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Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize

Transcriptional gene silencing is a gene regulatory mechanism essential to all organisms. Many transcriptional regulatory mechanisms are associated with epigenetic modifications such as changes in chromatin structure, acetylation and methylation of core histone proteins, and DNA methylation within r...

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Autores principales: Madzima, Thelma F., Mills, E. Shannon, Gardiner, Jack M., McGinnis, Karen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276119/
https://www.ncbi.nlm.nih.gov/pubmed/22384320
http://dx.doi.org/10.1534/g3.111.000232
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author Madzima, Thelma F.
Mills, E. Shannon
Gardiner, Jack M.
McGinnis, Karen M.
author_facet Madzima, Thelma F.
Mills, E. Shannon
Gardiner, Jack M.
McGinnis, Karen M.
author_sort Madzima, Thelma F.
collection PubMed
description Transcriptional gene silencing is a gene regulatory mechanism essential to all organisms. Many transcriptional regulatory mechanisms are associated with epigenetic modifications such as changes in chromatin structure, acetylation and methylation of core histone proteins, and DNA methylation within regulatory regions of endogenous genes and transgenes. Although several maize mutants have been identified from prior forward genetic screens for epigenetic transcriptional silencing, these screens have been far from saturated. Herein, the transcriptionally silent b1 genomic transgene (BTG-silent), a stable, epigenetically silenced transgene in Zea mays (maize), is demonstrated to be an effective phenotype for a forward genetic screen. When the transgene is reactivated, a dark purple plant phenotype is evident because the B1 transcription factor activates anthocyanin biosynthesis, making loss of silencing mutants easy to identify. Using BTG-silent, ten new putative mutants were identified and named transgene reactivated1 through 11 (tgr1-6 and tgr8-11). Three of these mutants have been examined in more detail, and molecular and genetic assays demonstrated that these mutants have both distinct and overlapping phenotypes with previously identified maize mutants that relieve epigenetic transcriptional silencing. Linkage analysis suggests that tgr2 and tgr3 do not correspond to a mutation at previously identified maize loci resulting from other forward genetic screens, while tgr1 shows linkage to a characterized gene. These results suggest that the mutants are a valuable resource for future studies because some of the mutants are likely to reveal genes that encode products required for epigenetic gene regulation in maize but are not currently represented by sequenced mutations.
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spelling pubmed-32761192012-03-01 Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize Madzima, Thelma F. Mills, E. Shannon Gardiner, Jack M. McGinnis, Karen M. G3 (Bethesda) Investigation Transcriptional gene silencing is a gene regulatory mechanism essential to all organisms. Many transcriptional regulatory mechanisms are associated with epigenetic modifications such as changes in chromatin structure, acetylation and methylation of core histone proteins, and DNA methylation within regulatory regions of endogenous genes and transgenes. Although several maize mutants have been identified from prior forward genetic screens for epigenetic transcriptional silencing, these screens have been far from saturated. Herein, the transcriptionally silent b1 genomic transgene (BTG-silent), a stable, epigenetically silenced transgene in Zea mays (maize), is demonstrated to be an effective phenotype for a forward genetic screen. When the transgene is reactivated, a dark purple plant phenotype is evident because the B1 transcription factor activates anthocyanin biosynthesis, making loss of silencing mutants easy to identify. Using BTG-silent, ten new putative mutants were identified and named transgene reactivated1 through 11 (tgr1-6 and tgr8-11). Three of these mutants have been examined in more detail, and molecular and genetic assays demonstrated that these mutants have both distinct and overlapping phenotypes with previously identified maize mutants that relieve epigenetic transcriptional silencing. Linkage analysis suggests that tgr2 and tgr3 do not correspond to a mutation at previously identified maize loci resulting from other forward genetic screens, while tgr1 shows linkage to a characterized gene. These results suggest that the mutants are a valuable resource for future studies because some of the mutants are likely to reveal genes that encode products required for epigenetic gene regulation in maize but are not currently represented by sequenced mutations. Genetics Society of America 2011-06-01 /pmc/articles/PMC3276119/ /pubmed/22384320 http://dx.doi.org/10.1534/g3.111.000232 Text en Copyright © 2011 Madzima et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Madzima, Thelma F.
Mills, E. Shannon
Gardiner, Jack M.
McGinnis, Karen M.
Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize
title Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize
title_full Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize
title_fullStr Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize
title_full_unstemmed Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize
title_short Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize
title_sort identification of epigenetic regulators of a transcriptionally silenced transgene in maize
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276119/
https://www.ncbi.nlm.nih.gov/pubmed/22384320
http://dx.doi.org/10.1534/g3.111.000232
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