Evidence map›Paper›PMID 35150271›Full record

ArticleMolecular human reproduction2022

Transcriptomic analysis reveals myometrial topologically associated domains linked to the onset of human term labour.

Sonika Tyagi, Eng-Cheng Chan, Daniel Barker, Patrick McElduff, Kelly A Taylor, Carlos Riveros, Esha Singh, Roger Smith

Open access · hybridAbstract read
In one paragraph

Article in Molecular human reproduction, 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
0.7field-weighted citation impact, top 37% 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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Female Reproductive Systems: Hormone Dependence and Receptor Expression.Advances in experimental medicine and biology · 2022
    Article
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 3 institutions in 2 countries.

Sonika TyagiDepartment of Infectious Diseases, Central Clinical School, Monash University and the Alfred Hospital, Melbourne, VIC, Australia.ORCID 0000-0003-0181-6258
Eng-Cheng ChanMothers and Babies Research Centre, HMRI University of Newcastle, NSW, Australia.
Daniel BarkerUniversity of Newcastle, Newcastle, NSW, Australia.
Patrick McElduffUniversity of Newcastle, Newcastle, NSW, Australia.
Kelly A TaylorMothers and Babies Research Centre, HMRI University of Newcastle, NSW, Australia.
Carlos RiverosUniversity of Newcastle, Newcastle, NSW, Australia.
Esha SinghDepartment of Biotechnology and Biochemical Engineering, Indian Institute of Technology, New Delhi, India.
Roger SmithMothers and Babies Research Centre, HMRI University of Newcastle, NSW, Australia.ORCID 0000-0003-4720-0280
University of Newcastle Australia · AUDepartment of Biotechnology · INMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changes in cell phenotype are thought to occur through the expression of groups of co-regulated genes within topologically associated domains (TADs). In this paper, we allocate genes expressed within the myometrium of the human uterus during the onset of term labour into TADs. Transformation of the myometrial cells of the uterus into a contractile phenotype during term human labour is the result of a complex interaction of different epigenomic and genomic layers. Recent work suggests that the transcription factor (TF) RELA lies at the top of this regulatory network. Using deep RNA sequencing (RNAseq) analysis of myometrial samples (n = 16) obtained at term from women undergoing caesarean section prior to or after the onset of labour, we have identified evidence for how other gene expression regulatory elements interact with TFs in the labour phenotype transition. Gene set enrichment analysis of our RNAseq data identified three modules of enriched genes (M1, M2 and M3), which in gene ontology studies are linked to matrix degradation, smooth muscle and immune gene signatures, respectively. These genes were predominantly located within chromosomal TADs suggesting co-regulation of expression. Our transcriptomic analysis also identified significant differences in the expression of long non-coding RNAs (lncRNA), microRNAs (miRNA) and TFs that were predicted to target genes within the TADs. Additionally, network analysis revealed 15 new lncRNA (MCM3AP-AS1, TUG1, MIR29B2CHG, HCG18, LINC00963, KCNQ1OT1, NEAT1, HELLPAR, SNHG16, NUTM2B-AS1, MALAT1, PSMA3-AS1, GABPB1-AS1, NORAD and NKILA) and 4 miRNA (mir-145, mir-223, mir-let-7a and mir-132) as top gene hubs with three TFs (NFKB1, RELA and ESR1) as master regulators. Together, these factors are likely to be involved in co-regulatory networks driving a myometrial transformation to generate an estrogen-sensitive phenotype. We conclude that lncRNA and miRNA targeting the estrogen receptor 1 and nuclear factor kappa B pathways play a key role in the initiation of human labour. For the first time, we perform an integrative analysis to present a multi-level genomic signature made of mRNA, non-coding RNA and TFs in the myometrium for spontaneous term labour.

Indexed as

MicroRNAsRNA, Long NoncodingAcetyltransferasesCesarean SectionFemaleGene Regulatory NetworksHumansIntracellular Signaling Peptides and ProteinsMyometriumPregnancyTranscriptomeAcetyltransferasesIntracellular Signaling Peptides and ProteinsMCM3AP protein, humanMicroRNAsMIRN145 microRNA, humanRNA, Long Noncodingbioinformaticsepigenomeestrogenparturitionpregnancytopologically associated domains

Identifiers

PMID35150271
PMCPMC8903000
OpenAlexW4210841935

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.