Evidence map›Paper›PMID 40791346›Full record

ArticlebioRxiv : the preprint server for biology2025

Programmed DNA elimination drives rapid genomic innovation in two thirds of all bird species.

Francisco J Ruiz-Ruano, Stephen A Schlebusch, Niki Vontzou, Hugo Moreno, Matthew T Biegler, Verena E Kutschera, Diana Ekman, Inês Borges, Yifan Pei, Roberto Rossini and 28 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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.

No citing paper in PubMed yet.

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

38 authors.

Francisco J Ruiz-RuanoCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig Bonn, Germany.ORCID 0000-0002-5391-301X
Stephen A SchlebuschDepartment of Zoology, Faculty of Science, Charles University, Czech Republic.
Niki VontzouCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig Bonn, Germany.
Hugo MorenoDepartment of Zoology, Faculty of Science, Charles University, Czech Republic.
Matthew T BieglerLaboratory of Neurogenetics of Language, The Rockefeller University, USA.
Verena E KutscheraDepartment of Biochemistry and Biophysics, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Stockholm University, Sweden.
Diana EkmanDepartment of Biochemistry and Biophysics, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Stockholm University, Sweden.
Inês BorgesCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig Bonn, Germany.
Yifan PeiCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig Bonn, Germany.
Roberto RossiniDepartment of Organismal Biology, Systematic Biology (EBC), Science for Life Laboratory, Uppsala University, Sweden.
Tomas AlbrechtDepartment of Zoology, Faculty of Science, Charles University, Czech Republic.
Jesper BomanDepartment of Ecology and Genetics, Uppsala University, Sweden.
Pavel BorodinInstitute of Cytology and Genetics, Russian Academy of Sciences, Russia.
Reto BurriSwiss Ornithological Institute, Switzerland.
Kristal E CainSchool of Biological Sciences, University of Auckland, New Zealand.
Wolfgang ForstmeierDepartment of Ornithology, Max Planck Institute for Biological Intelligence, Germany.
Carolina Frankl-VilchesDepartment of Behavioural Neurobiology, Max Planck Institute for Biological Intelligence, Germany.
Manfred GahrDepartment of Behavioural Neurobiology, Max Planck Institute for Biological Intelligence, Germany.
Simon C GriffithDepartment of Biological Sciences, Macquarie University, Australia.
Amy M HillBragato Research Institute, Lincoln, New Zealand.
Martin IrestedtDepartment of Bioinformatics and Genetics, Swedish Museum of Natural History, Sweden.
Leo JosephAustralian National Wildlife Collection, National Research Collections Australia, CSIRO, Australia.
Knud A JønssonDepartment of Bioinformatics and Genetics, Swedish Museum of Natural History, Sweden.
Takeshi KawakamiEmbark Veterinary, Inc., USA.
Bart KempenaersDepartment of Ornithology, Max Planck Institute for Biological Intelligence, Germany.
Lyubov MalinovskayaNovosibirsk State University, Russia.
Jakob C MuellerDepartment of Ornithology, Max Planck Institute for Biological Intelligence, Germany.
Edivaldo H C de OliveiraSeção de Meio Ambiente, Instituto Evandro Chagas, Ananindeua, PA, Brazil.
Octavio M Palacios-GimenezDepartment of Organismal Biology, Systematic Biology (EBC), Science for Life Laboratory, Uppsala University, Sweden.
Vaidas PalinauskasState Scientific Research Institute Nature Research Centre, Vilnius, Lithuania.
Anna QvarnströmDepartment of Ecology and Genetics, Uppsala University, Sweden.
Radka ReifovaDepartment of Zoology, Faculty of Science, Charles University, Czech Republic.
Jakub RidlDepartment of Zoology, Faculty of Science, Charles University, Czech Republic.
J Carolina SegamiDepartment of Ecology and Genetics, Uppsala University, Sweden.
David J X TanGerman Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Leipzig 04103, Germany.ORCID 0000-0001-7019-7871
Anna TorgashevaCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig Bonn, Germany.
Annabel WhibleySchool of Biological Sciences, University of Auckland, New Zealand.
Alexander SuhCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig Bonn, Germany.ORCID 0000-0002-8979-9992

Funding

Genomic Conflict Resolution: Establishment of a new model for unconstrained germline selectionK99HG014014 · NHGRI · ROCKEFELLER UNIVERSITY · PI Matthew Theodor Biegler · 2025 to 2026
$317k
NHGRI NIH HHS K99 HG014014
6 · The paper itself

Abstract

Bird genomes are among the most stable in terms of synteny and gene content across vertebrates. However, germline-restricted chromosomes (GRCs) represent a striking exception where programmed DNA elimination confines large-scale genomic changes to the germline. GRCs are known to occur in songbirds (oscines), but have been studied only in a few species of Passerides such as the zebra finch, the key model for passerine genomics. Their presence and evolutionary dynamics in most major passerine lineages remain largely unexplored, with suboscines entirely unexamined by cytogenetic or genomic methods. Here, we present the most comprehensive comparative analysis of GRCs to date, spanning 44 million years of passerine evolution. By generating the first germline reference genomes of an oscine and a suboscine, 22 novel germline draft genomes spanning nearly all major passerine lineages and a germline draft genome of a parrot outgroup, we show that the GRC is likely present in 6,700 passerine species. Our results reveal that the GRC evolves rapidly and distinctly from the standard A chromosomes (autosomes and sex chromosomes), yet retains functionally important, selectively maintained genes. We observed gene and repeat turnover occuring orders of magnitude faster than on the A chromosomes. Some GRC genes, such as

Identifiers

PMID40791346
PMCPMC12338730

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.