Evidence map›Paper›PMID 30149809›Full record

ArticleEpigenetics & chromatin2018

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

Dong Cheng, Tingcai Cheng, Xi Yang, Quan Zhang, Jianfeng Fu, Tieshan Feng, Jiao Gong, Qingyou Xia

Abstract read
In one paragraph

Article in Epigenetics & chromatin, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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  3. 20E-inducedProceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Dong ChengState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.
Tingcai ChengState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China. chengtc@swu.edu.cn.ORCID 0000-0002-3862-0817
Xi YangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.
Quan ZhangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.
Jianfeng FuState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.
Tieshan FengState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.
Jiao GongState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.
Qingyou XiaState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China.

Funding

Chongqing Research Program of Basic Research and Frontier Technology CSTC2018JCYJAX0396Fundamental Research Funds for the Central Universities XDJK2017C075National Natural Science Foundation of China 31372380
6 · The paper itself

Abstract

backgroundThe 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.

resultsIn 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.

conclusionsOur 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.

Indexed as

Histone CodeTranscriptomeAnimalsBombyxEcdysoneEnhancer Elements, GeneticInsect ProteinsReceptors, SteroidEcdysoneecdysone receptorInsect ProteinsReceptors, SteroidEcdysone receptorEnhancerHistone modificationRegulatory elementSilkworm

Identifiers

PMID30149809
PMCPMC6109983

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.