Cargando…

FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei

BACKGROUND: The male germline in flowering plants differentiates by asymmetric division of haploid uninucleated microspores, giving rise to a vegetative cell enclosing a smaller generative cell, which eventually undergoes a second mitosis to originate two sperm cells. The vegetative cell and the spe...

Descripción completa

Detalles Bibliográficos
Autores principales: Borges, Filipe, Gardner, Rui, Lopes, Telma, Calarco, Joseph P, Boavida, Leonor C, Slotkin, R Keith, Martienssen, Robert A, Becker, Jörg D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502443/
https://www.ncbi.nlm.nih.gov/pubmed/23075219
http://dx.doi.org/10.1186/1746-4811-8-44
_version_ 1782250339984998400
author Borges, Filipe
Gardner, Rui
Lopes, Telma
Calarco, Joseph P
Boavida, Leonor C
Slotkin, R Keith
Martienssen, Robert A
Becker, Jörg D
author_facet Borges, Filipe
Gardner, Rui
Lopes, Telma
Calarco, Joseph P
Boavida, Leonor C
Slotkin, R Keith
Martienssen, Robert A
Becker, Jörg D
author_sort Borges, Filipe
collection PubMed
description BACKGROUND: The male germline in flowering plants differentiates by asymmetric division of haploid uninucleated microspores, giving rise to a vegetative cell enclosing a smaller generative cell, which eventually undergoes a second mitosis to originate two sperm cells. The vegetative cell and the sperm cells activate distinct genetic and epigenetic mechanisms to control pollen tube growth and germ cell specification, respectively. Therefore, a comprehensive characterization of these processes relies on efficient methods to isolate each of the different cell types throughout male gametogenesis. RESULTS: We developed stable transgenic Arabidopsis lines and reliable purification tools based on Fluorescence-Activated Cell Sorting (FACS) in order to isolate highly pure and viable fractions of each cell/nuclei type before and after pollen mitosis. In the case of mature pollen, this was accomplished by expressing GFP and RFP in the sperm and vegetative nuclei, respectively, resulting in 99% pure sorted populations. Microspores were also purified by FACS taking advantage of their characteristic small size and autofluorescent properties, and were confirmed to be 98% pure. CONCLUSIONS: We provide simple and efficient FACS-based purification protocols for Arabidopsis microspores, vegetative nuclei and sperm cells. This paves the way for subsequent molecular analysis such as transcriptomics, DNA methylation analysis and chromatin immunoprecipitation, in the developmental context of microgametogenesis in Arabidopsis.
format Online
Article
Text
id pubmed-3502443
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-35024432012-11-21 FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei Borges, Filipe Gardner, Rui Lopes, Telma Calarco, Joseph P Boavida, Leonor C Slotkin, R Keith Martienssen, Robert A Becker, Jörg D Plant Methods Methodology BACKGROUND: The male germline in flowering plants differentiates by asymmetric division of haploid uninucleated microspores, giving rise to a vegetative cell enclosing a smaller generative cell, which eventually undergoes a second mitosis to originate two sperm cells. The vegetative cell and the sperm cells activate distinct genetic and epigenetic mechanisms to control pollen tube growth and germ cell specification, respectively. Therefore, a comprehensive characterization of these processes relies on efficient methods to isolate each of the different cell types throughout male gametogenesis. RESULTS: We developed stable transgenic Arabidopsis lines and reliable purification tools based on Fluorescence-Activated Cell Sorting (FACS) in order to isolate highly pure and viable fractions of each cell/nuclei type before and after pollen mitosis. In the case of mature pollen, this was accomplished by expressing GFP and RFP in the sperm and vegetative nuclei, respectively, resulting in 99% pure sorted populations. Microspores were also purified by FACS taking advantage of their characteristic small size and autofluorescent properties, and were confirmed to be 98% pure. CONCLUSIONS: We provide simple and efficient FACS-based purification protocols for Arabidopsis microspores, vegetative nuclei and sperm cells. This paves the way for subsequent molecular analysis such as transcriptomics, DNA methylation analysis and chromatin immunoprecipitation, in the developmental context of microgametogenesis in Arabidopsis. BioMed Central 2012-10-17 /pmc/articles/PMC3502443/ /pubmed/23075219 http://dx.doi.org/10.1186/1746-4811-8-44 Text en Copyright ©2012 Borges et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Borges, Filipe
Gardner, Rui
Lopes, Telma
Calarco, Joseph P
Boavida, Leonor C
Slotkin, R Keith
Martienssen, Robert A
Becker, Jörg D
FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei
title FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei
title_full FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei
title_fullStr FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei
title_full_unstemmed FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei
title_short FACS-based purification of Arabidopsis microspores, sperm cells and vegetative nuclei
title_sort facs-based purification of arabidopsis microspores, sperm cells and vegetative nuclei
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502443/
https://www.ncbi.nlm.nih.gov/pubmed/23075219
http://dx.doi.org/10.1186/1746-4811-8-44
work_keys_str_mv AT borgesfilipe facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT gardnerrui facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT lopestelma facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT calarcojosephp facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT boavidaleonorc facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT slotkinrkeith facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT martienssenroberta facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei
AT beckerjorgd facsbasedpurificationofarabidopsismicrosporesspermcellsandvegetativenuclei