Recon 2.2: from reconstruction to model of human metabolism
Recon 2.2: from reconstruction to model of human metabolism
About this item
Full title
Author / Creator
Swainston, Neil , Smallbone, Kieran , Hefzi, Hooman , Dobson, Paul D. , Brewer, Judy , Hanscho, Michael , Zielinski, Daniel C. , Ang, Kok Siong , Gardiner, Natalie J. , Gutierrez, Jahir M. , Kyriakopoulos, Sarantos , Lakshmanan, Meiyappan , Li, Shangzhong , Liu, Joanne K. , Martínez, Veronica S. , Orellana, Camila A. , Quek, Lake-Ee , Thomas, Alex , Zanghellini, Juergen , Borth, Nicole , Lee, Dong-Yup , Nielsen, Lars K. , Kell, Douglas B. , Lewis, Nathan E. and Mendes, Pedro
Publisher
New York: Springer US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Springer US
Subjects
More information
Scope and Contents
Contents
Introduction
The human genome-scale metabolic reconstruction details all known metabolic reactions occurring in humans, and thereby holds substantial promise for studying complex diseases and phenotypes. Capturing the whole human metabolic reconstruction is an on-going task and since the last community effort generated a consensus reconstruction, several updates have been developed.
Objectives
We report a new consensus version, Recon 2.2, which integrates various alternative versions with significant additional updates. In addition to re-establishing a consensus reconstruction, further key objectives included providing more comprehensive annotation of metabolites and genes, ensuring full mass and charge balance in all reactions, and developing a model that correctly predicts ATP production on a range of carbon sources.
Methods
Recon 2.2 has been developed through a combination of manual curation and automated error checking. Specific and significant manual updates include a respecification of fatty acid metabolism, oxidative phosphorylation and a coupling of the electron transport chain to ATP synthase activity. All metabolites have definitive chemical formulae and charges specified, and these are used to ensure full mass and charge reaction balancing through an automated linear programming approach. Additionally, improved integration with transcriptomics and proteomics data has been facilitated with the updated curation of relationships between genes, proteins and reactions.
Results
Recon 2.2 now represents the most predictive model of human metabolism to date as demonstrated here. Extensive manual curation has increased the reconstruction size to 5324 metabolites, 7785 reactions and 1675 associated genes, which now are mapped to a single standard. The focus upon mass and charge balancing of all reactions, along with better representation of energy generation, has produced a flux model that correctly predicts ATP yield on different carbon sources.
Conclusion
Through these updates we have achieved the most complete and best annotated consensus human metabolic reconstruction available, thereby increasing the ability of this resource to provide novel insights into normal and disease states in human. The model is freely available from the Biomodels database (
http://identifiers.org/biomodels.db/MODEL1603150001
)....
Alternative Titles
Full title
Recon 2.2: from reconstruction to model of human metabolism
Authors, Artists and Contributors
Author / Creator
Smallbone, Kieran
Hefzi, Hooman
Dobson, Paul D.
Brewer, Judy
Hanscho, Michael
Zielinski, Daniel C.
Ang, Kok Siong
Gardiner, Natalie J.
Gutierrez, Jahir M.
Kyriakopoulos, Sarantos
Lakshmanan, Meiyappan
Li, Shangzhong
Liu, Joanne K.
Martínez, Veronica S.
Orellana, Camila A.
Quek, Lake-Ee
Thomas, Alex
Zanghellini, Juergen
Borth, Nicole
Lee, Dong-Yup
Nielsen, Lars K.
Kell, Douglas B.
Lewis, Nathan E.
Mendes, Pedro
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4896983
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4896983
Other Identifiers
ISSN
1573-3882
E-ISSN
1573-3890
DOI
10.1007/s11306-016-1051-4