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Epigenomic Consequences of Immortalized Plant Cell Suspension Culture

Plant cells grown in culture exhibit genetic and epigenetic instability. Using a combination of chromatin immunoprecipitation and DNA methylation profiling on tiling microarrays, we have mapped the location and abundance of histone and DNA modifications in a continuously proliferating, dedifferentia...

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Autores principales: Tanurdzic, Milos, Vaughn, Matthew W, Jiang, Hongmei, Lee, Tae-Jin, Slotkin, R. Keith, Sosinski, Bryon, Thompson, William F, Doerge, R. W, Martienssen, Robert A
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596858/
https://www.ncbi.nlm.nih.gov/pubmed/19071958
http://dx.doi.org/10.1371/journal.pbio.0060302
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author Tanurdzic, Milos
Vaughn, Matthew W
Jiang, Hongmei
Lee, Tae-Jin
Slotkin, R. Keith
Sosinski, Bryon
Thompson, William F
Doerge, R. W
Martienssen, Robert A
author_facet Tanurdzic, Milos
Vaughn, Matthew W
Jiang, Hongmei
Lee, Tae-Jin
Slotkin, R. Keith
Sosinski, Bryon
Thompson, William F
Doerge, R. W
Martienssen, Robert A
author_sort Tanurdzic, Milos
collection PubMed
description Plant cells grown in culture exhibit genetic and epigenetic instability. Using a combination of chromatin immunoprecipitation and DNA methylation profiling on tiling microarrays, we have mapped the location and abundance of histone and DNA modifications in a continuously proliferating, dedifferentiated cell suspension culture of Arabidopsis. We have found that euchromatin becomes hypermethylated in culture and that a small percentage of the hypermethylated genes become associated with heterochromatic marks. In contrast, the heterochromatin undergoes dramatic and very precise DNA hypomethylation with transcriptional activation of specific transposable elements (TEs) in culture. High throughput sequencing of small interfering RNA (siRNA) revealed that TEs activated in culture have increased levels of 21-nucleotide (nt) siRNA, sometimes at the expense of the 24-nt siRNA class. In contrast, TEs that remain silent, which match the predominant 24-nt siRNA class, do not change significantly in their siRNA profiles. These results implicate RNA interference and chromatin modification in epigenetic restructuring of the genome following the activation of TEs in immortalized cell culture.
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spelling pubmed-25968582008-12-09 Epigenomic Consequences of Immortalized Plant Cell Suspension Culture Tanurdzic, Milos Vaughn, Matthew W Jiang, Hongmei Lee, Tae-Jin Slotkin, R. Keith Sosinski, Bryon Thompson, William F Doerge, R. W Martienssen, Robert A PLoS Biol Research Article Plant cells grown in culture exhibit genetic and epigenetic instability. Using a combination of chromatin immunoprecipitation and DNA methylation profiling on tiling microarrays, we have mapped the location and abundance of histone and DNA modifications in a continuously proliferating, dedifferentiated cell suspension culture of Arabidopsis. We have found that euchromatin becomes hypermethylated in culture and that a small percentage of the hypermethylated genes become associated with heterochromatic marks. In contrast, the heterochromatin undergoes dramatic and very precise DNA hypomethylation with transcriptional activation of specific transposable elements (TEs) in culture. High throughput sequencing of small interfering RNA (siRNA) revealed that TEs activated in culture have increased levels of 21-nucleotide (nt) siRNA, sometimes at the expense of the 24-nt siRNA class. In contrast, TEs that remain silent, which match the predominant 24-nt siRNA class, do not change significantly in their siRNA profiles. These results implicate RNA interference and chromatin modification in epigenetic restructuring of the genome following the activation of TEs in immortalized cell culture. Public Library of Science 2008-12 2008-12-09 /pmc/articles/PMC2596858/ /pubmed/19071958 http://dx.doi.org/10.1371/journal.pbio.0060302 Text en © 2008 Tanurdzic et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tanurdzic, Milos
Vaughn, Matthew W
Jiang, Hongmei
Lee, Tae-Jin
Slotkin, R. Keith
Sosinski, Bryon
Thompson, William F
Doerge, R. W
Martienssen, Robert A
Epigenomic Consequences of Immortalized Plant Cell Suspension Culture
title Epigenomic Consequences of Immortalized Plant Cell Suspension Culture
title_full Epigenomic Consequences of Immortalized Plant Cell Suspension Culture
title_fullStr Epigenomic Consequences of Immortalized Plant Cell Suspension Culture
title_full_unstemmed Epigenomic Consequences of Immortalized Plant Cell Suspension Culture
title_short Epigenomic Consequences of Immortalized Plant Cell Suspension Culture
title_sort epigenomic consequences of immortalized plant cell suspension culture
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596858/
https://www.ncbi.nlm.nih.gov/pubmed/19071958
http://dx.doi.org/10.1371/journal.pbio.0060302
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