Cargando…

Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo

BACKGROUND: Genome-wide characterization of tissue- or cell-specific gene expression is a recurrent bottleneck in biology. We have developed a sensitive approach based on ultra-low RNA sequencing coupled to laser assisted microdissection for analyzing different tissues of the small Arabidopsis embry...

Descripción completa

Detalles Bibliográficos
Autores principales: Sakai, Kaori, Taconnat, Ludivine, Borrega, Nero, Yansouni, Jennifer, Brunaud, Véronique, Paysant-Le Roux, Christine, Delannoy, Etienne, Martin Magniette, Marie-Laure, Lepiniec, Loïc, Faure, Jean Denis, Balzergue, Sandrine, Dubreucq, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797369/
https://www.ncbi.nlm.nih.gov/pubmed/29434651
http://dx.doi.org/10.1186/s13007-018-0275-x
_version_ 1783297671325286400
author Sakai, Kaori
Taconnat, Ludivine
Borrega, Nero
Yansouni, Jennifer
Brunaud, Véronique
Paysant-Le Roux, Christine
Delannoy, Etienne
Martin Magniette, Marie-Laure
Lepiniec, Loïc
Faure, Jean Denis
Balzergue, Sandrine
Dubreucq, Bertrand
author_facet Sakai, Kaori
Taconnat, Ludivine
Borrega, Nero
Yansouni, Jennifer
Brunaud, Véronique
Paysant-Le Roux, Christine
Delannoy, Etienne
Martin Magniette, Marie-Laure
Lepiniec, Loïc
Faure, Jean Denis
Balzergue, Sandrine
Dubreucq, Bertrand
author_sort Sakai, Kaori
collection PubMed
description BACKGROUND: Genome-wide characterization of tissue- or cell-specific gene expression is a recurrent bottleneck in biology. We have developed a sensitive approach based on ultra-low RNA sequencing coupled to laser assisted microdissection for analyzing different tissues of the small Arabidopsis embryo. METHODS AND RESULTS: We first characterized the number of genes detected according to the quantity of tissue yield and total RNA extracted. Our results revealed that as low as 0.02 mm(2) of tissue and 50 pg of total RNA can be used without compromising the number of genes detected. The optimised protocol was used to compare the epidermal versus mesophyll cell transcriptomes of cotyledons at the torpedo-shaped stage of embryo development. The approach was validated by the recovery of well-known epidermal genes such AtML1 or AtPDF2 and genes involved in flavonoid and cuticular waxes pathways. Moreover, the interest and sensitivity of this approach were highlighted by the characterization of several transcription factors preferentially expressed in epidermal cells. CONCLUSION: This technical advance unlocks some current limitations of transcriptomic analyses and allows to investigate further and efficiently new biological questions for which only a very small amounts of cells need to be isolated. For instance, it paves the way to increasing the spatial accuracy of regulatory networks in developing small embryo of Arabidopsis or other plant tissues. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0275-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5797369
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-57973692018-02-12 Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo Sakai, Kaori Taconnat, Ludivine Borrega, Nero Yansouni, Jennifer Brunaud, Véronique Paysant-Le Roux, Christine Delannoy, Etienne Martin Magniette, Marie-Laure Lepiniec, Loïc Faure, Jean Denis Balzergue, Sandrine Dubreucq, Bertrand Plant Methods Methodology BACKGROUND: Genome-wide characterization of tissue- or cell-specific gene expression is a recurrent bottleneck in biology. We have developed a sensitive approach based on ultra-low RNA sequencing coupled to laser assisted microdissection for analyzing different tissues of the small Arabidopsis embryo. METHODS AND RESULTS: We first characterized the number of genes detected according to the quantity of tissue yield and total RNA extracted. Our results revealed that as low as 0.02 mm(2) of tissue and 50 pg of total RNA can be used without compromising the number of genes detected. The optimised protocol was used to compare the epidermal versus mesophyll cell transcriptomes of cotyledons at the torpedo-shaped stage of embryo development. The approach was validated by the recovery of well-known epidermal genes such AtML1 or AtPDF2 and genes involved in flavonoid and cuticular waxes pathways. Moreover, the interest and sensitivity of this approach were highlighted by the characterization of several transcription factors preferentially expressed in epidermal cells. CONCLUSION: This technical advance unlocks some current limitations of transcriptomic analyses and allows to investigate further and efficiently new biological questions for which only a very small amounts of cells need to be isolated. For instance, it paves the way to increasing the spatial accuracy of regulatory networks in developing small embryo of Arabidopsis or other plant tissues. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0275-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-03 /pmc/articles/PMC5797369/ /pubmed/29434651 http://dx.doi.org/10.1186/s13007-018-0275-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Sakai, Kaori
Taconnat, Ludivine
Borrega, Nero
Yansouni, Jennifer
Brunaud, Véronique
Paysant-Le Roux, Christine
Delannoy, Etienne
Martin Magniette, Marie-Laure
Lepiniec, Loïc
Faure, Jean Denis
Balzergue, Sandrine
Dubreucq, Bertrand
Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
title Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
title_full Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
title_fullStr Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
title_full_unstemmed Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
title_short Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
title_sort combining laser-assisted microdissection (lam) and rna-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of arabidopsis embryo
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797369/
https://www.ncbi.nlm.nih.gov/pubmed/29434651
http://dx.doi.org/10.1186/s13007-018-0275-x
work_keys_str_mv AT sakaikaori combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT taconnatludivine combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT borreganero combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT yansounijennifer combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT brunaudveronique combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT paysantlerouxchristine combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT delannoyetienne combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT martinmagniettemarielaure combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT lepiniecloic combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT faurejeandenis combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT balzerguesandrine combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo
AT dubreucqbertrand combininglaserassistedmicrodissectionlamandrnaseqallowstoperformacomprehensivetranscriptomicanalysisofepidermalcellsofarabidopsisembryo