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Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation

The circadian clock regulates physiological processes central to growth and survival. To date, most plant circadian clock studies have relied on diurnal transcriptome changes to elucidate molecular connections between the circadian clock and observable phenotypes in wild-type plants. Here, we have i...

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Autores principales: Graf, Alexander, Coman, Diana, Uhrig, R. Glen, Walsh, Sean, Flis, Anna, Stitt, Mark, Gruissem, Wilhelm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376707/
https://www.ncbi.nlm.nih.gov/pubmed/28250106
http://dx.doi.org/10.1098/rsob.160333
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author Graf, Alexander
Coman, Diana
Uhrig, R. Glen
Walsh, Sean
Flis, Anna
Stitt, Mark
Gruissem, Wilhelm
author_facet Graf, Alexander
Coman, Diana
Uhrig, R. Glen
Walsh, Sean
Flis, Anna
Stitt, Mark
Gruissem, Wilhelm
author_sort Graf, Alexander
collection PubMed
description The circadian clock regulates physiological processes central to growth and survival. To date, most plant circadian clock studies have relied on diurnal transcriptome changes to elucidate molecular connections between the circadian clock and observable phenotypes in wild-type plants. Here, we have integrated RNA-sequencing and protein mass spectrometry data to comparatively analyse the lhycca1, prr7prr9, gi and toc1 circadian clock mutant rosette at the end of day and end of night. Each mutant affects specific sets of genes and proteins, suggesting that the circadian clock regulation is modular. Furthermore, each circadian clock mutant maintains its own dynamically fluctuating transcriptome and proteome profile specific to subcellular compartments. Most of the measured protein levels do not correlate with changes in their corresponding transcripts. Transcripts and proteins that have coordinated changes in abundance are enriched for carbohydrate- and cold-responsive genes. Transcriptome changes in all four circadian clock mutants also affect genes encoding starch degradation enzymes, transcription factors and protein kinases. The comprehensive transcriptome and proteome datasets demonstrate that future system-driven research of the circadian clock requires multi-level experimental approaches. Our work also shows that further work is needed to elucidate the roles of post-translational modifications and protein degradation in the regulation of clock-related processes.
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spelling pubmed-53767072017-04-06 Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation Graf, Alexander Coman, Diana Uhrig, R. Glen Walsh, Sean Flis, Anna Stitt, Mark Gruissem, Wilhelm Open Biol Research The circadian clock regulates physiological processes central to growth and survival. To date, most plant circadian clock studies have relied on diurnal transcriptome changes to elucidate molecular connections between the circadian clock and observable phenotypes in wild-type plants. Here, we have integrated RNA-sequencing and protein mass spectrometry data to comparatively analyse the lhycca1, prr7prr9, gi and toc1 circadian clock mutant rosette at the end of day and end of night. Each mutant affects specific sets of genes and proteins, suggesting that the circadian clock regulation is modular. Furthermore, each circadian clock mutant maintains its own dynamically fluctuating transcriptome and proteome profile specific to subcellular compartments. Most of the measured protein levels do not correlate with changes in their corresponding transcripts. Transcripts and proteins that have coordinated changes in abundance are enriched for carbohydrate- and cold-responsive genes. Transcriptome changes in all four circadian clock mutants also affect genes encoding starch degradation enzymes, transcription factors and protein kinases. The comprehensive transcriptome and proteome datasets demonstrate that future system-driven research of the circadian clock requires multi-level experimental approaches. Our work also shows that further work is needed to elucidate the roles of post-translational modifications and protein degradation in the regulation of clock-related processes. The Royal Society 2017-03-01 /pmc/articles/PMC5376707/ /pubmed/28250106 http://dx.doi.org/10.1098/rsob.160333 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Graf, Alexander
Coman, Diana
Uhrig, R. Glen
Walsh, Sean
Flis, Anna
Stitt, Mark
Gruissem, Wilhelm
Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
title Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
title_full Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
title_fullStr Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
title_full_unstemmed Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
title_short Parallel analysis of Arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
title_sort parallel analysis of arabidopsis circadian clock mutants reveals different scales of transcriptome and proteome regulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376707/
https://www.ncbi.nlm.nih.gov/pubmed/28250106
http://dx.doi.org/10.1098/rsob.160333
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