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dc.contributor.authorYilmaz, L. Safak
dc.contributor.authorLi, Xuhang
dc.contributor.authorNanda, Shivani
dc.contributor.authorFox, Bennett
dc.contributor.authorSchroeder, Frank
dc.contributor.authorWalhout, Albertha J M
dc.date2022-08-11T08:09:57.000
dc.date.accessioned2022-08-23T16:50:19Z
dc.date.available2022-08-23T16:50:19Z
dc.date.issued2020-10-06
dc.date.submitted2020-12-16
dc.identifier.citation<p>Mol Syst Biol. 2020 Oct;16(10):e9649. doi: 10.15252/msb.20209649. <a href="https://doi.org/10.15252/msb.20209649">Link to article on publisher's site</a></p>
dc.identifier.issn1744-4292 (Linking)
dc.identifier.doi10.15252/msb.20209649
dc.identifier.pmid33022146
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41639
dc.description.abstractMetabolism is a highly compartmentalized process that provides building blocks for biomass generation during development, homeostasis, and wound healing, and energy to support cellular and organismal processes. In metazoans, different cells and tissues specialize in different aspects of metabolism. However, studying the compartmentalization of metabolism in different cell types in a whole animal and for a particular stage of life is difficult. Here, we present MEtabolic models Reconciled with Gene Expression (MERGE), a computational pipeline that we used to predict tissue-relevant metabolic function at the network, pathway, reaction, and metabolite levels based on single-cell RNA-sequencing (scRNA-seq) data from the nematode Caenorhabditis elegans. Our analysis recapitulated known tissue functions in C. elegans, captured metabolic properties that are shared with similar tissues in human, and provided predictions for novel metabolic functions. MERGE is versatile and applicable to other systems. We envision this work as a starting point for the development of metabolic network models for individual cells as scRNA-seq continues to provide higher-resolution gene expression data.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=33022146&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright 2020 The Authors. This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCaenorhabditis elegans
dc.subjectdata integration
dc.subjectmetabolic network
dc.subjectsingle-cell RNA-seq
dc.subjecttissue metabolism
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.subjectComputational Biology
dc.subjectMolecular Biology
dc.subjectSystems Biology
dc.titleModeling tissue-relevant Caenorhabditis elegans metabolism at network, pathway, reaction, and metabolite levels
dc.typeJournal Article
dc.source.journaltitleMolecular systems biology
dc.source.volume16
dc.source.issue10
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5460&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/4430
dc.identifier.contextkey20637426
refterms.dateFOA2022-08-23T16:50:20Z
html.description.abstract<p>Metabolism is a highly compartmentalized process that provides building blocks for biomass generation during development, homeostasis, and wound healing, and energy to support cellular and organismal processes. In metazoans, different cells and tissues specialize in different aspects of metabolism. However, studying the compartmentalization of metabolism in different cell types in a whole animal and for a particular stage of life is difficult. Here, we present MEtabolic models Reconciled with Gene Expression (MERGE), a computational pipeline that we used to predict tissue-relevant metabolic function at the network, pathway, reaction, and metabolite levels based on single-cell RNA-sequencing (scRNA-seq) data from the nematode Caenorhabditis elegans. Our analysis recapitulated known tissue functions in C. elegans, captured metabolic properties that are shared with similar tissues in human, and provided predictions for novel metabolic functions. MERGE is versatile and applicable to other systems. We envision this work as a starting point for the development of metabolic network models for individual cells as scRNA-seq continues to provide higher-resolution gene expression data.</p>
dc.identifier.submissionpathoapubs/4430
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentProgram in Systems Biology
dc.source.pagese9649


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Copyright 2020 The Authors. This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as Copyright 2020 The Authors. This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.