Cargando…

Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice

Crown roots constitute the main part of the rice root system. Several key genes involved in crown root initiation and development have been identified by functional genomics approaches. Nevertheless, these approaches are impaired by functional redundancy and mutant lethality. To overcome these limit...

Descripción completa

Detalles Bibliográficos
Autores principales: Lavarenne, Jérémy, Gonin, Mathieu, Champion, Antony, Javelle, Marie, Adam, Hélène, Rouster, Jacques, Conejéro, Geneviève, Lartaud, Marc, Verdeil, Jean-Luc, Laplaze, Laurent, Sallaud, Christophe, Lucas, Mikael, Gantet, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676735/
https://www.ncbi.nlm.nih.gov/pubmed/33211715
http://dx.doi.org/10.1371/journal.pone.0238736
_version_ 1783611833929695232
author Lavarenne, Jérémy
Gonin, Mathieu
Champion, Antony
Javelle, Marie
Adam, Hélène
Rouster, Jacques
Conejéro, Geneviève
Lartaud, Marc
Verdeil, Jean-Luc
Laplaze, Laurent
Sallaud, Christophe
Lucas, Mikael
Gantet, Pascal
author_facet Lavarenne, Jérémy
Gonin, Mathieu
Champion, Antony
Javelle, Marie
Adam, Hélène
Rouster, Jacques
Conejéro, Geneviève
Lartaud, Marc
Verdeil, Jean-Luc
Laplaze, Laurent
Sallaud, Christophe
Lucas, Mikael
Gantet, Pascal
author_sort Lavarenne, Jérémy
collection PubMed
description Crown roots constitute the main part of the rice root system. Several key genes involved in crown root initiation and development have been identified by functional genomics approaches. Nevertheless, these approaches are impaired by functional redundancy and mutant lethality. To overcome these limitations, organ targeted transcriptome analysis can help to identify genes involved in crown root formation and early development. In this study, we generated an atlas of genes expressed in developing crown root primordia in comparison with adjacent stem cortical tissue at three different developmental stages before emergence, using laser capture microdissection. We identified 3975 genes differentially expressed in crown root primordia. About 30% of them were expressed at the three developmental stages, whereas 10.5%, 19.5% and 12.8% were specifically expressed at the early, intermediate and late stages, respectively. Sorting them by functional ontology highlighted an active transcriptional switch during the process of crown root primordia formation. Cross-analysis with other rice root development-related datasets revealed genes encoding transcription factors, chromatin remodeling factors, peptide growth factors, and cell wall remodeling enzymes that are likely to play a key role during crown root primordia formation. This atlas constitutes an open primary data resource for further studies on the regulation of crown root initiation and development.
format Online
Article
Text
id pubmed-7676735
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-76767352020-12-02 Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice Lavarenne, Jérémy Gonin, Mathieu Champion, Antony Javelle, Marie Adam, Hélène Rouster, Jacques Conejéro, Geneviève Lartaud, Marc Verdeil, Jean-Luc Laplaze, Laurent Sallaud, Christophe Lucas, Mikael Gantet, Pascal PLoS One Research Article Crown roots constitute the main part of the rice root system. Several key genes involved in crown root initiation and development have been identified by functional genomics approaches. Nevertheless, these approaches are impaired by functional redundancy and mutant lethality. To overcome these limitations, organ targeted transcriptome analysis can help to identify genes involved in crown root formation and early development. In this study, we generated an atlas of genes expressed in developing crown root primordia in comparison with adjacent stem cortical tissue at three different developmental stages before emergence, using laser capture microdissection. We identified 3975 genes differentially expressed in crown root primordia. About 30% of them were expressed at the three developmental stages, whereas 10.5%, 19.5% and 12.8% were specifically expressed at the early, intermediate and late stages, respectively. Sorting them by functional ontology highlighted an active transcriptional switch during the process of crown root primordia formation. Cross-analysis with other rice root development-related datasets revealed genes encoding transcription factors, chromatin remodeling factors, peptide growth factors, and cell wall remodeling enzymes that are likely to play a key role during crown root primordia formation. This atlas constitutes an open primary data resource for further studies on the regulation of crown root initiation and development. Public Library of Science 2020-11-19 /pmc/articles/PMC7676735/ /pubmed/33211715 http://dx.doi.org/10.1371/journal.pone.0238736 Text en © 2020 Lavarenne 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
Lavarenne, Jérémy
Gonin, Mathieu
Champion, Antony
Javelle, Marie
Adam, Hélène
Rouster, Jacques
Conejéro, Geneviève
Lartaud, Marc
Verdeil, Jean-Luc
Laplaze, Laurent
Sallaud, Christophe
Lucas, Mikael
Gantet, Pascal
Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
title Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
title_full Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
title_fullStr Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
title_full_unstemmed Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
title_short Transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
title_sort transcriptome profiling of laser-captured crown root primordia reveals new pathways activated during early stages of crown root formation in rice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676735/
https://www.ncbi.nlm.nih.gov/pubmed/33211715
http://dx.doi.org/10.1371/journal.pone.0238736
work_keys_str_mv AT lavarennejeremy transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT goninmathieu transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT championantony transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT javellemarie transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT adamhelene transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT rousterjacques transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT conejerogenevieve transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT lartaudmarc transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT verdeiljeanluc transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT laplazelaurent transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT sallaudchristophe transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT lucasmikael transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice
AT gantetpascal transcriptomeprofilingoflasercapturedcrownrootprimordiarevealsnewpathwaysactivatedduringearlystagesofcrownrootformationinrice