Cargando…
High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response
Sugars act not only as substrates for plant metabolism, but also have a pivotal role in signaling pathways. Glucose signaling has been widely studied in the vascular plant Arabidopsis thaliana, but it has remained unexplored in non-vascular species such as Physcomitrella patens. To investigate P. pa...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717569/ https://www.ncbi.nlm.nih.gov/pubmed/33275616 http://dx.doi.org/10.1371/journal.pone.0242919 |
_version_ | 1783619333888409600 |
---|---|
author | Chamorro-Flores, Alejandra Tiessen-Favier, Axel Gregorio-Jorge, Josefat Villalobos-López, Miguel Angel Guevara-García, Ángel Arturo López-Meyer, Melina Arroyo-Becerra, Analilia |
author_facet | Chamorro-Flores, Alejandra Tiessen-Favier, Axel Gregorio-Jorge, Josefat Villalobos-López, Miguel Angel Guevara-García, Ángel Arturo López-Meyer, Melina Arroyo-Becerra, Analilia |
author_sort | Chamorro-Flores, Alejandra |
collection | PubMed |
description | Sugars act not only as substrates for plant metabolism, but also have a pivotal role in signaling pathways. Glucose signaling has been widely studied in the vascular plant Arabidopsis thaliana, but it has remained unexplored in non-vascular species such as Physcomitrella patens. To investigate P. patens response to high glucose treatment, we explored the dynamic changes in metabolism and protein population by applying a metabolomic fingerprint analysis (DIESI-MS), carbohydrate and chlorophyll quantification, Fv/Fm determination and label-free untargeted proteomics. Glucose feeding causes specific changes in P. patens metabolomic fingerprint, carbohydrate contents and protein accumulation, which is clearly different from those of osmotically induced responses. The maximal rate of PSII was not affected although chlorophyll decreased in both treatments. The biological process, cellular component, and molecular function gene ontology (GO) classifications of the differentially expressed proteins indicate the translation process is the most represented category in response to glucose, followed by photosynthesis, cellular response to oxidative stress and protein refolding. Importantly, although several proteins have high fold changes, these proteins have no predicted identity. The most significant discovery of our study at the proteome level is that high glucose increase abundance of proteins related to the translation process, which was not previously evidenced in non-vascular plants, indicating that regulation by glucose at the translational level is a partially conserved response in both plant lineages. To our knowledge, this is the first time that metabolome fingerprint and proteomic analyses are performed after a high sugar treatment in non-vascular plants. These findings unravel evolutionarily shared and differential responses between vascular and non-vascular plants. |
format | Online Article Text |
id | pubmed-7717569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77175692020-12-09 High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response Chamorro-Flores, Alejandra Tiessen-Favier, Axel Gregorio-Jorge, Josefat Villalobos-López, Miguel Angel Guevara-García, Ángel Arturo López-Meyer, Melina Arroyo-Becerra, Analilia PLoS One Research Article Sugars act not only as substrates for plant metabolism, but also have a pivotal role in signaling pathways. Glucose signaling has been widely studied in the vascular plant Arabidopsis thaliana, but it has remained unexplored in non-vascular species such as Physcomitrella patens. To investigate P. patens response to high glucose treatment, we explored the dynamic changes in metabolism and protein population by applying a metabolomic fingerprint analysis (DIESI-MS), carbohydrate and chlorophyll quantification, Fv/Fm determination and label-free untargeted proteomics. Glucose feeding causes specific changes in P. patens metabolomic fingerprint, carbohydrate contents and protein accumulation, which is clearly different from those of osmotically induced responses. The maximal rate of PSII was not affected although chlorophyll decreased in both treatments. The biological process, cellular component, and molecular function gene ontology (GO) classifications of the differentially expressed proteins indicate the translation process is the most represented category in response to glucose, followed by photosynthesis, cellular response to oxidative stress and protein refolding. Importantly, although several proteins have high fold changes, these proteins have no predicted identity. The most significant discovery of our study at the proteome level is that high glucose increase abundance of proteins related to the translation process, which was not previously evidenced in non-vascular plants, indicating that regulation by glucose at the translational level is a partially conserved response in both plant lineages. To our knowledge, this is the first time that metabolome fingerprint and proteomic analyses are performed after a high sugar treatment in non-vascular plants. These findings unravel evolutionarily shared and differential responses between vascular and non-vascular plants. Public Library of Science 2020-12-04 /pmc/articles/PMC7717569/ /pubmed/33275616 http://dx.doi.org/10.1371/journal.pone.0242919 Text en © 2020 Chamorro-Flores et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chamorro-Flores, Alejandra Tiessen-Favier, Axel Gregorio-Jorge, Josefat Villalobos-López, Miguel Angel Guevara-García, Ángel Arturo López-Meyer, Melina Arroyo-Becerra, Analilia High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response |
title | High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response |
title_full | High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response |
title_fullStr | High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response |
title_full_unstemmed | High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response |
title_short | High levels of glucose alter Physcomitrella patens metabolism and trigger a differential proteomic response |
title_sort | high levels of glucose alter physcomitrella patens metabolism and trigger a differential proteomic response |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717569/ https://www.ncbi.nlm.nih.gov/pubmed/33275616 http://dx.doi.org/10.1371/journal.pone.0242919 |
work_keys_str_mv | AT chamorrofloresalejandra highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse AT tiessenfavieraxel highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse AT gregoriojorgejosefat highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse AT villaloboslopezmiguelangel highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse AT guevaragarciaangelarturo highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse AT lopezmeyermelina highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse AT arroyobecerraanalilia highlevelsofglucosealterphyscomitrellapatensmetabolismandtriggeradifferentialproteomicresponse |