Evidence map›Paper›PMID 38225662›Full record

ArticleGenome biology2024

Chromatin activity identifies differential gene regulation across human ancestries.

Kade P Pettie, Maxwell Mumbach, Amanda J Lea, Julien Ayroles, Howard Y Chang, Maya Kasowski, Hunter B Fraser

Open access · goldAbstract 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

7 authors at 5 institutions in 1 country.

Kade P PettieDepartment of Biology, Stanford University, Stanford, CA, USA.
Maxwell MumbachDepartment of Genetics, Stanford University, Stanford, CA, USA.
Amanda J LeaDepartment of Biological Sciences, Vanderbilt University, Nashville, TN, USA.
Julien AyrolesDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.
Howard Y ChangCenter for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA, USA.
Maya KasowskiSean N. Parker Center for Allergy and Asthma Research, Stanford University School of Medicine, Stanford, CA, USA.
Hunter B FraserDepartment of Biology, Stanford University, Stanford, CA, USA. hbfraser@stanford.edu.ORCID 0000-0001-8400-8541
Stanford University · USHoward Hughes Medical Institute · USPrinceton University · USStanford Medicine · USVanderbilt University · US

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Center for Personal Dynamic RegulomesRM1HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2019 to 2023
$13.8M
A path to personalized phenotypic prediction: unlocking the context-dependency of allelic effectsR35GM124881 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Julien Ayroles · 2017 to 2026
$3.7M
Improved methods for inference of genotype-specific response to environmental toxinsR01ES029929 · NIEHS · PRINCETON UNIVERSITY · PI AYROLES, JULIEN, CLARK, ANDREW G · 2019 to 2023
$3.6M
Investigating human cis-regulatory evolution with hybrid iPS cellsR01HG012285 · NHGRI · STANFORD UNIVERSITY · PI FRASER, HUNTER B · 2022 to 2025
$2.8M
High-throughput precision genome editing to characterize natural genetic variantsR01GM134228 · NIGMS · STANFORD UNIVERSITY · PI FRASER, HUNTER B · 2019 to 2022
$1.8M
NHGRI NIH HHS R01 HG012285NHGRI NIH HHS RM1 HG007735NIEHS NIH HHS R01 ES029929NIGMS NIH HHS R01 GM134228NIGMS NIH HHS R35 GM124881NIGMS NIH HHS T32 GM007276NIH HHS R01-HG012285NIH HHS RM1-HG007735NIH HHS T32GM007276
6 · The paper itself

Abstract

backgroundCurrent evidence suggests that cis-regulatory elements controlling gene expression may be the predominant target of natural selection in humans and other species. Detecting selection acting on these elements is critical to understanding evolution but remains challenging because we do not know which mutations will affect gene regulation.

resultsTo address this, we devise an approach to search for lineage-specific selection on three critical steps in transcriptional regulation: chromatin activity, transcription factor binding, and chromosomal looping. Applying this approach to lymphoblastoid cells from 831 individuals of either European or African descent, we find strong signals of differential chromatin activity linked to gene expression differences between ancestries in numerous contexts, but no evidence of functional differences in chromosomal looping. Moreover, we show that enhancers rather than promoters display the strongest signs of selection associated with sites of differential transcription factor binding.

conclusionsOverall, our study indicates that some cis-regulatory adaptation may be more easily detected at the level of chromatin than DNA sequence. This work provides a vast resource of genomic interaction data from diverse human populations and establishes a novel selection test that will benefit future study of regulatory evolution in humans and other species.

Indexed as

ChromatinEnhancer Elements, GeneticGene Expression RegulationHumansPromoter Regions, GeneticTranscription FactorsChromatinTranscription FactorsActivity-by-ContactbQTLCis-regulationDirectional selectionEnhancerGene expressionHiChIPHumanLCL

Identifiers

PMID38225662
PMCPMC10789071
OpenAlexW4390885495

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.