Evidence map›Paper›PMID 32719115›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

DNA methylation enables transposable element-driven genome expansion.

Wanding Zhou, Gangning Liang, Peter L Molloy, Peter A Jones

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
24.3field-weighted citation impact, top 1% 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

104 citing papers in PubMed, 194 citations in OpenAlex.

  1. Machine learning reveals sequence and genomic context features underlyingbioRxiv : the preprint server for biology · 2026
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  3. The genome of a keystone predator: adaptive innovations in Charonia tritonis drive specialized predation and coral reef resilience.DNA research : an international journal for rapid publication of reports on genes and genomes · 2026
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44 more citing papers are in PubMed but not listed here.

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

4 authors at 4 institutions in 2 countries.

Wanding ZhouCenter for Computational and Genomic Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA 19104; zhouw3@email.chop.edu peter.jones@vai.org.ORCID 0000-0001-9126-1932
Gangning LiangDepartment of Urology, USC Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA 90089.
Peter L MolloyNutrition and Health Program, Health and Biosecurity, Commonwealth Scientific and Industrial Research Organisation, North Ryde, NSW 2113, Australia.ORCID 0000-0002-7788-3417
Peter A JonesCenter for Epigenetics, Van Andel Institute, Grand Rapids, MI 49503 zhouw3@email.chop.edu peter.jones@vai.org.ORCID 0000-0001-8309-4767
Children's Hospital of Philadelphia · USCommonwealth Scientific and Industrial Research Organisation · AUUniversity of Southern California · USVan Andel Institute · US

Funding

Targeting DNA Methylation and the Cancer EpigenomeR35CA209859 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI PETER A JONES · 2017 to 2026
$11.9M
NCI NIH HHS R35 CA209859
6 · The paper itself

Abstract

Multicellular eukaryotic genomes show enormous differences in size. A substantial part of this variation is due to the presence of transposable elements (TEs). They contribute significantly to a cell's mass of DNA and have the potential to become involved in host gene control. We argue that the suppression of their activities by methylation of the C-phosphate-G (CpG) dinucleotide in DNA is essential for their long-term accommodation in the host genome and, therefore, to its expansion. An inevitable consequence of cytosine methylation is an increase in C-to-T transition mutations via deamination, which causes CpG loss. Cytosine deamination is often needed for TEs to take on regulatory functions in the host genome. Our study of the whole-genome sequences of 53 organisms showed a positive correlation between the size of a genome and the percentage of TEs it contains, as well as a negative correlation between size and the CpG observed/expected (O/E) ratio in both TEs and the host DNA. TEs are seldom found at promoters and transcription start sites, but they are found more at enhancers, particularly after they have accumulated C-to-T and other mutations. Therefore, the methylation of TE DNA allows for genome expansion and also leads to new opportunities for gene control by TE-based regulatory sites.

Indexed as

DNA MethylationGenomeCpG IslandsCytosineDNA Transposable ElementsEukaryotaGene Expression RegulationGenome SizeMutationPromoter Regions, GeneticCytosineDNA Transposable ElementsDNA methylationgenome sizetransposable element

Identifiers

PMID32719115
PMCPMC7431005
OpenAlexW3046171324

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.