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Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures

Transcript profiling has shown the molecular bases of several biological processes in plants but few studies have developed an understanding of overall transcriptome variation. We investigated transcriptome structure in white spruce (Picea glauca), aiming to delineate its modular organization and as...

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Autores principales: Raherison, Elie S. M., Giguère, Isabelle, Caron, Sébastien, Lamara, Mebarek, MacKay, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024012/
https://www.ncbi.nlm.nih.gov/pubmed/25728802
http://dx.doi.org/10.1111/nph.13343
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author Raherison, Elie S. M.
Giguère, Isabelle
Caron, Sébastien
Lamara, Mebarek
MacKay, John J.
author_facet Raherison, Elie S. M.
Giguère, Isabelle
Caron, Sébastien
Lamara, Mebarek
MacKay, John J.
author_sort Raherison, Elie S. M.
collection PubMed
description Transcript profiling has shown the molecular bases of several biological processes in plants but few studies have developed an understanding of overall transcriptome variation. We investigated transcriptome structure in white spruce (Picea glauca), aiming to delineate its modular organization and associated functional and evolutionary attributes. Microarray analyses were used to: identify and functionally characterize groups of co‐expressed genes; investigate expressional and functional diversity of vascular tissue preferential genes which were conserved among Picea species, and identify expression networks underlying wood formation. We classified 22 857 genes as variable (79%; 22 coexpression groups) or invariant (21%) by profiling across several vegetative tissues. Modular organization and complex transcriptome restructuring among vascular tissue preferential genes was revealed by their assignment to coexpression groups with partially overlapping profiles and partially distinct functions. Integrated analyses of tissue‐based and temporally variable profiles identified secondary xylem gene networks, showed their remodelling over a growing season and identified PgNAC‐7 (no apical meristerm (NAM), Arabidopsis transcription activation factor (ATAF) and cup‐shaped cotyledon (CUC) transcription factor 007 in Picea glauca) as a major hub gene specific to earlywood formation. Reference profiling identified comprehensive, statistically robust coexpressed groups, revealing that modular organization underpins the evolutionary conservation of the transcriptome structure.
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spelling pubmed-50240122016-09-23 Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures Raherison, Elie S. M. Giguère, Isabelle Caron, Sébastien Lamara, Mebarek MacKay, John J. New Phytol Research Transcript profiling has shown the molecular bases of several biological processes in plants but few studies have developed an understanding of overall transcriptome variation. We investigated transcriptome structure in white spruce (Picea glauca), aiming to delineate its modular organization and associated functional and evolutionary attributes. Microarray analyses were used to: identify and functionally characterize groups of co‐expressed genes; investigate expressional and functional diversity of vascular tissue preferential genes which were conserved among Picea species, and identify expression networks underlying wood formation. We classified 22 857 genes as variable (79%; 22 coexpression groups) or invariant (21%) by profiling across several vegetative tissues. Modular organization and complex transcriptome restructuring among vascular tissue preferential genes was revealed by their assignment to coexpression groups with partially overlapping profiles and partially distinct functions. Integrated analyses of tissue‐based and temporally variable profiles identified secondary xylem gene networks, showed their remodelling over a growing season and identified PgNAC‐7 (no apical meristerm (NAM), Arabidopsis transcription activation factor (ATAF) and cup‐shaped cotyledon (CUC) transcription factor 007 in Picea glauca) as a major hub gene specific to earlywood formation. Reference profiling identified comprehensive, statistically robust coexpressed groups, revealing that modular organization underpins the evolutionary conservation of the transcriptome structure. John Wiley and Sons Inc. 2015-07 2015-02-27 /pmc/articles/PMC5024012/ /pubmed/25728802 http://dx.doi.org/10.1111/nph.13343 Text en © 2015 The Authors. New Phytologist © 2015 New Phytologist Trust This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Raherison, Elie S. M.
Giguère, Isabelle
Caron, Sébastien
Lamara, Mebarek
MacKay, John J.
Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures
title Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures
title_full Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures
title_fullStr Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures
title_full_unstemmed Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures
title_short Modular organization of the white spruce (Picea glauca) transcriptome reveals functional organization and evolutionary signatures
title_sort modular organization of the white spruce (picea glauca) transcriptome reveals functional organization and evolutionary signatures
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024012/
https://www.ncbi.nlm.nih.gov/pubmed/25728802
http://dx.doi.org/10.1111/nph.13343
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