Evidence map›Paper›PMID 33150487›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2021

Examining Sex Differences in the Human Placental Transcriptome During the First Fetal Androgen Peak.

Amy E Braun, Kristin L Muench, Beatriz G Robinson, Angela Wang, Theo D Palmer, Virginia D Winn

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 59 citations in OpenAlex.

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  15. Transcriptomic comparison of in vitro models of the human placenta.bioRxiv : the preprint server for biology · 2024
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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

6 authors at 2 institutions in 2 countries.

Amy E BraunDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, 300 Pasteur Dr. H333, Stanford, CA, 94305-5317, USA. amybraun@stanford.edu.ORCID 0000-0003-0480-1289
Kristin L MuenchInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, 265 Campus Drive, Rm 1141, Stanford, CA, 94305-5454, USA.
Beatriz G RobinsonInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, 265 Campus Drive, Rm 1141, Stanford, CA, 94305-5454, USA.
Angela WangDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, 300 Pasteur Dr. H333, Stanford, CA, 94305-5317, USA.
Theo D PalmerInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, 265 Campus Drive, Rm 1141, Stanford, CA, 94305-5454, USA.
Virginia D WinnDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, 300 Pasteur Dr. H333, Stanford, CA, 94305-5317, USA.
Stanford University · USCalifornia Institute for Regenerative Medicine · US

Funding

Training Program in Basic NeuroscienceT32MH020016 · NIMH · STANFORD UNIVERSITY · PI Justin L Gardner, Merritt C Maduke · 1997 to 2026
$16.2M
6 · The paper itself

Abstract

Sex differences in human placenta exist from early pregnancy to term, however, it is unclear whether these differences are driven solely by sex chromosome complement or are subject to differential sex hormonal regulation. Here, we survey the human chorionic villus (CV) transcriptome for sex-linked signatures from 11 to 16 gestational weeks, corresponding to the first window of increasing testis-derived androgen production in male fetuses. Illumina HiSeq RNA sequencing was performed on Lexogen Quantseq 3' libraries derived from CV biopsies (n = 11 females, n = 12 males). Differential expression (DE) was performed to identify sex-linked transcriptional signatures, followed by chromosome mapping, pathway analysis, predicted protein interaction, and post-hoc linear regressions to identify transcripts that trend over time. We observe 322 transcripts DE between male and female CV from 11 to 16 weeks, with 22 transcripts logFC > 1. Contrary to our predictions, the difference between male and female expression of DE autosomal genes was more pronounced at the earlier gestational ages. In females, we found selective upregulation of extracellular matrix components, along with a number of X-linked genes. In males, DE transcripts centered on chromosome 19, with mitochondrial, immune, and pregnancy maintenance-related transcripts upregulated. Among the highest differentially expressed autosomal genes were CCRL2, LGALS13, and LGALS14, which are known to regulate immune cell interactions. Our results provide insight into sex-linked gene expression in late first and early second trimester developing human placenta and lay the groundwork to understand the mechanistic origins of sex differences in prenatal development.

Indexed as

Gene Expression ProfilingSex Determination AnalysisTranscriptomeAndrogensChorionic VilliFemaleGalectinsGene Expression Regulation, DevelopmentalGene Regulatory NetworksGestational AgeHumansMalePregnancyPregnancy ProteinsReceptors, CCRSex Determination ProcessesAndrogensCCRL2 protein, humanGalectinsLGALS13 protein, humanPregnancy ProteinsReceptors, CCRChorionic villusFetal-maternal interfacePlacentaSex differencesTrancriptome

Identifiers

PMID33150487
OpenAlexW3097394238

What OpenQuestion holds

Textmetadata
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.