Evidence map›Paper›PMID 36199058›Full record

ArticleBMC biology2022

Activation function 1 of progesterone receptor is required for progesterone antagonism of oestrogen action in the uterus.

Shi Hao Lee, Chew Leng Lim, Wei Shen, Samuel Ming Xuan Tan, Amanda Rui En Woo, Yeannie H Y Yap, Caitlyn Ang Su Sian, Wilson Wen Bin Goh, Wei-Ping Yu, Li Li and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMC biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 3 countries.

Shi Hao Lee *School of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Chew Leng Lim *School of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Wei ShenCollege of Informatics, Huazhong Agricultural University, Wuhan, China.
Samuel Ming Xuan TanSchool of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Amanda Rui En WooSchool of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Yeannie H Y YapSchool of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Caitlyn Ang Su SianSchool of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Wilson Wen Bin GohSchool of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
Wei-Ping YuAnimal Gene Editing Laboratory (AGEL), Biological Resource Centre, Agency for Science, Technology and Research (A*STAR), 61 Biopolis Drive, Proteos, Singapore, 138673, Singapore.
Li LiCollege of Informatics, Huazhong Agricultural University, Wuhan, China. li.li@mail.hzau.edu.cn.
Valerie C L LinSchool of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore. cllin@ntu.edu.sg.ORCID http://orcid.org/0000-0002-7997-2771
Nanyang Technological University · SGHuazhong Agricultural University · CNAgency for Science, Technology and Research · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProgesterone receptor (PGR) is a master regulator of uterine function through antagonistic and synergistic interplays with oestrogen receptors. PGR action is primarily mediated by activation functions AF1 and AF2, but their physiological significance is unknown.

resultsWe report the first study of AF1 function in mice. The AF1 mutant mice are infertile with impaired implantation and decidualization. This is associated with a delay in the cessation of epithelial proliferation and in the initiation of stromal proliferation at preimplantation. Despite tissue selective effect on PGR target genes, AF1 mutations caused global loss of the antioestrogenic activity of progesterone in both pregnant and ovariectomized models. Importantly, the study provides evidence that PGR can exert an antioestrogenic effect by genomic inhibition of Esr1 and Greb1 expression. ChIP-Seq data mining reveals intermingled PGR and ESR1 binding on Esr1 and Greb1 gene enhancers. Chromatin conformation analysis shows reduced interactions in these genes' loci in the mutant, coinciding with their upregulations.

conclusionAF1 mediates genomic inhibition of ESR1 action globally whilst it also has tissue-selective effect on PGR target genes.

Indexed as

ProgesteroneReceptors, ProgesteroneAnimalsChromatinEndometriumEstrogensFemaleFurylfuramideMicePregnancyReceptors, EstrogenUterusChromatinEstrogensFurylfuramideProgesteroneReceptors, EstrogenReceptors, ProgesteroneActivation function 1EndometriumESR1Genomic antagonismPGR

Identifiers

PMID36199058
PMCPMC9535881
OpenAlexW4302024690

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.