Evidence map›Paper›PMID 39152327›Full record

ArticleNature ecology & evolution2024

Parallel loss of sexual reproduction in field populations of a brown alga sheds light on the mechanisms underlying the emergence of asexuality.

Masakazu Hoshino, Guillaume Cossard, Fabian B Haas, Emma I Kane, Kazuhiro Kogame, Takahiro Jomori, Toshiyuki Wakimoto, Sylvain Glemin, Susana M Coelho

Abstract read
In one paragraph

Article in Nature ecology & evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Germline fate determination by a single ARGONAUTE protein inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. 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

9 authors.

Masakazu HoshinoDepartment of Algal Development and Evolution, Max Planck Institute for Biology Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0003-3631-5429
Guillaume CossardDepartment of Algal Development and Evolution, Max Planck Institute for Biology Tübingen, Tübingen, Germany.
Fabian B HaasDepartment of Algal Development and Evolution, Max Planck Institute for Biology Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-7711-5282
Emma I KaneDepartment of Algal Development and Evolution, Max Planck Institute for Biology Tübingen, Tübingen, Germany.
Kazuhiro KogameDepartment of Biological Sciences, Faculty of Science, Hokkaido University, Sapporo, Japan.
Takahiro JomoriFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Toshiyuki WakimotoFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.ORCID http://orcid.org/0000-0003-2917-1797
Sylvain GleminLaboratoire ECOBIO (Ecosystèmes, biodiversité, évolution), UMR 6553, CNRS, Université de Rennes, Rennes, France.
Susana M CoelhoDepartment of Algal Development and Evolution, Max Planck Institute for Biology Tübingen, Tübingen, Germany. susana.coelho@tuebingen.mpg.de.ORCID http://orcid.org/0000-0002-9171-2550

Funding

EC | EC Seventh Framework Programm | FP7 Ideas: European Research Council (FP7-IDEAS-ERC - Specific Programme: "Ideas" Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013)) 864038Gordon and Betty Moore Foundation (Gordon E. and Betty I. Moore Foundation) GBMF11489
6 · The paper itself

Abstract

Sexual reproduction is widespread, but asexual lineages have repeatedly arisen from sexual ancestors across a wide range of eukaryotic taxa. The molecular changes underpinning the switch to asexuality remain elusive, particularly in organisms with haploid sexual systems. Here we explore independent events of loss of sex in the brown alga Scytosiphon, examine the proximate and evolutionary mechanisms involved, and test the importance of sexual conflict on gene expression changes following loss of sex. We find that asexual females ('Amazons') lose ability to produce sex pheromone and, consequently, are incapable of attracting males, whereas they gain rapid parthenogenic development from large, unfertilized eggs. These phenotypic changes are accompanied by convergent changes in gene expression. Decay of female functions, rather than relaxation of sexual antagonism, may be a dominant force at play during the emergence of asexuality in haploid sexual systems. Moreover, we show that haploid purifying selection plays a key role in limiting the accumulation of deleterious alleles in Amazons, and we identify an autosomal locus associated with the Amazon phenotype. The sex chromosome, together with this autosomal locus, may underlie the switch to obligate asexuality in the Amazon populations.

Indexed as

PhaeophyceaeReproduction, AsexualBiological EvolutionHaploidyReproduction

Identifiers

PMID39152327
PMCPMC11461277

What OpenQuestion holds

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LicenceCC BY
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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.