Evidence map›Paper›PMID 10557283›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Identification of eukaryotic mRNAs that are translated at reduced cap binding complex eIF4F concentrations using a cDNA microarray.

G Johannes, M S Carter, M B Eisen, P O Brown, P Sarnow

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 176 papers.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed
14.3field-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

176 citing papers in PubMed, 387 citations in OpenAlex.

  1. Article
  2. Microarrays and the Dawn of Omics Data Analysis.Advances in experimental medicine and biology · 2026
    Review
  3. Fluorescence-Based mRNA Translation Reporter.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Analysis of mRNA Translation by Polysome Profiling.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. RNA sequencing: the teenage years.Nature reviews. Genetics · 2019
    Review

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

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

5 authors at 2 institutions in 1 country.

G JohannesDepartment of Microbiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
M S Carter
M B Eisen
P O Brown
P Sarnow
Stanford University · USHoward Hughes Medical Institute · US

Funding

TRANSLATIONAL INITIATION IN EUKARYOTIC MRNA MOLECULESR01GM055979 · NIGMS · STANFORD UNIVERSITY · PI SARNOW, PETER · 1996 to 2005
$1.2M
ANTENNAPEDIA MRNA PROTEIN INTERACTIONSF32GM016751 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI JOHANNES, GREGG J · 1995 to 1996
–
NIGMS NIH HHS F32 GM016751NIGMS NIH HHS F32 GM16751NIGMS NIH HHS R01 GM055979NIGMS NIH HHS R01 GM55979
6 · The paper itself

Abstract

Although most eukaryotic mRNAs need a functional cap binding complex eIF4F for efficient 5' end- dependent scanning to initiate translation, picornaviral, hepatitis C viral, and a few cellular RNAs have been shown to be translated by internal ribosome entry, a mechanism that can operate in the presence of low levels of functional eIF4F. To identify cellular mRNAs that can be translated when eIF4F is depleted or in low abundance and that, therefore, may contain internal ribosome entry sites, mRNAs that remained associated with polysomes were isolated from human cells after infection with poliovirus and were identified by using a cDNA microarray. Approximately 200 of the 7000 mRNAs analyzed remained associated with polysomes under these conditions. Among the gene products encoded by these polysome-associated mRNAs were immediate-early transcription factors, kinases, and phosphatases of the mitogen-activated protein kinase pathways and several protooncogenes, including c-myc and Pim-1. In addition, the mRNA encoding Cyr61, a secreted factor that can promote angiogenesis and tumor growth, was selectively mobilized into polysomes when eIF4F concentrations were reduced, although its overall abundance changed only slightly. Subsequent tests confirmed the presence of internal ribosome entry sites in the 5' noncoding regions of both Cyr61 and Pim-1 mRNAs. Overall, this study suggests that diverse mRNAs whose gene products have been implicated in a variety of stress responses, including inflammation, angiogenesis, and the response to serum, can use translational initiation mechanisms that require little or no intact cap binding protein complex eIF4F.

Indexed as

Intercellular Signaling Peptides and ProteinsProtein BiosynthesisProtein Serine-Threonine KinasesCysteine-Rich Protein 61DNA, ComplementaryGrowth SubstancesHeLa CellsHumansImmediate-Early ProteinsNucleic Acid HybridizationPoliovirusProto-Oncogene ProteinsProto-Oncogene Proteins c-pim-1RNA CapsRNA, MessengerCCN1 protein, humanCysteine-Rich Protein 61DNA, ComplementaryGrowth SubstancesImmediate-Early ProteinsIntercellular Signaling Peptides and ProteinsPIM1 protein, humanProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-pim-1RNA CapsRNA, Messenger

Identifiers

PMID10557283
PMCPMC23910
OpenAlexW2021263359

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.