Evidence map›Paper›PMID 12679518›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Isolation and identification of short nucleotide sequences that affect translation initiation in Saccharomyces cerevisiae.

Wei Zhou, Gerald M Edelman, Vincent P Mauro

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Synthetic polycistronic sequences in eukaryotes.Synthetic and systems biotechnology · 2021
    Review
  4. Synthetic biology: advancing the design of diverse genetic systems.Annual review of chemical and biomolecular engineering · 2013
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Searching for IRES.RNA (New York, N.Y.) · 2006
    Review
  11. An unusual internal ribosome entry site in the herpes simplex virus thymidine kinase gene.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  12. A positive feedback vector for identification of nucleotide sequences that enhance translation.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  13. Biochemical and functional analysis of a 9-nt RNA sequence that affects translation efficiency in eukaryotic cells.Proceedings of the National Academy of Sciences of the United States of America · 2004
    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

3 authors at 1 institution in 1 country.

Wei ZhouDepartment 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

REGULATION OF NEURAL CAMS BY GROWTH FACTORS AND ACTIVITYR01NS039837 · NINDS · SCRIPPS RESEARCH INSTITUTE · PI EDELMAN, GERALD · 2000 to 2003
$1.3M
Internal Initiation in the Translation of Cellular mRNAsR01GM061725 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI MAURO, VINCENT P · 2001 to 2004
$1.2M
NIGMS NIH HHS GM61725NIGMS NIH HHS R01 GM061725NINDS NIH HHS NS39837NINDS NIH HHS R01 NS039837
6 · The paper itself

Abstract

In previous studies, we demonstrated the sufficiency of short nucleotide sequences to facilitate internal initiation of translation in mammalian cells. By using a selection methodology, we have now identified comparable sequences in Saccharomyces cerevisiae. For these studies, a library of constructs expressing dicistronic mRNAs with the HIS3 gene as the second cistron and 18 random nucleotides in the intercistronic region was introduced into a yeast strain in which the endogenous HIS3 gene was deleted. Untransformed cells or those containing the parent construct failed to grow on medium lacking histidine. Intercistronic sequences recovered from cells that did grow were evaluated by using various criteria. Fifty-six of the 18-nt sequences (approximately 1/400,000) functioned as synthetic internal ribosome entry sites (IRESes). The 14 most active sequences allowed growth in the presence of 0.1-0.6 mM 3-amino-1,2,4-triazole, a competitive inhibitor of the HIS3 gene product. In addition, eight sequences were identified that were not IRESes, but that enhanced HIS3 expression by an alternative mechanism that depended on the 5' end of the mRNA and appeared to involve either shunting or reinitiation. Comparisons among the 56 selected IRESes identified eight significant sequence matches containing up to 10 nucleotides. Many of the selected sequences also contained extensive complementary matches to yeast 18S rRNA, some at overlapping sites. The identification of cis sequences that facilitate translation initiation in yeast enables detailed biochemical and genetic analyses of underlying mechanisms and may have practical applications for bioengineering.

Indexed as

Base SequenceGenes, FungalHydro-LyasesPeptide Chain Initiation, TranslationalRNA, FungalRNA, MessengerSaccharomyces cerevisiaeHydro-Lyasesimidazoleglycerolphosphate dehydrataseRNA, FungalRNA, Messenger

Identifiers

PMID12679518
PMCPMC153577
OpenAlexW2103008797

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.