Evidence map›Paper›PMID 32619550›Full record

ArticleCell systems2020

Quantitative Translation of Dog-to-Human Aging by Conserved Remodeling of the DNA Methylome.

Tina Wang, Jianzhu Ma, Andrew N Hogan, Samson Fong, Katherine Licon, Brian Tsui, Jason F Kreisberg, Peter D Adams, Anne-Ruxandra Carvunis, Danika L Bannasch and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cell systems, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 2% 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

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 132 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Developmental programming in dogs.Biology of reproduction · 2026
    Review
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  13. Review
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  19. Workshop Report-Heterogeneity and Successful Aging Part I: Heterogeneity in Aging-Challenges and Opportunities.The journals of gerontology. Series A, Biological sciences and medical sciences · 2025
    Article
  20. Article

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Tina WangDivision of Genetics, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Jianzhu MaDivision of Genetics, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Andrew N HoganNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Samson FongDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Katherine LiconDivision of Genetics, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Brian TsuiDivision of Genetics, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Jason F KreisbergDivision of Genetics, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Peter D AdamsSanford Burnham Prebys Medical Discovery Institute, San Diego, La Jolla, CA 92093, USA.
Anne-Ruxandra CarvunisDepartment of Computational and Systems Biology, Pittsburgh Center for Evolutionary Biology and Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Danika L BannaschDepartment of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, Davis, CA, USA.
Elaine A OstranderNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Trey IdekerDivision of Genetics, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA; Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA. Electronic address: tideker@ucsd.edu.
University of California, San Diego · USDiscovery Institute · USNational Human Genome Research Institute · USNational Institutes of Health · USUniversity of California, Davis · USUniversity of Pittsburgh · US

Funding

STRUCTURAL BASIS FOR EPIGENETICS IN AGING AND LONGEVITYP01AG031862 · NIA · WISTAR INSTITUTE · PI BERGER, SHELLEY L · 2008 to 2022
$28.3M
Comparative Mammalian GenomicsZIAHG200377 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI OSTRANDER, ELAINE · 2012 to 2025
$24.8M
Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
A Systems Approach to Mapping the DNA Damage ResponseR01ES014811 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI IDEKER, TREY · 2005 to 2021
$8.6M
UC San Diego Genetics Training ProgramT32GM145427 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BRUCE A HAMILTON · 2022 to 2026
$2.6M
Molecular characterization of novel loci for orofacial clefting using canine modeR01DE022532 · NIDCR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BANNASCH, DANIKA L · 2011 to 2014
$2.1M
Deciphering the mechanisms and dynamics of proto-gene evolutionR00GM108865 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CARVUNIS, ANNE-RUXANDRA · 2017 to 2019
$747k
Deciphering the mechanisms and dynamics of proto-gene evolutionK99GM108865 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CARVUNIS, ANNE-RUXANDRA · 2014 to 2015
$180k
NIA NIH HHS P01 AG031862NIDCR NIH HHS R01 DE022532NIEHS NIH HHS R01 ES014811NIGMS NIH HHS K99 GM108865NIGMS NIH HHS R00 GM108865NIGMS NIH HHS T32 GM008666NIGMS NIH HHS T32 GM145427
6 · The paper itself

Abstract

All mammals progress through similar physiological stages throughout life, from early development to puberty, aging, and death. Yet, the extent to which this conserved physiology reflects underlying genomic events is unclear. Here, we map the common methylation changes experienced by mammalian genomes as they age, focusing on comparison of humans with dogs, an emerging model of aging. Using oligo-capture sequencing, we characterize methylomes of 104 Labrador retrievers spanning a 16-year age range, achieving >150× coverage within mammalian syntenic blocks. Comparison with human methylomes reveals a nonlinear relationship that translates dog-to-human years and aligns the timing of major physiological milestones between the two species, with extension to mice. Conserved changes center on developmental gene networks, which are sufficient to translate age and the effects of anti-aging interventions across multiple mammals. These results establish methylation not only as a diagnostic age readout but also as a cross-species translator of physiological aging milestones.

Indexed as

AgingAnimalsDNA MethylationDogsHumansagingcaninedogepigenetic agingepigenetic clockepigeneticsepigenomeevolutionmethylationmethylome

Identifiers

PMID32619550
PMCPMC7484147
OpenAlexW3039634063

What OpenQuestion holds

Textmetadata
LicenceTDM
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.