Evidence map›Paper›PMID 22326222›Full record

ArticleCell metabolism2012

Imprinted gene dosage is critical for the transition to independent life.

Marika Charalambous, Sacramento R Ferron, Simao T da Rocha, Andrew J Murray, Timothy Rowland, Mitsuteru Ito, Karin Schuster-Gossler, Arturo Hernandez, Anne C Ferguson-Smith

Open access · hybridAbstract read
In one paragraph

Article in Cell metabolism, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. ImprintedeLife · 2023
    Article
  10. The imprinted gene Zac1 regulates steatosis in developmental cadmium-induced nonalcoholic fatty liver disease.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  11. Article
  12. Epigenetic control and genomic imprinting dynamics of the Dlk1-Dio3 domain.Frontiers in cell and developmental biology · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. The imprintedeLife · 2022
    Article
  17. Review
  18. Article
  19. Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  20. Genomic imprinting and its effects on postnatal growth and adult metabolism.Cellular and molecular life sciences : CMLS · 2019
    Review
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 3 institutions in 3 countries.

Marika CharalambousDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK. mc524@cam.ac.uk
Sacramento R Ferron
Simao T da Rocha
Andrew J Murray
Timothy Rowland
Mitsuteru Ito
Karin Schuster-Gossler
Arturo Hernandez
Anne C Ferguson-Smith
University of Cambridge · GBDartmouth College · USMedizinische Hochschule Hannover · DE

Funding

Transgenerational Epigenetic Programming of the Thyroid AxisR01DK095908 · NIDDK · MAINEHEALTH · PI Arturo Hernandez · 2012 to 2026
$5.1M
Epigenetic Influence on Thyroid Hormone Action in the Brain and on BehaviorR01MH096050 · NIMH · MAINEHEALTH · PI HERNANDEZ, ARTURO · 2012 to 2022
$3.9M
Medical Research Council MR/J001597/1NIDDK NIH HHS R01 DK095908NIMH NIH HHS R01 MH096050Wellcome Trust 095606
6 · The paper itself

Abstract

Neonatal survival in mammals is crucially dependent upon maintenance of body temperature. Neonatal body temperature is largely maintained by thermogenesis in brown adipose tissue (BAT). BAT develops perinatally in mice requiring integration of adipogenic and thermoregulatory gene pathways. We describe a regulatory mutation in the imprinted gene cluster on mouse chromosome 12 resulting in early postnatal lethality. Maternal inheritance of this mutation impairs the ability of young mice to maintain body temperature. While mechanisms of perinatal BAT development are well understood, our work highlights a second phase of BAT recruitment necessary to support small animals newly independent of the nest. We show that the imprinted delta-like homolog 1/preadipocyte factor (Dlk1/Pref1) and iodothyronine deiodinase type 3 (Dio3) functions converge on the development of brown fat at the transition to independent life. This shows that appropriate dosage control at imprinted loci can act as a critical determinant in postnatal survival during phases of physiological adaptation.

Indexed as

Adaptation, PhysiologicalAdipose Tissue, BrownAnimalsCalcium-Binding ProteinsDietEnzyme-Linked Immunosorbent AssayGene DosageGenomic ImprintingImmunohistochemistryIntercellular Signaling Peptides and ProteinsIodide PeroxidaseMiceMice, TransgenicMultigene FamilyMutationOxygen ConsumptionCalcium-Binding ProteinsDlk1 protein, mouseIntercellular Signaling Peptides and ProteinsIodide Peroxidaseiodothyronine deiodinase type III

Identifiers

PMID22326222
PMCPMC3314949
OpenAlexW2078057245

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.