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Endoreplication and its consequences in the suspensor of Pisum sativum
KEY MESSAGE: DNA replication and continuous process of transcription during ongoing amitotic division accelerate the development of four-celled pea suspensor containing nuclei which create transient gradient of polyploidy necessary for correct embryo development. ABSTRACT: A suspensor, the link betw...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244982/ https://www.ncbi.nlm.nih.gov/pubmed/30132058 http://dx.doi.org/10.1007/s00299-018-2335-0 |
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author | Chmielnicka, Agnieszka Żabka, Aneta Winnicki, Konrad Maszewski, Janusz Polit, Justyna Teresa |
author_facet | Chmielnicka, Agnieszka Żabka, Aneta Winnicki, Konrad Maszewski, Janusz Polit, Justyna Teresa |
author_sort | Chmielnicka, Agnieszka |
collection | PubMed |
description | KEY MESSAGE: DNA replication and continuous process of transcription during ongoing amitotic division accelerate the development of four-celled pea suspensor containing nuclei which create transient gradient of polyploidy necessary for correct embryo development. ABSTRACT: A suspensor, the link between embryo proper and surrounding tissues, differs significantly in size, morphology, and degree of polyploidy among the species. The suspensor of Pisum sativum consists of four polynuclear cells (two hemispherical and two elongated) formed in two layers. Their nuclei undergo endoreplication reaching, respectively, up to 256C and 128–256C DNA levels in its hemispherical and elongated parts. Our study shows that endoreplication first appears in the spherical part of the suspensor, and, subsequently, in the elongated one. At the next stages of suspensor development, the increase in DNA content takes place also in a similar order. Thus, despite simple construction of the suspensor, its development, supported by endoreplication, creates a certain gradient of polyploidy, which occurs in more extensive suspensors. Moreover, the rapid development of suspensor is supported both by the initiation of DNA replication prior to the completion of amitotic division of its polyploidal nuclei and by a continuous process of transcription, which is silenced by chromatin condensation throughout mitosis. Furthermore, the increase in DNA content correlates with the greater amount of transcripts; however, the multiplication of DNA copies does not entail an increase (but fluctuation) in the mean transcriptional activity of a particular nucleus during the next stages of suspensor development. |
format | Online Article Text |
id | pubmed-6244982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-62449822018-12-04 Endoreplication and its consequences in the suspensor of Pisum sativum Chmielnicka, Agnieszka Żabka, Aneta Winnicki, Konrad Maszewski, Janusz Polit, Justyna Teresa Plant Cell Rep Original Article KEY MESSAGE: DNA replication and continuous process of transcription during ongoing amitotic division accelerate the development of four-celled pea suspensor containing nuclei which create transient gradient of polyploidy necessary for correct embryo development. ABSTRACT: A suspensor, the link between embryo proper and surrounding tissues, differs significantly in size, morphology, and degree of polyploidy among the species. The suspensor of Pisum sativum consists of four polynuclear cells (two hemispherical and two elongated) formed in two layers. Their nuclei undergo endoreplication reaching, respectively, up to 256C and 128–256C DNA levels in its hemispherical and elongated parts. Our study shows that endoreplication first appears in the spherical part of the suspensor, and, subsequently, in the elongated one. At the next stages of suspensor development, the increase in DNA content takes place also in a similar order. Thus, despite simple construction of the suspensor, its development, supported by endoreplication, creates a certain gradient of polyploidy, which occurs in more extensive suspensors. Moreover, the rapid development of suspensor is supported both by the initiation of DNA replication prior to the completion of amitotic division of its polyploidal nuclei and by a continuous process of transcription, which is silenced by chromatin condensation throughout mitosis. Furthermore, the increase in DNA content correlates with the greater amount of transcripts; however, the multiplication of DNA copies does not entail an increase (but fluctuation) in the mean transcriptional activity of a particular nucleus during the next stages of suspensor development. Springer Berlin Heidelberg 2018-08-21 2018 /pmc/articles/PMC6244982/ /pubmed/30132058 http://dx.doi.org/10.1007/s00299-018-2335-0 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. |
spellingShingle | Original Article Chmielnicka, Agnieszka Żabka, Aneta Winnicki, Konrad Maszewski, Janusz Polit, Justyna Teresa Endoreplication and its consequences in the suspensor of Pisum sativum |
title | Endoreplication and its consequences in the suspensor of Pisum sativum |
title_full | Endoreplication and its consequences in the suspensor of Pisum sativum |
title_fullStr | Endoreplication and its consequences in the suspensor of Pisum sativum |
title_full_unstemmed | Endoreplication and its consequences in the suspensor of Pisum sativum |
title_short | Endoreplication and its consequences in the suspensor of Pisum sativum |
title_sort | endoreplication and its consequences in the suspensor of pisum sativum |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244982/ https://www.ncbi.nlm.nih.gov/pubmed/30132058 http://dx.doi.org/10.1007/s00299-018-2335-0 |
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