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SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development

Trithorax group (TrxG) proteins are evolutionarily conserved in eukaryotes and play critical roles in transcriptional activation via deposition of histone H3 lysine 4 trimethylation (H3K4me3) in chromatin. Several Arabidopsis TrxG members have been characterized, and among them SET DOMAIN GROUP 2 (S...

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Autores principales: Yao, Xiaozhen, Feng, Haiyang, Yu, Yu, Dong, Aiwu, Shen, Wen-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585709/
https://www.ncbi.nlm.nih.gov/pubmed/23483879
http://dx.doi.org/10.1371/journal.pone.0056537
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author Yao, Xiaozhen
Feng, Haiyang
Yu, Yu
Dong, Aiwu
Shen, Wen-Hui
author_facet Yao, Xiaozhen
Feng, Haiyang
Yu, Yu
Dong, Aiwu
Shen, Wen-Hui
author_sort Yao, Xiaozhen
collection PubMed
description Trithorax group (TrxG) proteins are evolutionarily conserved in eukaryotes and play critical roles in transcriptional activation via deposition of histone H3 lysine 4 trimethylation (H3K4me3) in chromatin. Several Arabidopsis TrxG members have been characterized, and among them SET DOMAIN GROUP 2 (SDG2) has been shown to be necessary for global genome-wide H3K4me3 deposition. Although pleiotropic phenotypes have been uncovered in the sdg2 mutants, SDG2 function in the regulation of stem cell activity has remained largely unclear. Here, we investigate the sdg2 mutant root phenotype and demonstrate that SDG2 is required for primary root stem cell niche (SCN) maintenance as well as for lateral root SCN establishment. Loss of SDG2 results in drastically reduced H3K4me3 levels in root SCN and differentiated cells and causes the loss of auxin gradient maximum in the root quiescent centre. Elevated DNA damage is detected in the sdg2 mutant, suggesting that impaired genome integrity may also have challenged the stem cell activity. Genetic interaction analysis reveals that SDG2 and CHROMATIN ASSEMBLY FACTOR-1 act synergistically in root SCN and genome integrity maintenance but not in telomere length maintenance. We conclude that SDG2-mediated H3K4me3 plays a distinctive role in the regulation of chromatin structure and genome integrity, which are key features in pluripotency of stem cells and crucial for root growth and development.
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spelling pubmed-35857092013-03-12 SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development Yao, Xiaozhen Feng, Haiyang Yu, Yu Dong, Aiwu Shen, Wen-Hui PLoS One Research Article Trithorax group (TrxG) proteins are evolutionarily conserved in eukaryotes and play critical roles in transcriptional activation via deposition of histone H3 lysine 4 trimethylation (H3K4me3) in chromatin. Several Arabidopsis TrxG members have been characterized, and among them SET DOMAIN GROUP 2 (SDG2) has been shown to be necessary for global genome-wide H3K4me3 deposition. Although pleiotropic phenotypes have been uncovered in the sdg2 mutants, SDG2 function in the regulation of stem cell activity has remained largely unclear. Here, we investigate the sdg2 mutant root phenotype and demonstrate that SDG2 is required for primary root stem cell niche (SCN) maintenance as well as for lateral root SCN establishment. Loss of SDG2 results in drastically reduced H3K4me3 levels in root SCN and differentiated cells and causes the loss of auxin gradient maximum in the root quiescent centre. Elevated DNA damage is detected in the sdg2 mutant, suggesting that impaired genome integrity may also have challenged the stem cell activity. Genetic interaction analysis reveals that SDG2 and CHROMATIN ASSEMBLY FACTOR-1 act synergistically in root SCN and genome integrity maintenance but not in telomere length maintenance. We conclude that SDG2-mediated H3K4me3 plays a distinctive role in the regulation of chromatin structure and genome integrity, which are key features in pluripotency of stem cells and crucial for root growth and development. Public Library of Science 2013-02-19 /pmc/articles/PMC3585709/ /pubmed/23483879 http://dx.doi.org/10.1371/journal.pone.0056537 Text en © 2013 Yao 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
Yao, Xiaozhen
Feng, Haiyang
Yu, Yu
Dong, Aiwu
Shen, Wen-Hui
SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development
title SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development
title_full SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development
title_fullStr SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development
title_full_unstemmed SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development
title_short SDG2-Mediated H3K4 Methylation Is Required for Proper Arabidopsis Root Growth and Development
title_sort sdg2-mediated h3k4 methylation is required for proper arabidopsis root growth and development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585709/
https://www.ncbi.nlm.nih.gov/pubmed/23483879
http://dx.doi.org/10.1371/journal.pone.0056537
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