Evidence map›Paper›PMID 30063711›Full record

ArticlePLoS biology2018

Maternal care boosted by paternal imprinting in mammals.

H D J Creeth, G I McNamara, S J Tunster, R Boque-Sastre, B Allen, L Sumption, J B Eddy, A R Isles, R M John

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Regulation of maternal-fetal metabolic communication.Cellular and molecular life sciences : CMLS · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

H D J CreethBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
G I McNamaraBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
S J TunsterBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
R Boque-SastreBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
B AllenBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
L SumptionBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
J B EddyBehavioural Genetics Group, MRC Centre for Neuropsychiatric Genetics and Genomics, Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom.
A R IslesBehavioural Genetics Group, MRC Centre for Neuropsychiatric Genetics and Genomics, Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom.
R M JohnBiomedicine Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.ORCID 0000-0002-3827-7617
Cardiff University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G015465/1Biotechnology and Biological Sciences Research Council BB/J015156Biotechnology and Biological Sciences Research Council BB/P002307Biotechnology and Biological Sciences Research Council BB/P008623Medical Research Council MR/L010305/1Medical Research Council MR/M013960/1
6 · The paper itself

Abstract

In mammals, mothers are the primary caregiver, programmed, in part, by hormones produced during pregnancy. High-quality maternal care is essential for the survival and lifelong health of offspring. We previously showed that the paternally silenced imprinted gene pleckstrin homology-like domain family A member 2 (Phlda2) functions to negatively regulate a single lineage in the mouse placenta called the spongiotrophoblast, a major source of hormones in pregnancy. Consequently, the offspring's Phlda2 gene dosage may influence the quality of care provided by the mother. Here, we show that wild-type (WT) female mice exposed to offspring with three different doses of the maternally expressed Phlda2 gene-two active alleles, one active allele (the extant state), and loss of function-show changes in the maternal hypothalamus and hippocampus during pregnancy, regions important for maternal-care behaviour. After birth, WT dams exposed in utero to offspring with the highest Phlda2 dose exhibit decreased nursing and grooming of pups and increased focus on nest building. Conversely, 'paternalised' dams, exposed to the lowest Phlda2 dose, showed increased nurturing of their pups, increased self-directed behaviour, and a decreased focus on nest building, behaviour that was robustly maintained in the absence of genetically modified pups. This work raises the intriguing possibility that imprinting of Phlda2 contributed to increased maternal care during the evolution of mammals.

Indexed as

Genomic ImprintingMaternal BehaviorAnimalsFemaleGene Expression Regulation, DevelopmentalHippocampusHypothalamusMaleMammalsMice, KnockoutNuclear ProteinsNuclear ProteinsTSSC3 protein

Identifiers

PMID30063711
PMCPMC6067684
OpenAlexW2887780846

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.