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HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci
Cellular senescence is a stable cell growth arrest that is characterized by the silencing of proliferation-promoting genes through compaction of chromosomes into senescence-associated heterochromatin foci (SAHF). Paradoxically, senescence is also accompanied by increased transcription of certain gen...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100296/ https://www.ncbi.nlm.nih.gov/pubmed/27799366 http://dx.doi.org/10.1083/jcb.201608026 |
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author | Aird, Katherine M. Iwasaki, Osamu Kossenkov, Andrew V. Tanizawa, Hideki Fatkhutdinov, Nail Bitler, Benjamin G. Le, Linh Alicea, Gretchen Yang, Ting-Lin Johnson, F. Brad Noma, Ken-ichi Zhang, Rugang |
author_facet | Aird, Katherine M. Iwasaki, Osamu Kossenkov, Andrew V. Tanizawa, Hideki Fatkhutdinov, Nail Bitler, Benjamin G. Le, Linh Alicea, Gretchen Yang, Ting-Lin Johnson, F. Brad Noma, Ken-ichi Zhang, Rugang |
author_sort | Aird, Katherine M. |
collection | PubMed |
description | Cellular senescence is a stable cell growth arrest that is characterized by the silencing of proliferation-promoting genes through compaction of chromosomes into senescence-associated heterochromatin foci (SAHF). Paradoxically, senescence is also accompanied by increased transcription of certain genes encoding for secreted factors such as cytokines and chemokines, known as the senescence-associated secretory phenotype (SASP). How SASP genes are excluded from SAHF-mediated global gene silencing remains unclear. In this study, we report that high mobility group box 2 (HMGB2) orchestrates the chromatin landscape of SASP gene loci. HMGB2 preferentially localizes to SASP gene loci during senescence. Loss of HMGB2 during senescence blunts SASP gene expression by allowing for spreading of repressive heterochromatin into SASP gene loci. This correlates with incorporation of SASP gene loci into SAHF. Our results establish HMGB2 as a novel master regulator that orchestrates SASP through prevention of heterochromatin spreading to allow for exclusion of SASP gene loci from a global heterochromatin environment during senescence. |
format | Online Article Text |
id | pubmed-5100296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51002962017-05-07 HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci Aird, Katherine M. Iwasaki, Osamu Kossenkov, Andrew V. Tanizawa, Hideki Fatkhutdinov, Nail Bitler, Benjamin G. Le, Linh Alicea, Gretchen Yang, Ting-Lin Johnson, F. Brad Noma, Ken-ichi Zhang, Rugang J Cell Biol Research Articles Cellular senescence is a stable cell growth arrest that is characterized by the silencing of proliferation-promoting genes through compaction of chromosomes into senescence-associated heterochromatin foci (SAHF). Paradoxically, senescence is also accompanied by increased transcription of certain genes encoding for secreted factors such as cytokines and chemokines, known as the senescence-associated secretory phenotype (SASP). How SASP genes are excluded from SAHF-mediated global gene silencing remains unclear. In this study, we report that high mobility group box 2 (HMGB2) orchestrates the chromatin landscape of SASP gene loci. HMGB2 preferentially localizes to SASP gene loci during senescence. Loss of HMGB2 during senescence blunts SASP gene expression by allowing for spreading of repressive heterochromatin into SASP gene loci. This correlates with incorporation of SASP gene loci into SAHF. Our results establish HMGB2 as a novel master regulator that orchestrates SASP through prevention of heterochromatin spreading to allow for exclusion of SASP gene loci from a global heterochromatin environment during senescence. The Rockefeller University Press 2016-11-07 /pmc/articles/PMC5100296/ /pubmed/27799366 http://dx.doi.org/10.1083/jcb.201608026 Text en © 2016 Aird et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Aird, Katherine M. Iwasaki, Osamu Kossenkov, Andrew V. Tanizawa, Hideki Fatkhutdinov, Nail Bitler, Benjamin G. Le, Linh Alicea, Gretchen Yang, Ting-Lin Johnson, F. Brad Noma, Ken-ichi Zhang, Rugang HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
title | HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
title_full | HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
title_fullStr | HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
title_full_unstemmed | HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
title_short | HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
title_sort | hmgb2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100296/ https://www.ncbi.nlm.nih.gov/pubmed/27799366 http://dx.doi.org/10.1083/jcb.201608026 |
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