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CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana

BACKGROUND: The in vivo determination of the cell-specific chromosome number provides a valuable tool in several aspects of plant research. However, current techniques to determine the endosystemic ploidy level do not allow non-destructive, cell-specific chromosome quantification. Particularly in th...

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Autores principales: De Storme, Nico, Keçeli, Burcu Nur, Zamariola, Linda, Angenon, Geert, Geelen, Danny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700667/
https://www.ncbi.nlm.nih.gov/pubmed/26728271
http://dx.doi.org/10.1186/s12870-015-0700-5
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author De Storme, Nico
Keçeli, Burcu Nur
Zamariola, Linda
Angenon, Geert
Geelen, Danny
author_facet De Storme, Nico
Keçeli, Burcu Nur
Zamariola, Linda
Angenon, Geert
Geelen, Danny
author_sort De Storme, Nico
collection PubMed
description BACKGROUND: The in vivo determination of the cell-specific chromosome number provides a valuable tool in several aspects of plant research. However, current techniques to determine the endosystemic ploidy level do not allow non-destructive, cell-specific chromosome quantification. Particularly in the gametophytic cell lineages, which are physically encapsulated in the reproductive organ structures, direct in vivo ploidy determination has been proven very challenging. Using Arabidopsis thaliana as a model, we here assess the applicability of recombinant CENH3-GFP reporters for the labeling of the cell’s chromocenters and for the monitoring of the gametophytic and somatic chromosome number in vivo. RESULTS: By modulating expression of a CENH3-GFP reporter cassette using different promoters, we isolated two reporter lines that allow for a clear and highly specific labeling of centromeric chromosome regions in somatic and gametophytic cells respectively. Using polyploid plant series and reproductive mutants, we demonstrate that the pWOX2-CENH3-GFP recombinant fusion protein allows for the determination of the gametophytic chromosome number in both male and female gametophytic cells, and additionally labels centromeric regions in early embryo development. Somatic centromere labeling through p35S-CENH3-GFP shows a maximum of ten centromeric dots in young dividing tissues, reflecting the diploid chromosome number (2x = 10), and reveals a progressive decrease in GFP foci frequency throughout plant development. Moreover, using chemical and genetic induction of endomitosis, we demonstrate that CENH3-mediated chromosome labeling provides an easy and valuable tool for the detection and characterization of endomitotic polyploidization events. CONCLUSIONS: This study demonstrates that the introgression of the pWOX2-CENH3-GFP reporter construct in Arabidopsis thaliana provides an easy and reliable methodology for determining the chromosome number in developing male and female gametes, and during early embryo development. Somatically expressed CENH3-GFP reporters, on the other hand, constitute a valuable tool to quickly determine the basic somatic ploidy level in young seedlings at the individual cell level and to detect and to quantify endomitotic polyploidization events in a non-destructive, microscopy-based manner. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0700-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-47006672016-01-06 CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana De Storme, Nico Keçeli, Burcu Nur Zamariola, Linda Angenon, Geert Geelen, Danny BMC Plant Biol Methodology Article BACKGROUND: The in vivo determination of the cell-specific chromosome number provides a valuable tool in several aspects of plant research. However, current techniques to determine the endosystemic ploidy level do not allow non-destructive, cell-specific chromosome quantification. Particularly in the gametophytic cell lineages, which are physically encapsulated in the reproductive organ structures, direct in vivo ploidy determination has been proven very challenging. Using Arabidopsis thaliana as a model, we here assess the applicability of recombinant CENH3-GFP reporters for the labeling of the cell’s chromocenters and for the monitoring of the gametophytic and somatic chromosome number in vivo. RESULTS: By modulating expression of a CENH3-GFP reporter cassette using different promoters, we isolated two reporter lines that allow for a clear and highly specific labeling of centromeric chromosome regions in somatic and gametophytic cells respectively. Using polyploid plant series and reproductive mutants, we demonstrate that the pWOX2-CENH3-GFP recombinant fusion protein allows for the determination of the gametophytic chromosome number in both male and female gametophytic cells, and additionally labels centromeric regions in early embryo development. Somatic centromere labeling through p35S-CENH3-GFP shows a maximum of ten centromeric dots in young dividing tissues, reflecting the diploid chromosome number (2x = 10), and reveals a progressive decrease in GFP foci frequency throughout plant development. Moreover, using chemical and genetic induction of endomitosis, we demonstrate that CENH3-mediated chromosome labeling provides an easy and valuable tool for the detection and characterization of endomitotic polyploidization events. CONCLUSIONS: This study demonstrates that the introgression of the pWOX2-CENH3-GFP reporter construct in Arabidopsis thaliana provides an easy and reliable methodology for determining the chromosome number in developing male and female gametes, and during early embryo development. Somatically expressed CENH3-GFP reporters, on the other hand, constitute a valuable tool to quickly determine the basic somatic ploidy level in young seedlings at the individual cell level and to detect and to quantify endomitotic polyploidization events in a non-destructive, microscopy-based manner. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0700-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-05 /pmc/articles/PMC4700667/ /pubmed/26728271 http://dx.doi.org/10.1186/s12870-015-0700-5 Text en © De Storme et al. 2016 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 Article
De Storme, Nico
Keçeli, Burcu Nur
Zamariola, Linda
Angenon, Geert
Geelen, Danny
CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
title CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
title_full CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
title_fullStr CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
title_full_unstemmed CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
title_short CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana
title_sort cenh3-gfp: a visual marker for gametophytic and somatic ploidy determination in arabidopsis thaliana
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700667/
https://www.ncbi.nlm.nih.gov/pubmed/26728271
http://dx.doi.org/10.1186/s12870-015-0700-5
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