Evidence map›Paper›PMID 39020011›Full record

ArticleScientific reports2024

The rate of W chromosome degeneration across multiple avian neo-sex chromosomes.

Hanna Sigeman, Philip A Downing, Hongkai Zhang, Bengt Hansson

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Genomic origins and evolution of neo-sex chromosomes in Pacific Island birds.Proceedings of the National Academy of Sciences of the United States of America · 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

4 authors.

Hanna SigemanDepartment of Biology, Lund University, Ecology Building, 223 62, Lund, Sweden. hanna.sigeman@oulu.fi.ORCID 0000-0002-1457-4174
Philip A DowningEcology and Genetics Research Unit, University of Oulu, Oulu, Finland.ORCID 0000-0002-5286-3153
Hongkai ZhangDepartment of Biology, Lund University, Ecology Building, 223 62, Lund, Sweden.ORCID 0000-0001-7371-9612
Bengt HanssonDepartment of Biology, Lund University, Ecology Building, 223 62, Lund, Sweden. bengt.hansson@biol.lu.se.ORCID 0000-0001-6694-8169

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When sex chromosomes evolve recombination suppression, the sex-limited chromosome (Y/W) commonly degenerate by losing functional genes. The rate of Y/W degeneration is believed to slow down over time as the most essential genes are maintained by purifying selection, but supporting data are scarce especially for ZW systems. Here, we study W degeneration in Sylvioidea songbirds where multiple autosomal translocations to the sex chromosomes, and multiple recombination suppression events causing separate evolutionary strata, have occurred during the last ~ 28.1-4.5 million years (Myr). We show that the translocated regions have maintained 68.3-97.7% of their original gene content, compared to only 4.2% on the much older ancestral W chromosome. By mapping W gene losses onto a dated phylogeny, we estimate an average gene loss rate of 1.0% per Myr, with only moderate variation between four independent lineages. Consistent with previous studies, evolutionarily constrained and haploinsufficient genes were preferentially maintained on W. However, the gene loss rate did not show any consistent association with strata age or with the number of W genes at strata formation. Our study provides a unique account on the pace of W gene loss and reinforces the significance of purifying selection in maintaining essential genes on sex chromosomes.

Indexed as

Evolution, MolecularSex ChromosomesAnimalsFemaleMalePhylogenySongbirdsTranslocation, GeneticNeo-sex chromosomeRate of gene lossSex chromosomeSylvioideaW chromosome degeneration

Identifiers

PMID39020011
PMCPMC11255319

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