Evidence map›Paper›PMID 15210968›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

Biochemical and functional analysis of a 9-nt RNA sequence that affects translation efficiency in eukaryotic cells.

Stephen A Chappell, Gerald M Edelman, Vincent P Mauro

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  4. Article
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  9. A researcher's guide to the galaxy of IRESs.Cellular and molecular life sciences : CMLS · 2017
    Review
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  11. 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

3 authors at 1 institution in 1 country.

Stephen A ChappellDepartment of Neurobiology, The Scripps Research Institute, and The Skaggs Institute for Chemical Biology, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Gerald M Edelman
Vincent P Mauro
Scripps Research Institute · US

Funding

CELL-CELL ADHESION AMONG EMBRYONIC CELLSR01HD009635 · NICHD · SCRIPPS RESEARCH INSTITUTE, THE · PI EDELMAN, GERALD · 1985 to 2006
$2.6M
Internal Initiation in the Translation of Cellular mRNAsR01GM061725 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI MAURO, VINCENT P · 2001 to 2004
$1.2M
CELL-CELL ADHESION AMONG EMBRYONIC CELLSR37HD009635 · NICHD · SCRIPPS RESEARCH INSTITUTE · PI EDELMAN, GERALD · 1986 to 1996
–
NICHD NIH HHS HD09635NICHD NIH HHS R01 HD009635NIGMS NIH HHS GM61725NIGMS NIH HHS R01 GM061725
6 · The paper itself

Abstract

We previously identified an internal ribosome entry site (IRES) within the 5' leader of the mRNA encoding the Gtx homeodomain protein and showed that shorter nonoverlapping segments of this 5' leader could enhance the translation of a second cistron in a dicistronic mRNA. One of these segments was 9 nt in length, and when multiple copies of this IRES module were linked together, IRES activity was greatly enhanced. To further expand the potential uses of these synthetic constructs and facilitate analyses of the mechanism by which they affect translation, we show here that an IRES containing five linked copies of the 9-nt sequence can also enhance translation in the 5' leader of a monocistronic mRNA. Moreover, a search for interactions of the IRES module with cellular factors revealed specific binding to 40S ribosomal subunits but not to other cellular components. Based on the results of earlier studies suggesting that this sequence could bind to a complementary segment of 18S rRNA, we tested various sequences for possible links between the length of the complementary match, their binding to ribosomes, and their influence on translational efficiency. We found that the length of the complementary match was directly correlated with the ability of RNA probes to bind to ribosomes. In addition, translation was maximally enhanced ( approximately 8-fold) by a 7-nt segment of the 9-nt element; the enhancement declined progressively as the complementary stretches became progressively longer or shorter. The results suggest that the Gtx 9-nt sequence affects translation efficiency by a mechanism that involves base pairing to 18S rRNA.

Indexed as

5' Untranslated RegionsBase PairingBase SequenceEukaryotic CellsGenesProtein BindingProtein BiosynthesisProtein SubunitsRegulatory Sequences, Ribonucleic AcidRibosomesRNA, Ribosomal, 18S5' Untranslated RegionsProtein SubunitsRegulatory Sequences, Ribonucleic AcidRNA, Ribosomal, 18S

Identifiers

PMID15210968
PMCPMC470719
OpenAlexW1992814703

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.