Evidence map›Paper›PMID 21685093›Full record

ArticleBioinformatics (Oxford, England)2011

Detection and interpretation of metabolite-transcript coresponses using combined profiling data.

Henning Redestig, Ivan G Costa

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Integrative metabolomics-genomics approach reveals key metabolic pathways and regulators of Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2022
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  12. Cellular and Molecular Responses ofFrontiers in microbiology · 2018
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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Henning RedestigRIKEN Plant Science Center, Yokohama, Japan. henning@psc.riken.jp
Ivan G Costa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationStudying the interplay between gene expression and metabolite levels can yield important information on the physiology of stress responses and adaptation strategies. Performing transcriptomics and metabolomics in parallel during time-series experiments represents a systematic way to gain such information. Several combined profiling datasets have been added to the public domain and they form a valuable resource for hypothesis generating studies. Unfortunately, detecting coresponses between transcript levels and metabolite abundances is non-trivial: they cannot be assumed to overlap directly with underlying biochemical pathways and they may be subject to time delays and obscured by considerable noise.

resultsOur aim was to predict pathway comemberships between metabolites and genes based on their coresponses to applied stress. We found that in the presence of strong noise and time-shifted responses, a hidden Markov model-based similarity outperforms the simpler Pearson correlation but performs comparably or worse in their absence. Therefore, we propose a supervised method that applies pathway information to summarize similarity statistics to a consensus statistic that is more informative than any of the single measures. Using four combined profiling datasets, we show that comembership between metabolites and genes can be predicted for numerous KEGG pathways; this opens opportunities for the detection of transcriptionally regulated pathways and novel metabolically related genes. AVAILABILITY: A command-line software tool is available at http://www.cin.ufpe.br/~igcf/Metabolites. CONTACT: henning@psc.riken.jp; igcf@cin.ufpe.br

Indexed as

Gene Expression ProfilingMetabolic Networks and PathwaysMetabolomicsModels, StatisticalAdaptation, PhysiologicalArabidopsisComputational BiologyMarkov ChainsSoftware

Identifiers

PMID21685093
PMCPMC3117345

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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.