Evidence map›Paper›PMID 40106667›Full record

ArticleGenetics2025

New perspectives on Drosophila melanogaster de novo gene origination revealed by investigation of ancient African genetic variation.

Julie M Cridland, Elizabeth S Polston, David J Begun

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. De Novo Genes: Current Status and Future Goals.Genome biology and evolution · 2025
    Article
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

3 authors.

Julie M CridlandDepartment of Evolution and Ecology, University of California, Davis, Davis, CA 95616, USA.
Elizabeth S PolstonDepartment of Evolution and Ecology, University of California, Davis, Davis, CA 95616, USA.ORCID 0009-0009-3763-537X
David J BegunDepartment of Evolution and Ecology, University of California, Davis, Davis, CA 95616, USA.

Funding

Evolutionary and functional genomics of genetic novelties and expression adaptation in DrosophilaR35GM134930 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BEGUN, DAVID J · 2020 to 2024
$2.2M
Evolutionary and functional genomics of genetic novelties and expression adaptation in DrosophilaR35GM156525 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DAVID J BEGUN · 2025 to 2026
$1.0M
NIGMS NIH HHS R35 GM134930NIGMS NIH HHS R35 GM156525NIH HHS NIGMS R35GM134930
6 · The paper itself

Abstract

De novo genes can be defined as sequences producing evolutionarily derived transcripts that are not homologous to transcripts produced in an ancestor. While they appear to be taxonomically widespread, there is little agreement regarding their abundance, their persistence times in genomes, the population genetic processes responsible for their spread or loss, or their possible functions. In Drosophila melanogaster, 2 approaches have been used to discover these genes and investigate their properties. One uses traditional comparative approaches and existing genomic resources and annotations. A second approach uses raw transcriptome data to discover unannotated genes for which there is no evidence of presence in related species. Investigations using the second approach have focused on D. melanogaster genotypes from recently established cosmopolitan populations. However, most of the genetic variation in the species is found in African populations, suggesting the possibility that fuller understanding of genetic novelties in the species may follow from studies of these populations. Here, we investigate de novo gene candidates expressed in testis and accessory glands in a sample of flies from Zambia and compare them with candidate de novo genes expressed in North American populations. We report a large number of previously undiscovered de novo gene candidates, most of which are expressed polymorphically. Many are predicted to code for secreted proteins. In spite of much different levels of genomic variation in Zambian and North American populations, they express similar numbers of candidate de novo genes. We find evidence from genetic analysis of Raleigh inbred lines that a fraction of rarely expressed gene candidates in this population represent deleterious transcription promoted by inbreeding depression. Many de novo gene candidates are expressed in multiple tissues and both sexes, raising questions about how they may interact with natural selection. The relative importance of positive and negative selection, however, remains unclear.

Indexed as

Drosophila melanogasterEvolution, MolecularGenetic VariationAfricaAnimalsFemaleMaleTranscriptomede novo genesDrosophilagene expressionpopulation genomicsZambia

Identifiers

PMID40106667
PMCPMC12059636

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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.