Evidence map›Paper›PMID 20123731›Full record

ArticleNucleic acids research2010

Translational control analysis by translationally active RNA capture/microarray analysis (TrIP-Chip).

Kenji Kudo, Yaguang Xi, Yuan Wang, Bo Song, Edward Chu, Jingyue Ju, James J Russo, Jingfang Ju

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2010. 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
1.1field-weighted citation impact, top 23% 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, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Activation of EIF4E by Aurora Kinase A Depicts a Novel Druggable Axis in Everolimus-Resistant Cancer Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Toward a genome-wide landscape of translational control.Cold Spring Harbor perspectives in biology · 2013
    Review
  12. Article
  13. Translational regulation in nutrigenomics.Advances in nutrition (Bethesda, Md.) · 2011
    Review
  14. Article
  15. Article
  16. Review
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

8 authors at 1 institution in 1 country.

Kenji KudoMitchell Cancer Institute, Mobile, AL 36688, USA.
Yaguang Xi
Yuan Wang
Bo Song
Edward Chu
Jingyue Ju
James J Russo
Jingfang Ju
USA Mitchell Cancer Institute · US

Funding

Modulation of Serotonergic TransportersR01MH075020 · NIMH · GEORGETOWN UNIVERSITY · PI SIDHU, ANITA · 2007 to 2010
$1.3M
Novel Method for Isolating Actively Translated mRNAsR21CA114043 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI JU, JINGFANG · 2006 to 2007
$259k
NCI NIH HHS CA114043NCI NIH HHS R21 CA114043NIMH NIH HHS MH075020
6 · The paper itself

Abstract

We have developed a new approach to systematically study post-transcriptional regulation in a small number of cells. Actively translating mRNAs are associated with polysomes and the newly synthesized peptide chains are closely associated with molecular chaperones such as hsp70s, which assist in the proper folding of nascent polypeptides into higher ordered structures. These chaperones provide an anchor with which to separate actively translating mRNAs associated with polysomes from free mRNAs. Affinity capture beads were developed to capture hsp70 chaperones associated with the polysome complexes. The isolated actively translating mRNAs were used for high-throughput expression profiling analysis. Feasibility was demonstrated using an in vitro translation system with known translationally regulated mRNA transcript thymidylate synthase (TS). We further developed the approach using HCT-116 colon cancer cells with both TS and p53 as positive controls. The steady-state levels of TS and p53 mRNAs were unaltered after 5-fluorouracil treatment as assessed by real-time qRT-PCR analysis. In contrast, the protein expression and polysome-associated mRNA levels of both genes were increased. These differences in translational rate were revealed with our new approach from 500 cells. This technology has the potential to make investigation of translational control feasible with limited quantities of clinical specimens.

Indexed as

Gene Expression RegulationProtein BiosynthesisAntibodiesAntimetabolites, AntineoplasticCell Line, TumorFluorouracilGene Expression ProfilingHSP70 Heat-Shock ProteinsHumansImmunoprecipitationOligonucleotide Array Sequence AnalysisPolyribosomesRNA, MessengerAntibodiesAntimetabolites, AntineoplasticFluorouracilHSP70 Heat-Shock ProteinsRNA, Messenger

Identifiers

PMID20123731
PMCPMC2875024
OpenAlexW2160257303

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.