Evidence map›Paper›PMID 24564391›Full record

ArticleBMC bioinformatics2013

Transcript features alone enable accurate prediction and understanding of gene expression in S. cerevisiae.

Hadas Zur, Tamir Tuller

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2013. 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
1.6field-weighted citation impact, top 16% 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, 29 citations in OpenAlex.

  1. Article
  2. Effective Gene Expression Prediction and Optimization from Protein Sequences.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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  8. Genome scale analysis of Escherichia coli with a comprehensive prokaryotic sequence-based biophysical model of translation initiation and elongation.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  9. RNA (New York, N.Y.) · 2017
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  13. Review
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  15. Modelling the efficiency of codon-tRNA interactions based on codon usage bias.DNA research : an international journal for rapid publication of reports on genes and genomes · 2014
    Article
  16. 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

2 authors at 1 institution in 1 country.

Hadas Zur
Tamir Tuller
Tel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene expression is a central process in all living organisms. Central questions in the field are related to the way the expression levels of genes are encoded in the transcripts and affect their evolution, and the potential to predict expression levels solely by transcript features. In this study we analyze S. cerevisiae, a model organism with the most abundant relevant cellular and genomic measurements, to evaluate the accuracy in which expression levels can be predicted by different parts of the transcript. To this end, we perform various types of regression analyses based on a total of 5323 features of the transcript. The main advantage of the proposed predictors over previous ones is related to the accurate and comprehensive definitions of the relevant transcript features, which are based on biophysical knowledge of the gene transcription and translation processes, their modeling and evolution.

resultsCross validation analyses of our predictors demonstrate that they achieve a correlation of 0.68/0.68/0.70/0.61/0.81 with mRNA levels, ribosomal density, protein levels, proteins per mRNA molecule (PPR), and ribosomal load (RL) respectively (all p-values <10(-140)). When we consider predictors that are based exclusively on the features related to different parts of the transcript (5'UTR, ORF, 3'UTR), the correlations with protein levels were 0.27/0.71/0.25 (all p-values <10(-5)), suggesting that the information in the UTRs is redundant, and features of the ORF alone yield similar predictions to the ones obtained based on the entire transcript.

conclusionsThe reported results demonstrate that in the analyzed model organism the expression levels of a gene are encoded in the transcript. Specifically, the prediction of a large fraction of the variance of the different gene expression steps based on transcript features alone is feasible in S. cerevisiae. We report dozens of novel transcript features related to expression levels predictions, demonstrating how such analyses can aid in understanding the gene expression process and its evolution, and how such predictors can be designed for other organisms in the future.

Indexed as

Gene Expression Regulation, FungalTranscription, Genetic3' Untranslated Regions5' Untranslated RegionsFungal ProteinsGene ExpressionNonlinear DynamicsProtein BiosynthesisRNA, MessengerSaccharomyces cerevisiae3' Untranslated Regions5' Untranslated RegionsFungal ProteinsRNA, Messenger

Identifiers

PMID24564391
PMCPMC3852043
OpenAlexW2132390360

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.