ArticleGenome biology and evolution2025
Comparative Genomics of Chloropicon primus and Chloropicon roscoffensis Provide Insights into the Evolutionary Dynamics and Ecological Success of These Tiny Green Algae in Marine Environments.
Article in Genome biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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1 citing paper in PubMed.
- Genomic and transcriptomic basis of morphological and life cycle diversity in the prasinophyte alga Pseudoscourfieldia marina.Communications biology · 2026Article
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6 authors.
Funding
Abstract
The tiny green algae belonging to the class Chloropicophyceae play a key role in marine phytoplankton communities, especially in moderately oligotrophic water; yet, little is known about their biology, lifestyles, and what allows them to thrive in various oceanic environments. A single representative of this class (Chloropicon primus), comprising eight recognized species, has been previously subjected to genome analysis. To gain insight into the evolutionary changes that occurred during speciation in the Chloropicon genus and better understand the genes that distinguish Chloropicon species from other green algae traditionally designated as prasinophytes, we sequenced the genome of a second strain of C. primus and those of three strains of the closely related Chloropicon roscoffensis, the latter species representing the most dominant Chloropicon lineage in oceans. Our analyses highlighted substantial interspecific variations, including differences in chromosome number, gene content, gene arrangement, and ploidy state. Both C. primus genomes were predominantly diploid, while the C. roscoffensis genomes were either haploid or diploid. Specific proteins were identified for each species. Chloropicon roscoffensis possesses a biochemical C4-like inorganic carbon concentrating mechanism that potentially enables recycling of mitochondrial CO2 derived from photorespiration and respiration for carbon fixation in the chloroplast. In addition, it features specific proteins linked to the central carbon metabolism that suggest better coping mechanisms for abiotic stresses compared to C. primus. We also uncovered a previously undescribed eukaryotic recycling pathway for the micronutrient queuosine, a hypermodified nucleoside that is essential for post-transcriptional modification of several tRNAs at their anticodon wobble position.
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