Evidence map›Paper›PMID 30420518›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Histone H3 lysine 4 methylation signature associated with human undernutrition.

Robin Uchiyama, Kristyna Kupkova, Savera J Shetty, Alicia S Linford, Marilyn G Pray-Grant, Lisa E Wagar, Mark M Davis, Rashidul Haque, Alban Gaultier, Marty W Mayo and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

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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

14 authors at 4 institutions in 3 countries.

Robin UchiyamaDivision of Infectious Diseases and International Health, University of Virginia Health System, Charlottesville, VA 22908.
Kristyna KupkovaDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908.ORCID 0000-0002-6774-2709
Savera J ShettyDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908.
Alicia S LinfordDivision of Infectious Diseases and International Health, University of Virginia Health System, Charlottesville, VA 22908.
Marilyn G Pray-GrantDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908.
Lisa E WagarDepartment of Microbiology and Immunology, Stanford University, Stanford, CA 94305.
Mark M DavisDepartment of Microbiology and Immunology, Stanford University, Stanford, CA 94305.
Rashidul HaqueLaboratory Sciences Division, International Centre for Diarrhoeal Disease Research, Dhaka 1000, Bangladesh.
Alban GaultierDepartment of Neuroscience, Center for Brain Immunology and Glia, University of Virginia Health System, Charlottesville, VA 22908.
Marty W MayoDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908.
Patrick A GrantDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908.
William A PetriDivision of Infectious Diseases and International Health, University of Virginia Health System, Charlottesville, VA 22908.
Stefan BekiranovDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908.
David T AubleDepartment of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, VA 22908; auble@virginia.edu.
University of Virginia Health System · USHoward Hughes Medical Institute · USInternational Centre for Diarrhoeal Disease Research · BDStanford University · US

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
FIELD STUDIES OF IMMUNITY TO AMEBIASIS IN BANGLADESHR01AI043596 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CAROL A GILCHRIST, William A Petri · 1998 to 2026
$7.7M
Identifying tumor suppressor targets of SIRT6 in lung cancerR01CA192399 · NCI · UNIVERSITY OF VIRGINIA · PI MAYO, MARTY W · 2015 to 2019
$1.9M
Role of LRP1 in NF-kB mediated neuroinflammationR01NS083542 · NINDS · UNIVERSITY OF VIRGINIA · PI GAULTIER, ALBAN P · 2015 to 2019
$1.9M
NCI NIH HHS R01 CA192399NIAID NIH HHS R01 AI043596NIAID NIH HHS U19 AI057229NINDS NIH HHS R01 NS083542
6 · The paper itself

Abstract

Chronically undernourished children become stunted during their first 2 years and thereafter bear burdens of ill health for the rest of their lives. Contributors to stunting include poor nutrition and exposure to pathogens, and parental history may also play a role. However, the epigenetic impact of a poor environment on young children is largely unknown. Here we show the unfolding pattern of histone H3 lysine 4 trimethylation (H3K4me3) in children and mothers living in an urban slum in Dhaka, Bangladesh. A pattern of chromatin modification in blood cells of stunted children emerges over time and involves a global decrease in methylation at canonical locations near gene start sites and increased methylation at ectopic sites throughout the genome. This redistribution occurs at metabolic and immune genes and was specific for H3K4me3, as it was not observed for histone H3 lysine 27 acetylation in the same samples. Methylation changes in stunting globally resemble changes that occur in vitro in response to altered methylation capacity, suggesting that reduced levels of one-carbon nutrients in the diet play a key role in stunting in this population. A network of differentially expressed genes in stunted children reveals effects on chromatin modification machinery, including turnover of H3K4me3, as well as posttranscriptional gene regulation affecting immune response pathways and lipid metabolism. Consistent with these changes, reduced expression of the endocytic receptor gene LDL receptor 1 (LRP1) is a driver of stunting in a mouse model, suggesting a target for intervention.

Indexed as

AnimalsEpigenesis, GeneticFemaleHistonesHumansInfantInfant, NewbornMaleMalnutritionMethylationMicehistone H3 trimethyl Lys4Histonesepigeneticshistone methylationundernutrition

Identifiers

PMID30420518
PMCPMC6275549
OpenAlexW2900705702

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.