Cargando…

The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm

BACKGROUND: The silkworm, Bombyx mori, a typical representative of metamorphic insects, is of great agricultural and economic importance. The steroid hormone ecdysone (20-hydroxyecdysone, 20E) is the central regulator of insect developmental transitions, and its nuclear receptors are crucial for num...

Descripción completa

Detalles Bibliográficos
Autores principales: Cheng, Dong, Cheng, Tingcai, Yang, Xi, Zhang, Quan, Fu, Jianfeng, Feng, Tieshan, Gong, Jiao, Xia, Qingyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109983/
https://www.ncbi.nlm.nih.gov/pubmed/30149809
http://dx.doi.org/10.1186/s13072-018-0216-y
_version_ 1783350401600323584
author Cheng, Dong
Cheng, Tingcai
Yang, Xi
Zhang, Quan
Fu, Jianfeng
Feng, Tieshan
Gong, Jiao
Xia, Qingyou
author_facet Cheng, Dong
Cheng, Tingcai
Yang, Xi
Zhang, Quan
Fu, Jianfeng
Feng, Tieshan
Gong, Jiao
Xia, Qingyou
author_sort Cheng, Dong
collection PubMed
description BACKGROUND: The silkworm, Bombyx mori, a typical representative of metamorphic insects, is of great agricultural and economic importance. The steroid hormone ecdysone (20-hydroxyecdysone, 20E) is the central regulator of insect developmental transitions, and its nuclear receptors are crucial for numerous biological processes, including reproduction, metabolism, and immunity. However, genome-wide DNA regulatory elements and the ecdysone receptor (EcR) that control these programs of gene expression are not well defined. RESULTS: In this study, we investigated the alterations in three types of histone modification in silkworm embryonic cells treated with 20E by chromatin immunoprecipitation sequencing (ChIP-seq). We identified enhancers using histone modifications and derived genome-wide ecdysone-dependent enhancer activity maps in the silkworm. We found enhancers enriched for monomethylation of histone H3 Lys4 (H3K4me1) that showed dynamic changes in acetylation of histone H3 Lys27 (H3K27ac) after 20E treatment and functioned to regulate the transcription of specific genes. EcR regulated transcription by binding not only to proximal promoters but also to the distal enhancers of target genes. Moreover, only 52.65% EcR peaks contained ecdysone response element (EcRE) motif, suggesting that EcR regulates the expression of target genes not only by binding directly to EcRE, but also by binding with other transcription factor. CONCLUSIONS: Our findings provide novel insights into the complex regulatory landscape of hormone-responsive cell activity and a basis for understanding the complex transcriptional regulatory processes of ecdysone. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-018-0216-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6109983
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-61099832018-08-28 The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm Cheng, Dong Cheng, Tingcai Yang, Xi Zhang, Quan Fu, Jianfeng Feng, Tieshan Gong, Jiao Xia, Qingyou Epigenetics Chromatin Research BACKGROUND: The silkworm, Bombyx mori, a typical representative of metamorphic insects, is of great agricultural and economic importance. The steroid hormone ecdysone (20-hydroxyecdysone, 20E) is the central regulator of insect developmental transitions, and its nuclear receptors are crucial for numerous biological processes, including reproduction, metabolism, and immunity. However, genome-wide DNA regulatory elements and the ecdysone receptor (EcR) that control these programs of gene expression are not well defined. RESULTS: In this study, we investigated the alterations in three types of histone modification in silkworm embryonic cells treated with 20E by chromatin immunoprecipitation sequencing (ChIP-seq). We identified enhancers using histone modifications and derived genome-wide ecdysone-dependent enhancer activity maps in the silkworm. We found enhancers enriched for monomethylation of histone H3 Lys4 (H3K4me1) that showed dynamic changes in acetylation of histone H3 Lys27 (H3K27ac) after 20E treatment and functioned to regulate the transcription of specific genes. EcR regulated transcription by binding not only to proximal promoters but also to the distal enhancers of target genes. Moreover, only 52.65% EcR peaks contained ecdysone response element (EcRE) motif, suggesting that EcR regulates the expression of target genes not only by binding directly to EcRE, but also by binding with other transcription factor. CONCLUSIONS: Our findings provide novel insights into the complex regulatory landscape of hormone-responsive cell activity and a basis for understanding the complex transcriptional regulatory processes of ecdysone. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-018-0216-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-27 /pmc/articles/PMC6109983/ /pubmed/30149809 http://dx.doi.org/10.1186/s13072-018-0216-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Cheng, Dong
Cheng, Tingcai
Yang, Xi
Zhang, Quan
Fu, Jianfeng
Feng, Tieshan
Gong, Jiao
Xia, Qingyou
The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
title The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
title_full The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
title_fullStr The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
title_full_unstemmed The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
title_short The genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
title_sort genome-wide transcriptional regulatory landscape of ecdysone in the silkworm
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109983/
https://www.ncbi.nlm.nih.gov/pubmed/30149809
http://dx.doi.org/10.1186/s13072-018-0216-y
work_keys_str_mv AT chengdong thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT chengtingcai thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT yangxi thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT zhangquan thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT fujianfeng thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT fengtieshan thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT gongjiao thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT xiaqingyou thegenomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT chengdong genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT chengtingcai genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT yangxi genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT zhangquan genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT fujianfeng genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT fengtieshan genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT gongjiao genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm
AT xiaqingyou genomewidetranscriptionalregulatorylandscapeofecdysoneinthesilkworm