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Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)

Members of the Cyperaceae family exhibit an asymmetric microsporogenesis that results in the degeneration of three out of four meiotic products. Efforts have been made previously to describe the resulting structure, named the pseudomonad, but mechanisms concerning the establishment of cell domains,...

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Autores principales: Rocha, Danilo M., Marques, André, Andrade, Celia G.T.J., Guyot, Romain, Chaluvadi, Srinivasa R., Pedrosa-Harand, Andrea, Houben, Andreas, Bennetzen, Jeffrey L., Vanzela, André L.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049389/
https://www.ncbi.nlm.nih.gov/pubmed/27492982
http://dx.doi.org/10.1093/jxb/erw300
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author Rocha, Danilo M.
Marques, André
Andrade, Celia G.T.J.
Guyot, Romain
Chaluvadi, Srinivasa R.
Pedrosa-Harand, Andrea
Houben, Andreas
Bennetzen, Jeffrey L.
Vanzela, André L.L.
author_facet Rocha, Danilo M.
Marques, André
Andrade, Celia G.T.J.
Guyot, Romain
Chaluvadi, Srinivasa R.
Pedrosa-Harand, Andrea
Houben, Andreas
Bennetzen, Jeffrey L.
Vanzela, André L.L.
author_sort Rocha, Danilo M.
collection PubMed
description Members of the Cyperaceae family exhibit an asymmetric microsporogenesis that results in the degeneration of three out of four meiotic products. Efforts have been made previously to describe the resulting structure, named the pseudomonad, but mechanisms concerning the establishment of cell domains, nuclear development, and programmed cell death are largely unknown. Using the Rhynchospora genus as a model, evidence for cell asymmetry, cytoplasmic isolation, and programmed cell death was obtained by a combination of electron microscopic, cytochemical, immunocytochemical, in situ hybridization, and flow cytometric methods. Degenerative cells were identified at the abaxial region, with the cytoskeleton marking their delimitation from the functional domain after meiosis. After attempting to initiate cell division with an unreplicated genome and abnormal spindle assembly, these cells exhibited a gradual process of cytoplasmic contraction associated with hypermethylation of cytosines and differential loss of DNA. These results indicate that the asymmetric tetrad establishes a functional cell, where one nucleus is preferentially selected to survive. Degenerative haploid cells are then eliminated in a multistep process associated with mitotic disorder, non-random elimination of repetitive DNA, vacuolar cell death, and DNA fragmentation.
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spelling pubmed-50493892016-10-05 Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae) Rocha, Danilo M. Marques, André Andrade, Celia G.T.J. Guyot, Romain Chaluvadi, Srinivasa R. Pedrosa-Harand, Andrea Houben, Andreas Bennetzen, Jeffrey L. Vanzela, André L.L. J Exp Bot Research Paper Members of the Cyperaceae family exhibit an asymmetric microsporogenesis that results in the degeneration of three out of four meiotic products. Efforts have been made previously to describe the resulting structure, named the pseudomonad, but mechanisms concerning the establishment of cell domains, nuclear development, and programmed cell death are largely unknown. Using the Rhynchospora genus as a model, evidence for cell asymmetry, cytoplasmic isolation, and programmed cell death was obtained by a combination of electron microscopic, cytochemical, immunocytochemical, in situ hybridization, and flow cytometric methods. Degenerative cells were identified at the abaxial region, with the cytoskeleton marking their delimitation from the functional domain after meiosis. After attempting to initiate cell division with an unreplicated genome and abnormal spindle assembly, these cells exhibited a gradual process of cytoplasmic contraction associated with hypermethylation of cytosines and differential loss of DNA. These results indicate that the asymmetric tetrad establishes a functional cell, where one nucleus is preferentially selected to survive. Degenerative haploid cells are then eliminated in a multistep process associated with mitotic disorder, non-random elimination of repetitive DNA, vacuolar cell death, and DNA fragmentation. Oxford University Press 2016-10 2016-08-04 /pmc/articles/PMC5049389/ /pubmed/27492982 http://dx.doi.org/10.1093/jxb/erw300 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Rocha, Danilo M.
Marques, André
Andrade, Celia G.T.J.
Guyot, Romain
Chaluvadi, Srinivasa R.
Pedrosa-Harand, Andrea
Houben, Andreas
Bennetzen, Jeffrey L.
Vanzela, André L.L.
Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)
title Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)
title_full Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)
title_fullStr Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)
title_full_unstemmed Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)
title_short Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae)
title_sort developmental programmed cell death during asymmetric microsporogenesis in holocentric species of rhynchospora (cyperaceae)
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049389/
https://www.ncbi.nlm.nih.gov/pubmed/27492982
http://dx.doi.org/10.1093/jxb/erw300
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