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Sexual life cycle establishes the unicellular red algae Cyanidiophyceae as a genetically tractable model lineage for eukaryotic evolution
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Sexual life cycle establishes the unicellular red algae Cyanidiophyceae as a genetically tractable model lineage for…

Shunsuke Hirooka, Takayuki Fujiwara, Mark Seger +15 more
October 2025
 ·
bioRxiv
 ·
DOI 
10.1101/2025.10.15.681507
94
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Why this is interesting

Discovering sexual life cycles across Cyanidiophyceae and reclassifying C. merolae 10D as haploid resolves fundamental mysteries in early plant evolution and transforms this ancient lineage into a genetically tractable model for dissecting conserved eukaryotic mechanisms.

Author perspective

What is the most important insight, discovery, or finding from your paper that you would like other scientists to know?
“

We elucidated sexual life cycles in all cultivable genera of the unicellular red algal class Cyanidiophyceae, an early-diverging lineage within Archaeplastida comprising red algae, glaucophytes, green algae, and land plants. Together with genomic resources and genetic manipulation systems, these advances establish Cyanidiophyceae as a powerful model lineage for studying the evolution of sex, life cycles, epigenetic regulation, and environmental adaptation in Archaeplastida, with broader implications for eukaryotic evolution.

”
Shunsuke Hirooka

QED claims analysis

Summary

The unicellular red algal class Cyanidiophyceae undergoes sexual reproduction through isogamous mating between cell wall-less haploid cells that form cell-walled diploids, with life cycle transitions regulated by H3K27me3-mediated epigenetic control of phase-specific gene expression including conserved transcription factor families, and organelle DNA inheritance proceeding through initial biparental inheritance that resolves to uniparental inheritance during diploid proliferation, establishing Cyanidiophyceae as a genetically tractable model lineage with streamlined genomes for studying early Archaeplastida evolution and eukaryotic life cycle mechanisms.

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Main Claim 1 –

Cyanidiophyceae exhibit haploid–diploid sexual life cycles

Supporting evidence

  • Meiotic recombination generates distinct SNP/indel haploid progeny patterns
  • Diploids dominate natural habitats; haploids mainly laboratory-derived
  • PEG transformation enables genetics in haploids across Cyanidiophyceae
  • Streamlined Cyanidiophyceae genomes retain sexual reproduction machinery
  • Phase-dependent stress tolerance with species-specific metal resistance
Main Claim 2 –

Isogamous mating with biparental organelles resolving to uniparental inheritance

Main Claim 3 –

H3K27me3 regulates phase-specific expression of conserved transcription factors

Supporting evidence

  • Diploid-biased cell wall gene expression matches phase morphology
  • Phase-specific cytokinesis: diploid actin-ring versus haploid ESCRT-III

Abstract

The thermo-acidophilic unicellular algal class Cyanidiophyceae is the earliest-branching lineage in red algae, which diverged from Viridiplantae lineage (green algae and land plants) soon after chloroplast establishment in the common ancestor of Archaeplastida. Cyanidiophyceae possess extremely simple genomes (8.7–17.8 Mb; approximately 4,800– 7,800 genes), and the cell-wall-less, genetically tractable strain Cyanidioschyzon merolae 10D has served as a model organism. However, its unknown sexual life cycle has limited its utility in studies of evolution and genetics. Inspired by the recent discovery of sexual reproduction in the cyanidiophycean genus Galdieria, we identified similar life cycles in the other cyanidiophycean genera Cyanidioschyzon, Cyanidiococcus, and Cyanidium. In these genera, the cell-walled diploid form, exclusively observed in nature, produces a cell-wall-less haploid form when the culture pH is lowered, and both proliferate asexually. In addition, the cell-wall-less Cyanidioschyzon merolae 10D strain has been shown to be a haploid clone that forms a cell-walled diploid through mating with other haploid clones. Building on these findings, we generated high-quality genomic resources with phase-specific transcriptomes and developed genetic manipulation systems using the cell-wall-less haploids of these genera. We further uncovered phase-specific distribution of histone H3 lysine 27 trimethylation linked to haploid- and diploid-specific gene expression, including transcription factors involved in differentiation associated with sexual reproduction in plants. Additionally, biparental inheritance of organelle DNA occurs following isogamous mating of haploid cells but resolves into uniparental inheritance during diploid proliferation. These advances position Cyanidiophyceae as a powerful model lineage for studying early Archaeplastida evolution, the shared mechanisms of photosynthetic eukaryotes, and their environmental adaptation.

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