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Essential metabolism for a minimal cell

JCVI-syn3A, a robust minimal cell with a 543 kbp genome and 493 genes, provides a versatile platform to study the basics of life. Using the vast amount of experimental information available on its precursor, Mycoplasma mycoides capri, we assembled a near-complete metabolic network with 98% of enzyma...

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Autores principales: Breuer, Marian, Earnest, Tyler M, Merryman, Chuck, Wise, Kim S, Sun, Lijie, Lynott, Michaela R, Hutchison, Clyde A, Smith, Hamilton O, Lapek, John D, Gonzalez, David J, de Crécy-Lagard, Valérie, Haas, Drago, Hanson, Andrew D, Labhsetwar, Piyush, Glass, John I, Luthey-Schulten, Zaida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609329/
https://www.ncbi.nlm.nih.gov/pubmed/30657448
http://dx.doi.org/10.7554/eLife.36842
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author Breuer, Marian
Earnest, Tyler M
Merryman, Chuck
Wise, Kim S
Sun, Lijie
Lynott, Michaela R
Hutchison, Clyde A
Smith, Hamilton O
Lapek, John D
Gonzalez, David J
de Crécy-Lagard, Valérie
Haas, Drago
Hanson, Andrew D
Labhsetwar, Piyush
Glass, John I
Luthey-Schulten, Zaida
author_facet Breuer, Marian
Earnest, Tyler M
Merryman, Chuck
Wise, Kim S
Sun, Lijie
Lynott, Michaela R
Hutchison, Clyde A
Smith, Hamilton O
Lapek, John D
Gonzalez, David J
de Crécy-Lagard, Valérie
Haas, Drago
Hanson, Andrew D
Labhsetwar, Piyush
Glass, John I
Luthey-Schulten, Zaida
author_sort Breuer, Marian
collection PubMed
description JCVI-syn3A, a robust minimal cell with a 543 kbp genome and 493 genes, provides a versatile platform to study the basics of life. Using the vast amount of experimental information available on its precursor, Mycoplasma mycoides capri, we assembled a near-complete metabolic network with 98% of enzymatic reactions supported by annotation or experiment. The model agrees well with genome-scale in vivo transposon mutagenesis experiments, showing a Matthews correlation coefficient of 0.59. The genes in the reconstruction have a high in vivo essentiality or quasi-essentiality of 92% (68% essential), compared to 79% in silico essentiality. This coherent model of the minimal metabolism in JCVI-syn3A at the same time also points toward specific open questions regarding the minimal genome of JCVI-syn3A, which still contains many genes of generic or completely unclear function. In particular, the model, its comparison to in vivo essentiality and proteomics data yield specific hypotheses on gene functions and metabolic capabilities; and provide suggestions for several further gene removals. In this way, the model and its accompanying data guide future investigations of the minimal cell. Finally, the identification of 30 essential genes with unclear function will motivate the search for new biological mechanisms beyond metabolism.
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spelling pubmed-66093292019-07-08 Essential metabolism for a minimal cell Breuer, Marian Earnest, Tyler M Merryman, Chuck Wise, Kim S Sun, Lijie Lynott, Michaela R Hutchison, Clyde A Smith, Hamilton O Lapek, John D Gonzalez, David J de Crécy-Lagard, Valérie Haas, Drago Hanson, Andrew D Labhsetwar, Piyush Glass, John I Luthey-Schulten, Zaida eLife Computational and Systems Biology JCVI-syn3A, a robust minimal cell with a 543 kbp genome and 493 genes, provides a versatile platform to study the basics of life. Using the vast amount of experimental information available on its precursor, Mycoplasma mycoides capri, we assembled a near-complete metabolic network with 98% of enzymatic reactions supported by annotation or experiment. The model agrees well with genome-scale in vivo transposon mutagenesis experiments, showing a Matthews correlation coefficient of 0.59. The genes in the reconstruction have a high in vivo essentiality or quasi-essentiality of 92% (68% essential), compared to 79% in silico essentiality. This coherent model of the minimal metabolism in JCVI-syn3A at the same time also points toward specific open questions regarding the minimal genome of JCVI-syn3A, which still contains many genes of generic or completely unclear function. In particular, the model, its comparison to in vivo essentiality and proteomics data yield specific hypotheses on gene functions and metabolic capabilities; and provide suggestions for several further gene removals. In this way, the model and its accompanying data guide future investigations of the minimal cell. Finally, the identification of 30 essential genes with unclear function will motivate the search for new biological mechanisms beyond metabolism. eLife Sciences Publications, Ltd 2019-01-18 /pmc/articles/PMC6609329/ /pubmed/30657448 http://dx.doi.org/10.7554/eLife.36842 Text en © 2019, Breuer et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Breuer, Marian
Earnest, Tyler M
Merryman, Chuck
Wise, Kim S
Sun, Lijie
Lynott, Michaela R
Hutchison, Clyde A
Smith, Hamilton O
Lapek, John D
Gonzalez, David J
de Crécy-Lagard, Valérie
Haas, Drago
Hanson, Andrew D
Labhsetwar, Piyush
Glass, John I
Luthey-Schulten, Zaida
Essential metabolism for a minimal cell
title Essential metabolism for a minimal cell
title_full Essential metabolism for a minimal cell
title_fullStr Essential metabolism for a minimal cell
title_full_unstemmed Essential metabolism for a minimal cell
title_short Essential metabolism for a minimal cell
title_sort essential metabolism for a minimal cell
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609329/
https://www.ncbi.nlm.nih.gov/pubmed/30657448
http://dx.doi.org/10.7554/eLife.36842
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