Evidence map›Paper›PMID 37214934›Full record

ArticlebioRxiv : the preprint server for biology2023

CpG island turnover events predict evolutionary changes in enhancer activity.

Acadia A Kocher, Emily V Dutrow, Severin Uebbing, Kristina M Yim, María F Rosales Larios, Marybeth Baumgartner, Timothy Nottoli, James P Noonan

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Acadia A KocherDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
Emily V DutrowDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
Severin UebbingDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
Kristina M YimDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
María F Rosales LariosDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
Marybeth BaumgartnerDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
Timothy NottoliDepartment of Comparative Medicine, Yale School of Medicine, New Haven, CT 06510, USA.
James P NoonanDepartment of Genetics, Yale School of Medicine, New Haven CT 06510, USA.
Yale University · USNational Institutes of Health · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007499 · NIGMS · YALE UNIVERSITY · PI CARLSON, JOHN R, REINKE, VALERIE J · 1985 to 2022
$13.9M
GENETICS AND GENOMICS OF HUMAN DISEASET32HD007149 · NICHD · YALE UNIVERSITY · PI James P Noonan · 1985 to 2026
$8.2M
Identifying enhancers with human-specific developmental functionsR01GM094780 · NIGMS · YALE UNIVERSITY · PI NOONAN, JAMES P · 2010 to 2018
$5.8M
Modeling uniquely human developmental gene regulatory networks using humanized miceR01HD102030 · NICHD · YALE UNIVERSITY · PI NOONAN, JAMES P · 2020 to 2024
$2.8M
Modeling gene regulatory mechanisms contributing to the evolution of the human cerebral cortexF32HD108935 · NICHD · YALE UNIVERSITY · PI BAUMGARTNER, MARY · 2022 to 2024
$225k
NICHD NIH HHS F32 HD108935NICHD NIH HHS R01 HD102030NICHD NIH HHS T32 HD007149NIGMS NIH HHS R01 GM094780NIGMS NIH HHS T32 GM007499
6 · The paper itself

Abstract

Genetic changes that modify the function of transcriptional enhancers have been linked to the evolution of biological diversity across species. Multiple studies have focused on the role of nucleotide substitutions, transposition, and insertions and deletions in altering enhancer function. Here we show that turnover of CpG islands (CGIs), which contribute to enhancer activation, is broadly associated with changes in enhancer activity across mammals, including humans. We integrated maps of CGIs and enhancer activity-associated histone modifications obtained from multiple tissues in nine mammalian species and found that CGI content in enhancers was strongly associated with increased histone modification levels. CGIs showed widespread turnover across species and species-specific CGIs were strongly enriched for enhancers exhibiting species-specific activity across all tissues and species we examined. Genes associated with enhancers with species-specific CGIs showed concordant biases in their expression, supporting that CGI turnover contributes to gene regulatory innovation. Our results also implicate CGI turnover in the evolution of Human Gain Enhancers (HGEs), which show increased activity in human embryonic development and may have contributed to the evolution of uniquely human traits. Using a humanized mouse model, we show that a highly conserved HGE with a large CGI absent from the mouse ortholog shows increased activity at the human CGI in the humanized mouse diencephalon. Collectively, our results point to CGI turnover as a mechanism driving gene regulatory changes potentially underlying trait evolution in mammals.

Identifiers

PMID37214934
PMCPMC10197647
OpenAlexW4376107947

What OpenQuestion 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 OpenQuestion graph.