Evidence map›Paper›PMID 19535461›Full record

ArticleRNA (New York, N.Y.)2009

SHAMS: combining chemical modification of RNA with mass spectrometry to examine polypurine tract-containing RNA/DNA hybrids.

Kevin B Turner, Hye Young Yi-Brunozzi, Robert G Brinson, John P Marino, Daniele Fabris, Stuart F J Le Grice

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Structure-specific ribonucleases for MS-based elucidation of higher-order RNA structure.Journal of the American Society for Mass Spectrometry · 2014
    Article
  5. Article
  6. Article
  7. The mechanisms of RNA SHAPE chemistry.Journal of the American Chemical Society · 2012
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Infrared multiphoton dissociation of small-interfering RNA anions and cations.Journal of the American Society for Mass Spectrometry · 2010
    Article
  16. Article
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

6 authors at 3 institutions in 1 country.

Kevin B TurnerDepartment of Chemistry and Biochemistry, University of Maryland Baltimore County, Baltimore, Maryland 21250, USA.
Hye Young Yi-Brunozzi
Robert G Brinson
John P Marino
Daniele Fabris
Stuart F J Le Grice
National Institutes of Health · USUniversity of Maryland, Baltimore County · USBiotechnology Institute · US

Funding

Nucleic Acid Footprinting and development of small molecule antagonistsZIABC010493 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LE GRICE, STUART F. J. · 2009 to 2021
$9.3M
STRUCTURAL BASIS OF RNA STEM LOOP KISSING INTERACTIONSR01GM059107 · NIGMS · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI MARINO, JOHN PAUL · 1999 to 2008
$1.7M
Intramural NIH HHSNIGMS NIH HHS GM59107NIGMS NIH HHS GM643208NIGMS NIH HHS R01 GM059107
6 · The paper itself

Abstract

Selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) has gained popularity as a facile method of examining RNA structure both in vitro and in vivo, exploiting accessibility of the ribose 2'-OH to acylation by N-methylisatoic anhydride (NMIA) in unpaired or flexible configurations. Subsequent primer extension terminates at the site of chemical modification, and these products are fractionated by high-resolution gel electrophoresis. When applying SHAPE to investigate structural features associated with the wild-type and analog-substituted polypurine tract (PPT)-containing RNA/DNA hybrids, their size (20-25 base pairs) rendered primer extension impractical. As an alternative method of detection, we reasoned that chemical modification could be combined with tandem mass spectrometry, relying on the mass increment of RNA fragments containing the NMIA adduct (M(r) = 133 Da). Using this approach, we demonstrate both specific modification of the HIV-1 PPT RNA primer and variations in its acylation pattern induced by replacing template nucleotides with a non-hydrogen-bonding thymine isostere. Our selective 2'-hydroxyl acylation analyzed by mass spectrometry strategy (SHAMS) should find utility when examining the structure of small RNA fragments or RNA/DNA hybrids where primer extension cannot be performed.

Indexed as

AcylationBase SequenceDNADNA, FungalDNA, ViralHIV-1Nuclear Magnetic Resonance, BiomolecularNucleic Acid HeteroduplexesNucleic Acid HybridizationRNARNA-Directed DNA PolymeraseRNA, FungalRNA, ViralSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTandem Mass SpectrometryDNADNA, FungalDNA, ViralNucleic Acid Heteroduplexesreverse transcriptase Ty3, S cerevisiaeRNARNA-Directed DNA PolymeraseRNA, FungalRNA primersRNA, ViralSaccharomyces cerevisiae Proteins

Identifiers

PMID19535461
PMCPMC2714758
OpenAlexW2171461613

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.