Evidence map›Paper›PMID 38825692›Full record

ArticleGenome biology2024

Predicting gene expression state and prioritizing putative enhancers using 5hmC signal.

Edahi Gonzalez-Avalos, Atsushi Onodera, Daniela Samaniego-Castruita, Anjana Rao, Ferhat Ay

Abstract read
In one paragraph

Article in Genome biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Cell identity and 5-hydroxymethylcytosine.Epigenetics & chromatin · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. 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

5 authors.

Edahi Gonzalez-AvalosLa Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA.ORCID 0000-0002-6817-4854
Atsushi OnoderaLa Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA.ORCID 0000-0002-3715-9408
Daniela Samaniego-CastruitaLa Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA.ORCID 0000-0001-6082-6603
Anjana RaoLa Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA. arao@lji.org.ORCID 0000-0002-1870-1775
Ferhat AyLa Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA. ferhatay@lji.org.ORCID 0000-0002-0708-6914

Funding

SIGNAL TRANSDUCTION AND GENE INDUCTION IN T LYMPHOCYTESR01AI040127 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI HOGAN, PATRICK, RAO, ANJANA · 1996 to 2025
$13.3M
The TET-DNMT-ASXL1-OGT axis: relevance to clonal hematopoiesis, heterochromatin integrity and cancerR35CA210043 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Anjana Rao · 2016 to 2026
$10.6M
NFAT, bZIP proteins, and transcriptional programs in lymphocytesR01AI109842 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Patrick Hogan, Anjana Rao · 2014 to 2026
$8.6M
Stimulating Neo-Antigen Specific T Cell Responses in Head and Neck CancersU01DE028227 · NIDCR · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI GUTKIND, JORGE SILVIO, RAO, ANJANA · 2018 to 2022
$4.6M
Studying the function of human genetic variation in the light of 3D genome organizationR35GM128938 · NIGMS · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Ferhat Ay · 2018 to 2026
$4.6M
Exploring the potential of TET inhibition in cancer immunotherapyR01CA247500 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 2020 to 2024
$2.7M
National Institute of Allergy and Infectious Diseases R01-AI040127National Institute of Allergy and Infectious Diseases R01-AI109842NCI NIH HHS R01 CA247500NCI NIH HHS R01-CA247500NCI NIH HHS R35 CA210043NCI NIH HHS R35-CA210043NIAID NIH HHS R01 AI040127NIAID NIH HHS R01 AI109842NIDCR NIH HHS U01 DE028227NIGMS NIH HHS R35 GM128938NIGMS NIH HHS R35-GM128938NIH HHS U01-DE28277
6 · The paper itself

Abstract

backgroundLike its parent base 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC) is a direct epigenetic modification of cytosines in the context of CpG dinucleotides. 5hmC is the most abundant oxidized form of 5mC, generated through the action of TET dioxygenases at gene bodies of actively-transcribed genes and at active or lineage-specific enhancers. Although such enrichments are reported for 5hmC, to date, predictive models of gene expression state or putative regulatory regions for genes using 5hmC have not been developed.

resultsHere, by using only 5hmC enrichment in genic regions and their vicinity, we develop neural network models that predict gene expression state across 49 cell types. We show that our deep neural network models distinguish high vs low expression state utilizing only 5hmC levels and these predictive models generalize to unseen cell types. Further, in order to leverage 5hmC signal in distal enhancers for expression prediction, we employ an Activity-by-Contact model and also develop a graph convolutional neural network model with both utilizing Hi-C data and 5hmC enrichment to prioritize enhancer-promoter links. These approaches identify known and novel putative enhancers for key genes in multiple immune cell subsets.

conclusionsOur work highlights the importance of 5hmC in gene regulation through proximal and distal mechanisms and provides a framework to link it to genome function. With the recent advances in 6-letter DNA sequencing by short and long-read techniques, profiling of 5mC and 5hmC may be done routinely in the near future, hence, providing a broad range of applications for the methods developed here.

Indexed as

5-MethylcytosineEnhancer Elements, GeneticDNA MethylationEpigenesis, GeneticGene Expression RegulationHumansNeural Networks, Computer5-hydroxymethylcytosine5-Methylcytosine

Identifiers

PMID38825692
PMCPMC11145787

What Socratic holds

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Registered trials

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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 Socratic graph.