Evidence map›Paper›PMID 24999558›Full record

ArticleJournal of proteome research2014

Discovery of Chromatin-Associated Proteins via Sequence-Specific Capture and Mass Spectrometric Protein Identification in Saccharomyces cerevisiae.

Julia Kennedy-Darling, Hector Guillen-Ahlers, Michael R Shortreed, Mark Scalf, Brian L Frey, Christina Kendziorski, Michael Olivier, Audrey P Gasch, Lloyd M Smith

Abstract read
In one paragraph

Article in Journal of proteome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Proximity Labeling in Plants.Annual review of plant biology · 2023
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
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  12. Article
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  15. Review
  16. Multiplexed programmable release of captured DNA.Chembiochem : a European journal of chemical biology · 2014
    Article
  17. 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

9 authors.

Julia Kennedy-Darling
Hector Guillen-Ahlers‡Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas 78227, United States.
Michael R Shortreed
Mark Scalf
Brian L Frey
Christina Kendziorski
Michael Olivier‡Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas 78227, United States.
Audrey P Gasch
Lloyd M Smith

Funding

Institutional Training in the Genomic SciencesT32HG002760 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI Qiongshi Lu · 2003 to 2026
$17.7M
Wisconsin Center of Excellence in Genomics ScienceP50HG004952 · NHGRI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI OLIVIER, MICHAEL · 2009 to 2013
$13.0M
NHGRI NIH HHS 1P50 HG004952NHGRI NIH HHS P50 HG004952NHGRI NIH HHS T32 HG002760
6 · The paper itself

Abstract

DNA-protein interactions play critical roles in the control of genome expression and other fundamental processes. An essential element in understanding how these systems function is to identify their molecular components. We present here a novel strategy, Hybridization Capture of Chromatin Associated Proteins for Proteomics (HyCCAPP), to identify proteins that are interacting with any given region of the genome. This technology identifies and quantifies the proteins that are specifically interacting with a genomic region of interest by sequence-specific hybridization capture of the target region from in vivo cross-linked chromatin, followed by mass spectrometric identification and quantification of associated proteins. We demonstrate the utility of HyCCAPP by identifying proteins associated with three multicopy and one single-copy loci in yeast. In each case, a locus-specific pattern of target-associated proteins was revealed. The binding of previously unknown proteins was confirmed by ChIP in 11 of 17 cases. The identification of many previously known proteins at each locus provides strong support for the ability of HyCCAPP to correctly identify DNA-associated proteins in a sequence-specific manner, while the discovery of previously unknown proteins provides new biological insights into transcriptional and regulatory processes at the target locus.

Indexed as

Mass SpectrometryChromatinChromatin ImmunoprecipitationComputational BiologyDNADNA-Binding ProteinsNucleic Acid HybridizationPolymerase Chain ReactionPromoter Regions, GeneticProtein BindingProtein Interaction MappingProteomeProteomicsRibosomesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsChromatinDNADNA-Binding ProteinsProteomeSaccharomyces cerevisiae ProteinsTranscription FactorsChIPchromatinchromatin immunoprecipitationDNA-binding proteinsDNA−protein interactionsGENECAPPhybridizationHyCCAPPmass spectrometryproteomicsrDNAribosome biogenesistranscriptional regulationtranscription factorsX-element

Identifiers

PMID24999558
PMCPMC4123949

What OpenQuestion holds

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Registered trials

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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.