Evidence map›Paper›PMID 25654229›Full record

ArticleInternational journal of molecular sciences2015

Ecdysone receptor (EcR) is involved in the transcription of cell cycle genes in the silkworm.

Wenliang Qian, Lixia Kang, Tianlei Zhang, Meng Meng, Yonghu Wang, Zhiqing Li, Qingyou Xia, Daojun Cheng

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 43% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 citing papers in PubMed, 4 citations in OpenAlex.

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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 at 1 institution in 1 country.

Wenliang QianState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. wenliang20081103@126.com.
Lixia KangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. hnklx1986@163.com.
Tianlei ZhangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. zhangtianlei2011@sina.com.
Meng MengState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. keven190@sina.com.
Yonghu WangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. wangyonghu2006@163.com.
Zhiqing LiState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. lizhiqing@swu.edu.cn.
Qingyou XiaState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. xiaqy@swu.edu.cn.
Daojun ChengState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China. chengdj@swu.edu.cn.
Southwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EcR (ecdysone receptor)-mediated ecdysone signaling pathway contributes to regulate the transcription of genes involved in various processes during insect development. In this work, we detected the expression of EcR gene in silkworm ovary-derived BmN4 cells and found that EcR RNAi result in an alteration of cell shape, indicating that EcR may orchestrate cell cycle progression. EcR RNAi and EcR overexpression analysis revealed that in the cultured BmN4 cells, EcR respectively promoted and suppressed the transcription of E2F-1 and CycE, two genes controlling cell cycle progression. Further examination demonstrated that ecdysone application in BmN4 cells not only changed the transcription of these two cell cycle genes like that under EcR overexpression, but also induced cell cycle arrest at G2/M phase. In vivo analysis confirmed that E2F-1 expression was elevated in silk gland of silkworm larvae after ecdysone application, which is same as its response to ecdysone in BmN4 cells. However, ecdysone also promotes CycE transcription in silk gland, and this is converse with the observation in BmN4 cells. These results provide new insights into understanding the roles of EcR-mediated ecdysone signaling in the regulation of cell cycle.

Indexed as

Gene Expression RegulationTranscription, GeneticAnimalsBombyxCell Cycle CheckpointsCell Cycle ProteinsCell LineDose-Response Relationship, DrugEcdysoneReceptors, SteroidRNA InterferenceCell Cycle ProteinsEcdysoneecdysone receptorReceptors, Steroid

Identifiers

PMID25654229
PMCPMC4346899
OpenAlexW1963679069

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.