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Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon

Lignin biosynthesis begins with the deamination of phenylalanine and tyrosine (Tyr) as a key branch point between primary and secondary metabolism in land plants. Here, we used a systems biology approach to investigate the global metabolic responses to lignin pathway perturbations in the model grass...

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Autores principales: Barros, Jaime, Shrestha, Him K, Serrani-Yarce, Juan C, Engle, Nancy L, Abraham, Paul E, Tschaplinski, Timothy J, Hettich, Robert L, Dixon, Richard A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421481/
https://www.ncbi.nlm.nih.gov/pubmed/35670759
http://dx.doi.org/10.1093/plcell/koac171
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author Barros, Jaime
Shrestha, Him K
Serrani-Yarce, Juan C
Engle, Nancy L
Abraham, Paul E
Tschaplinski, Timothy J
Hettich, Robert L
Dixon, Richard A
author_facet Barros, Jaime
Shrestha, Him K
Serrani-Yarce, Juan C
Engle, Nancy L
Abraham, Paul E
Tschaplinski, Timothy J
Hettich, Robert L
Dixon, Richard A
author_sort Barros, Jaime
collection PubMed
description Lignin biosynthesis begins with the deamination of phenylalanine and tyrosine (Tyr) as a key branch point between primary and secondary metabolism in land plants. Here, we used a systems biology approach to investigate the global metabolic responses to lignin pathway perturbations in the model grass Brachypodium distachyon. We identified the lignin biosynthetic protein families and found that ammonia-lyases (ALs) are among the most abundant proteins in lignifying tissues in grasses. Integrated metabolomic and proteomic data support a link between lignin biosynthesis and primary metabolism mediated by the ammonia released from ALs that is recycled for the synthesis of amino acids via glutamine. RNA interference knockdown of lignin genes confirmed that the route of the canonical pathway using shikimate ester intermediates is not essential for lignin formation in Brachypodium, and there is an alternative pathway from Tyr via sinapic acid for the synthesis of syringyl lignin involving yet uncharacterized enzymatic steps. Our findings support a model in which plant ALs play a central role in coordinating the allocation of carbon for lignin synthesis and the nitrogen available for plant growth. Collectively, these data also emphasize the value of integrative multiomic analyses to advance our understanding of plant metabolism.
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spelling pubmed-94214812022-08-29 Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon Barros, Jaime Shrestha, Him K Serrani-Yarce, Juan C Engle, Nancy L Abraham, Paul E Tschaplinski, Timothy J Hettich, Robert L Dixon, Richard A Plant Cell Research Articles Lignin biosynthesis begins with the deamination of phenylalanine and tyrosine (Tyr) as a key branch point between primary and secondary metabolism in land plants. Here, we used a systems biology approach to investigate the global metabolic responses to lignin pathway perturbations in the model grass Brachypodium distachyon. We identified the lignin biosynthetic protein families and found that ammonia-lyases (ALs) are among the most abundant proteins in lignifying tissues in grasses. Integrated metabolomic and proteomic data support a link between lignin biosynthesis and primary metabolism mediated by the ammonia released from ALs that is recycled for the synthesis of amino acids via glutamine. RNA interference knockdown of lignin genes confirmed that the route of the canonical pathway using shikimate ester intermediates is not essential for lignin formation in Brachypodium, and there is an alternative pathway from Tyr via sinapic acid for the synthesis of syringyl lignin involving yet uncharacterized enzymatic steps. Our findings support a model in which plant ALs play a central role in coordinating the allocation of carbon for lignin synthesis and the nitrogen available for plant growth. Collectively, these data also emphasize the value of integrative multiomic analyses to advance our understanding of plant metabolism. Oxford University Press 2022-06-07 /pmc/articles/PMC9421481/ /pubmed/35670759 http://dx.doi.org/10.1093/plcell/koac171 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Barros, Jaime
Shrestha, Him K
Serrani-Yarce, Juan C
Engle, Nancy L
Abraham, Paul E
Tschaplinski, Timothy J
Hettich, Robert L
Dixon, Richard A
Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon
title Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon
title_full Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon
title_fullStr Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon
title_full_unstemmed Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon
title_short Proteomic and metabolic disturbances in lignin-modified Brachypodium distachyon
title_sort proteomic and metabolic disturbances in lignin-modified brachypodium distachyon
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421481/
https://www.ncbi.nlm.nih.gov/pubmed/35670759
http://dx.doi.org/10.1093/plcell/koac171
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