Evidence map›Paper›PMID 34498072›Full record

ArticleMolecular biology and evolution2021

Selection on Accessible Chromatin Regions in Capsella grandiflora.

Robert Horvath, Emily B Josephs, Edouard Pesquet, John R Stinchcombe, Stephen I Wright, Douglas Scofield, Tanja Slotte

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 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

7 authors at 4 institutions in 3 countries.

Robert HorvathDepartment of Ecology, Environment and Plant Sciences, Science for Life Laboratory, Stockholm University, Stockholm, Sweden.ORCID 0000-0002-3221-8835
Emily B JosephsDepartment of Plant Biology, Michigan State University, Lansing, MI, USA.
Edouard PesquetDepartment of Ecology, Environment and Plant Sciences, Stockholm University, Stockholm, Sweden.
John R StinchcombeDepartment of Ecology and Evolutionary Biology, University of Toronto, Toronto, ON, Canada.
Stephen I WrightDepartment of Ecology and Evolutionary Biology, University of Toronto, Toronto, ON, Canada.ORCID 0000-0001-9973-9697
Douglas ScofieldDepartment of Ecology and Genetics, Uppsala University, Uppsala, Sweden.
Tanja SlotteDepartment of Ecology, Environment and Plant Sciences, Science for Life Laboratory, Stockholm University, Stockholm, Sweden.ORCID 0000-0001-6020-5102
Stockholm University · SEUniversity of Toronto · CAMichigan State University · USUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate estimates of genome-wide rates and fitness effects of new mutations are essential for an improved understanding of molecular evolutionary processes. Although eukaryotic genomes generally contain a large noncoding fraction, functional noncoding regions and fitness effects of mutations in such regions are still incompletely characterized. A promising approach to characterize functional noncoding regions relies on identifying accessible chromatin regions (ACRs) tightly associated with regulatory DNA. Here, we applied this approach to identify and estimate selection on ACRs in Capsella grandiflora, a crucifer species ideal for population genomic quantification of selection due to its favorable population demography. We describe a population-wide ACR distribution based on ATAC-seq data for leaf samples of 16 individuals from a natural population. We use population genomic methods to estimate fitness effects and proportions of positively selected fixations (α) in ACRs and find that intergenic ACRs harbor a considerable fraction of weakly deleterious new mutations, as well as a significantly higher proportion of strongly deleterious mutations than comparable inaccessible intergenic regions. ACRs are enriched for expression quantitative trait loci (eQTL) and depleted of transposable element insertions, as expected if intergenic ACRs are under selection because they harbor regulatory regions. By integrating empirical identification of intergenic ACRs with analyses of eQTL and population genomic analyses of selection, we demonstrate that intergenic regulatory regions are an important source of nearly neutral mutations. These results improve our understanding of selection on noncoding regions and the role of nearly neutral mutations for evolutionary processes in outcrossing Brassicaceae species.

Indexed as

CapsellaChromatinDNA Transposable ElementsGenome, PlantHumansSelection, GeneticChromatinDNA Transposable ElementsATAC-sequencingdistribution of fitness effectsfunctional noncoding sequencesgene expression variationnatural selectionopen chromatin region

Identifiers

PMID34498072
PMCPMC8662636
OpenAlexW3014986240

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.