverse-PhaseFluorometryHumansMicroRNAsMycobacterium bovisPlasmodium bergheiRNA, BacterialRNA, ProtozoanRNA, RibosomalRNA, TransferRNA, UntranslatedRNA, ViralMicroRNAsRNA, BacterialRNA, ProtozoanRNA, RibosomalRNA, TransferRNA, UntranslatedRNA, Viral

Identifiers

PMID23907385
PMCPMC3783195
OpenAlexW2162859338

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.