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Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis

Despite the well-established role of heterochromatin in protecting chromosomal integrity during meiosis and mitosis, the contribution and extent of heterochromatic histone posttranslational modifications (PTMs) remain poorly defined. Here, we gained novel functional insight about heterochromatic PTM...

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Autores principales: Papazyan, Romeo, Voronina, Ekaterina, Chapman, Jessica R, Luperchio, Teresa R, Gilbert, Tonya M, Meier, Elizabeth, Mackintosh, Samuel G, Shabanowitz, Jeffrey, Tackett, Alan J, Reddy, Karen L, Coyne, Robert S, Hunt, Donald F, Liu, Yifan, Taverna, Sean D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141274/
https://www.ncbi.nlm.nih.gov/pubmed/25161194
http://dx.doi.org/10.7554/eLife.02996
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author Papazyan, Romeo
Voronina, Ekaterina
Chapman, Jessica R
Luperchio, Teresa R
Gilbert, Tonya M
Meier, Elizabeth
Mackintosh, Samuel G
Shabanowitz, Jeffrey
Tackett, Alan J
Reddy, Karen L
Coyne, Robert S
Hunt, Donald F
Liu, Yifan
Taverna, Sean D
author_facet Papazyan, Romeo
Voronina, Ekaterina
Chapman, Jessica R
Luperchio, Teresa R
Gilbert, Tonya M
Meier, Elizabeth
Mackintosh, Samuel G
Shabanowitz, Jeffrey
Tackett, Alan J
Reddy, Karen L
Coyne, Robert S
Hunt, Donald F
Liu, Yifan
Taverna, Sean D
author_sort Papazyan, Romeo
collection PubMed
description Despite the well-established role of heterochromatin in protecting chromosomal integrity during meiosis and mitosis, the contribution and extent of heterochromatic histone posttranslational modifications (PTMs) remain poorly defined. Here, we gained novel functional insight about heterochromatic PTMs by analyzing histone H3 purified from the heterochromatic germline micronucleus of the model organism Tetrahymena thermophila. Mass spectrometric sequencing of micronuclear H3 identified H3K23 trimethylation (H3K23me3), a previously uncharacterized PTM. H3K23me3 became particularly enriched during meiotic leptotene and zygotene in germline chromatin of Tetrahymena and C. elegans. Loss of H3K23me3 in Tetrahymena through deletion of the methyltransferase Ezl3p caused mislocalization of meiosis-induced DNA double-strand breaks (DSBs) to heterochromatin, and a decrease in progeny viability. These results show that an evolutionarily conserved developmental pathway regulates H3K23me3 during meiosis, and our studies in Tetrahymena suggest this pathway may function to protect heterochromatin from DSBs. DOI: http://dx.doi.org/10.7554/eLife.02996.001
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spelling pubmed-41412742014-08-27 Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis Papazyan, Romeo Voronina, Ekaterina Chapman, Jessica R Luperchio, Teresa R Gilbert, Tonya M Meier, Elizabeth Mackintosh, Samuel G Shabanowitz, Jeffrey Tackett, Alan J Reddy, Karen L Coyne, Robert S Hunt, Donald F Liu, Yifan Taverna, Sean D eLife Cell Biology Despite the well-established role of heterochromatin in protecting chromosomal integrity during meiosis and mitosis, the contribution and extent of heterochromatic histone posttranslational modifications (PTMs) remain poorly defined. Here, we gained novel functional insight about heterochromatic PTMs by analyzing histone H3 purified from the heterochromatic germline micronucleus of the model organism Tetrahymena thermophila. Mass spectrometric sequencing of micronuclear H3 identified H3K23 trimethylation (H3K23me3), a previously uncharacterized PTM. H3K23me3 became particularly enriched during meiotic leptotene and zygotene in germline chromatin of Tetrahymena and C. elegans. Loss of H3K23me3 in Tetrahymena through deletion of the methyltransferase Ezl3p caused mislocalization of meiosis-induced DNA double-strand breaks (DSBs) to heterochromatin, and a decrease in progeny viability. These results show that an evolutionarily conserved developmental pathway regulates H3K23me3 during meiosis, and our studies in Tetrahymena suggest this pathway may function to protect heterochromatin from DSBs. DOI: http://dx.doi.org/10.7554/eLife.02996.001 eLife Sciences Publications, Ltd 2014-08-26 /pmc/articles/PMC4141274/ /pubmed/25161194 http://dx.doi.org/10.7554/eLife.02996 Text en Copyright © 2014, Papazyan et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Papazyan, Romeo
Voronina, Ekaterina
Chapman, Jessica R
Luperchio, Teresa R
Gilbert, Tonya M
Meier, Elizabeth
Mackintosh, Samuel G
Shabanowitz, Jeffrey
Tackett, Alan J
Reddy, Karen L
Coyne, Robert S
Hunt, Donald F
Liu, Yifan
Taverna, Sean D
Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis
title Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis
title_full Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis
title_fullStr Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis
title_full_unstemmed Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis
title_short Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis
title_sort methylation of histone h3k23 blocks dna damage in pericentric heterochromatin during meiosis
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141274/
https://www.ncbi.nlm.nih.gov/pubmed/25161194
http://dx.doi.org/10.7554/eLife.02996
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