Evidence map›Paper›PMID 35022759›Full record

ArticleMolecular biology and evolution2022

Demographic History and Natural Selection Shape Patterns of Deleterious Mutation Load and Barriers to Introgression across Populus Genome.

Shuyu Liu, Lei Zhang, Yupeng Sang, Qiang Lai, Xinxin Zhang, Changfu Jia, Zhiqin Long, Jiali Wu, Tao Ma, Kangshan Mao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
10.8field-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

39 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Repeated genetic adaptation under demographic limits in kiwifruit.The Plant journal : for cell and molecular biology · 2026
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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

14 authors at 3 institutions in 2 countries.

Shuyu LiuKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Lei ZhangKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Yupeng SangKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Qiang LaiKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Xinxin ZhangKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Changfu JiaKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Zhiqin LongKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Jiali WuKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Tao MaKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.ORCID 0000-0002-7094-6868
Kangshan MaoKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Nathaniel R StreetDepartment of Plant Physiology, Umeå Plant Science Centre, Umeå University, Umeå, Sweden.ORCID 0000-0001-6031-005X
Pär K IngvarssonDepartment of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden.ORCID 0000-0001-9225-7521
Jianquan LiuKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.
Jing WangKey Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science & State Key Lab of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China.ORCID 0000-0002-3793-3264
Sichuan University · CNSwedish University of Agricultural Sciences · SEUmeå Plant Science Centre · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hybridization and resulting introgression are important processes shaping the tree of life and appear to be far more common than previously thought. However, how the genome evolution was shaped by various genetic and evolutionary forces after hybridization remains unresolved. Here we used whole-genome resequencing data of 227 individuals from multiple widespread Populus species to characterize their contemporary patterns of hybridization and to quantify genomic signatures of past introgression. We observe a high frequency of contemporary hybridization and confirm that multiple previously ambiguous species are in fact F1 hybrids. Seven species were identified, which experienced different demographic histories that resulted in strikingly varied efficacy of selection and burdens of deleterious mutations. Frequent past introgression has been found to be a pervasive feature throughout the speciation of these Populus species. The retained introgressed regions, more generally, tend to contain reduced genetic load and to be located in regions of high recombination. We also find that in pairs of species with substantial differences in effective population size, introgressed regions are inferred to have undergone selective sweeps at greater than expected frequencies in the species with lower effective population size, suggesting that introgression likely have higher potential to provide beneficial variation for species with small populations. Our results, therefore, illustrate that demography and recombination have interplayed with both positive and negative selection in determining the genomic evolution after hybridization.

Indexed as

Genome, PlantPopulusHybridization, GeneticMutationSelection, Geneticadaptive introgressiongenetic loadhybridizationnatural selectionPopulus

Identifiers

PMID35022759
PMCPMC8826634
OpenAlexW4205202594

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.