Cargando…
Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum
Abiotic and biotic stresses widely reduce light harvesting complex (LHC) gene expression in higher plants and algae. However, control mechanisms and functions of these changes are not well understood. During herbivory, marine diatom species release oxylipins that impair grazer reproduction and serve...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005025/ https://www.ncbi.nlm.nih.gov/pubmed/32029835 http://dx.doi.org/10.1038/s41598-020-58885-9 |
_version_ | 1783494843744387072 |
---|---|
author | Islam, Shahima Sabharwal, Tanya Wu, Samantha Bullock, T. J. Mehdy, Mona C. |
author_facet | Islam, Shahima Sabharwal, Tanya Wu, Samantha Bullock, T. J. Mehdy, Mona C. |
author_sort | Islam, Shahima |
collection | PubMed |
description | Abiotic and biotic stresses widely reduce light harvesting complex (LHC) gene expression in higher plants and algae. However, control mechanisms and functions of these changes are not well understood. During herbivory, marine diatom species release oxylipins that impair grazer reproduction and serve as signaling molecules to nearby undamaged diatoms. To examine LHC mRNA regulation by oxylipin exposure, the diatom Phaeodactylum tricornutum was treated with a sublethal concentration of trans,trans-2,4-decadienal (DD) during the light cycle. Transcriptome analyses revealed extensive suppression of LHC mRNAs and a smaller set of up-regulated LHC mRNAs at 3 h. For two divergently regulated LHCF antennae family mRNAs, in vivo 4-thiouracil metabolic labeling was used to distinguish synthesis and degradation rates. Within 3 h of DD exposure, Lhcf2 mRNA levels and transcription were strongly suppressed and its mRNA half-life decreased. In contrast, Lhcf15 mRNA mainly accumulated between 3–9 h, its transcription increased and its mRNA was highly stabilized. Hence, DD-treated cells utilized transcriptional and mRNA stability control mechanisms which were likely major factors in the differing Lhcf2 and Lhcf15 expression patterns. Widespread LHC mRNA regulation and possible effects on photosynthesis may contribute to enhanced fitness in cells impacted by herbivory and other stresses. |
format | Online Article Text |
id | pubmed-7005025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70050252020-02-14 Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum Islam, Shahima Sabharwal, Tanya Wu, Samantha Bullock, T. J. Mehdy, Mona C. Sci Rep Article Abiotic and biotic stresses widely reduce light harvesting complex (LHC) gene expression in higher plants and algae. However, control mechanisms and functions of these changes are not well understood. During herbivory, marine diatom species release oxylipins that impair grazer reproduction and serve as signaling molecules to nearby undamaged diatoms. To examine LHC mRNA regulation by oxylipin exposure, the diatom Phaeodactylum tricornutum was treated with a sublethal concentration of trans,trans-2,4-decadienal (DD) during the light cycle. Transcriptome analyses revealed extensive suppression of LHC mRNAs and a smaller set of up-regulated LHC mRNAs at 3 h. For two divergently regulated LHCF antennae family mRNAs, in vivo 4-thiouracil metabolic labeling was used to distinguish synthesis and degradation rates. Within 3 h of DD exposure, Lhcf2 mRNA levels and transcription were strongly suppressed and its mRNA half-life decreased. In contrast, Lhcf15 mRNA mainly accumulated between 3–9 h, its transcription increased and its mRNA was highly stabilized. Hence, DD-treated cells utilized transcriptional and mRNA stability control mechanisms which were likely major factors in the differing Lhcf2 and Lhcf15 expression patterns. Widespread LHC mRNA regulation and possible effects on photosynthesis may contribute to enhanced fitness in cells impacted by herbivory and other stresses. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7005025/ /pubmed/32029835 http://dx.doi.org/10.1038/s41598-020-58885-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Islam, Shahima Sabharwal, Tanya Wu, Samantha Bullock, T. J. Mehdy, Mona C. Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum |
title | Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum |
title_full | Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum |
title_fullStr | Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum |
title_full_unstemmed | Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum |
title_short | Early dynamics of photosynthetic Lhcf2 and Lhcf15 transcription and mRNA stabilities in response to herbivory-related decadienal in Phaeodactylum tricornutum |
title_sort | early dynamics of photosynthetic lhcf2 and lhcf15 transcription and mrna stabilities in response to herbivory-related decadienal in phaeodactylum tricornutum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005025/ https://www.ncbi.nlm.nih.gov/pubmed/32029835 http://dx.doi.org/10.1038/s41598-020-58885-9 |
work_keys_str_mv | AT islamshahima earlydynamicsofphotosyntheticlhcf2andlhcf15transcriptionandmrnastabilitiesinresponsetoherbivoryrelateddecadienalinphaeodactylumtricornutum AT sabharwaltanya earlydynamicsofphotosyntheticlhcf2andlhcf15transcriptionandmrnastabilitiesinresponsetoherbivoryrelateddecadienalinphaeodactylumtricornutum AT wusamantha earlydynamicsofphotosyntheticlhcf2andlhcf15transcriptionandmrnastabilitiesinresponsetoherbivoryrelateddecadienalinphaeodactylumtricornutum AT bullocktj earlydynamicsofphotosyntheticlhcf2andlhcf15transcriptionandmrnastabilitiesinresponsetoherbivoryrelateddecadienalinphaeodactylumtricornutum AT mehdymonac earlydynamicsofphotosyntheticlhcf2andlhcf15transcriptionandmrnastabilitiesinresponsetoherbivoryrelateddecadienalinphaeodactylumtricornutum |