Evidence map›Paper›PMID 35685458›Full record

ArticleGenes & diseases2022

BET bromodomain inhibitor JQ1 regulates spermatid development by changing chromatin conformation in mouse spermatogenesis.

Xiaorong Wang, Mengmeng Sang, Shengnan Gong, Zhichuan Chen, Xi Zhao, Guishuan Wang, Zhiran Li, Yingying Huang, Shitao Chen, Gangcai Xie and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & diseases, 2022. 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
0.2field-weighted citation impact, top 49% 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, 6 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

12 authors at 3 institutions in 1 country.

Xiaorong WangInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Mengmeng SangInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Shengnan GongInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Zhichuan ChenInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Xi ZhaoInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Guishuan WangInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Zhiran LiInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Yingying HuangInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Shitao ChenInternational Peace Maternity and Child Health Hospital, Shanghai Key Laboratory for Reproductive Medicine, School of Medicine, Shanghai Jiaotong University, Shanghai 200030, PR China.
Gangcai XieInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Enkui DuanState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, PR China.
Fei SunInstitute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
Nantong University · CNChinese Academy of Sciences · CNInternational Peace Maternity & Child Health Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a BET bromodomain inhibitor, JQ1 has been proven have efficacy against a number of different cancers. In terms of male reproduction, JQ1 may be used as a new type of contraceptive, since JQ1 treatment in male mice could lead to germ cell defects and a decrease of sperm motility, moreover, this effect is reversible. However, the mechanism of JQ1 acting on gene regulation in spermatogenesis remains unclear. Here, we performed single-cell RNA sequencing (scRNA-seq) on mouse testes treated with JQ1 or vehicle control to determine the transcriptional regulatory function of JQ1 in spermatogenesis at the single cell resolution. We confirmed that JQ1 treatment could increase the numbers of somatic cells and spermatocytes and decrease the numbers of spermatid cells. Gene Ontology (GO) analysis demonstrated that differentially expressed genes which were down-regulated after JQ1 injection were mainly enriched in "DNA conformation change" biological process in early developmental germ cells and "spermatid development" biological process in spermatid cells. ATAC-seq data further confirmed that JQ1 injection could change the open state of chromatin. In addition, JQ1 could change the numbers of accessible meiotic DNA double-stranded break sites and the types of transcription factor motif that functioned in pachytene spermatocytes and round spermatids. The multi-omics analysis revealed that JQ1 had the ability to regulate gene transcription by changing chromatin conformation in mouse spermatogenesis, which would potentiate the availability of JQ1 in male contraceptive.

Indexed as

Chromatin conformationJQ1scRNA-seqSpermatid developmentSpermatogenesis

Identifiers

PMID35685458
PMCPMC9170580
OpenAlexW3119865958

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.