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Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites

Heterochromatin protein 1 (HP1) is an evolutionarily conserved protein across different eukaryotic species and is crucial for heterochromatin establishment and maintenance. The silkworm, Bombyx mori, encodes two HP1 proteins, BmHP1a and BmHP1b. In order to investigate the role of BmHP1a in transcrip...

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Autores principales: Shoji, Keisuke, Hara, Kahori, Kawamoto, Munetaka, Kiuchi, Takashi, Kawaoka, Shinpei, Sugano, Sumio, Shimada, Toru, Suzuki, Yutaka, Katsuma, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191426/
https://www.ncbi.nlm.nih.gov/pubmed/25237056
http://dx.doi.org/10.1093/nar/gku862
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author Shoji, Keisuke
Hara, Kahori
Kawamoto, Munetaka
Kiuchi, Takashi
Kawaoka, Shinpei
Sugano, Sumio
Shimada, Toru
Suzuki, Yutaka
Katsuma, Susumu
author_facet Shoji, Keisuke
Hara, Kahori
Kawamoto, Munetaka
Kiuchi, Takashi
Kawaoka, Shinpei
Sugano, Sumio
Shimada, Toru
Suzuki, Yutaka
Katsuma, Susumu
author_sort Shoji, Keisuke
collection PubMed
description Heterochromatin protein 1 (HP1) is an evolutionarily conserved protein across different eukaryotic species and is crucial for heterochromatin establishment and maintenance. The silkworm, Bombyx mori, encodes two HP1 proteins, BmHP1a and BmHP1b. In order to investigate the role of BmHP1a in transcriptional regulation, we performed genome-wide analyses of the transcriptome, transcription start sites (TSSs), chromatin modification states and BmHP1a-binding sites of the silkworm ovary-derived BmN4 cell line. We identified a number of BmHP1a-binding loci throughout the silkworm genome and found that these loci included TSSs and frequently co-occurred with neighboring euchromatic histone modifications. In addition, we observed that genes with BmHP1a-associated TSSs were relatively highly expressed in BmN4 cells. RNA interference-mediated BmHP1a depletion resulted in the transcriptional repression of highly expressed genes with BmHP1a-associated TSSs, whereas genes not coupled with BmHP1a-binding regions were less affected by the treatment. These results demonstrate that BmHP1a binds near TSSs of highly expressed euchromatic genes and positively regulates their expression. Our study revealed a novel mode of transcriptional regulation mediated by HP1 proteins.
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spelling pubmed-41914262015-04-02 Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites Shoji, Keisuke Hara, Kahori Kawamoto, Munetaka Kiuchi, Takashi Kawaoka, Shinpei Sugano, Sumio Shimada, Toru Suzuki, Yutaka Katsuma, Susumu Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Heterochromatin protein 1 (HP1) is an evolutionarily conserved protein across different eukaryotic species and is crucial for heterochromatin establishment and maintenance. The silkworm, Bombyx mori, encodes two HP1 proteins, BmHP1a and BmHP1b. In order to investigate the role of BmHP1a in transcriptional regulation, we performed genome-wide analyses of the transcriptome, transcription start sites (TSSs), chromatin modification states and BmHP1a-binding sites of the silkworm ovary-derived BmN4 cell line. We identified a number of BmHP1a-binding loci throughout the silkworm genome and found that these loci included TSSs and frequently co-occurred with neighboring euchromatic histone modifications. In addition, we observed that genes with BmHP1a-associated TSSs were relatively highly expressed in BmN4 cells. RNA interference-mediated BmHP1a depletion resulted in the transcriptional repression of highly expressed genes with BmHP1a-associated TSSs, whereas genes not coupled with BmHP1a-binding regions were less affected by the treatment. These results demonstrate that BmHP1a binds near TSSs of highly expressed euchromatic genes and positively regulates their expression. Our study revealed a novel mode of transcriptional regulation mediated by HP1 proteins. Oxford University Press 2014-10-13 2014-09-18 /pmc/articles/PMC4191426/ /pubmed/25237056 http://dx.doi.org/10.1093/nar/gku862 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Shoji, Keisuke
Hara, Kahori
Kawamoto, Munetaka
Kiuchi, Takashi
Kawaoka, Shinpei
Sugano, Sumio
Shimada, Toru
Suzuki, Yutaka
Katsuma, Susumu
Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
title Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
title_full Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
title_fullStr Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
title_full_unstemmed Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
title_short Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
title_sort silkworm hp1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191426/
https://www.ncbi.nlm.nih.gov/pubmed/25237056
http://dx.doi.org/10.1093/nar/gku862
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