Evidence map›Paper›PMID 40587577›Full record

ArticlePLoS biology2025

The evolution of separate sexes in waterhemp is associated with surprising chromosomal diversity and complexity.

Julia M Kreiner, Jacob S Montgomery, Marco Todesco, Natalia Bercovich, Yunchen Gong, Cassandra Elphinstone, Patrick J Tranel, Loren H Rieseberg, Stephen I Wright

Abstract read
In one paragraph

Article in PLoS biology, 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. 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.

Julia M KreinerDepartment of Ecology & Evolution, University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-8593-1394
Jacob S MontgomeryDepartment of Ecology & Evolution, University of Chicago, Chicago, Illinois, United States of America.
Marco TodescoMichael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
Natalia BercovichBiodiversity Research Centre and Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada.
Yunchen GongCenter for the Analysis of Genome Evolution and Function, University of Toronto, Toronto, Ontario, Canada.
Cassandra ElphinstoneBiodiversity Research Centre and Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada.
Patrick J TranelDepartment of Crop Sciences, University of Illinois Urbana-Champaign, Champaign, Illinois, United States of America.
Loren H RiesebergBiodiversity Research Centre and Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada.
Stephen I WrightCenter for the Analysis of Genome Evolution and Function, University of Toronto, Toronto, Ontario, Canada.

Funding

Canada Research Chair in Population GenomicsUBC Bioinformatic Biodiversity Research Centre FellowshipUniversity of ChicagoUSDA NIFA 2022-67013-36142Weston Award in Northern Research
6 · The paper itself

Abstract

The evolution of separate sexes is hypothesized to occur through distinct pathways involving few large-effect or many small-effect alleles. However, we lack empirical evidence for how these different genetic architectures shape the transition from quantitative variation in sex expression to distinct male and female phenotypes. To explore these processes, we leveraged the recent transition of Amaranthus tuberculatus to dioecy within a predominantly monoecious genus, along with a sex-phenotyped population genomic dataset, and six newly generated chromosome-level haplotype phased assemblies. We identify a ~3 Mb region strongly associated with sex through complementary SNP genotype and sequence-depth-based analyses. Comparative genomics of these proto-sex chromosomes within the species and across the Amaranthus genus demonstrates remarkable variability in their structure and genic content, including numerous polymorphic inversions. No such inversion underlies the extended linkage we observe associated with sex determination. Instead, we identify a complex presence/absence polymorphism reflecting substantial Y-haplotype variation-structured by ancestry, geography, and habitat-but only partially explaining phenotyped sex. Just over 10% of sexed individuals show phenotype-genotype mismatch in the sex-linked region, and along with observation of leakiness in the phenotypic expression of sex, suggest additional modifiers of sex and dynamic gene content within and between the proto-X and Y. Together, this work reveals a complex genetic architecture of sex determination in A. tuberculatus characterized by the maintenance of substantial haplotype diversity, and variation in the expression of sex.

Indexed as

Biological EvolutionChromosomes, PlantEvolution, MolecularGenetic VariationHaplotypesPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID40587577
PMCPMC12237273

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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.