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Vol 60(2026) N 4 p. 514-522; DOI 10.1134/S0026893326700056 Full Text

E.S. Egorov1, M.S. Gelfand2,3, I.V. Zhegalova4*

Enhancer-like Elements and Evolutionary Age of Dictyostelium discoideum Genes: Association with Stage Activity

1Faculty of Bioengineering and Bioinformatics, Moscow State University, Moscow, 119991 Russia
2Skolkovo Institute of Science and Technology, Moscow, 121205 Russia
3Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, 119991 Russia
4Institute of Gene Biology, Russian Academy of Sciences, Moscow, 119334 Russia


*ir.zhegalova@gmail.com
Received - 2025-10-28; Revised - 2025-12-05; Accepted - 2026-01-26

The development of the social amoeba Dictyostelium discoideum provides a convenient model for studying the transition from a unicellular to a multicellular state and the accompanying changes in gene expression regulation. The evolutionary age of genes and the activity of enhancer-like elements (ELEs) were comparatively analyzed at four stages of the amoeba life cycle: vegetative, streaming, mound, and fruiting. Calculation of the transcriptomic age index (TAI) showed that the relative contribution of evolutionarily young genes increases during the transition to multicellularity, while ancient genes maintain a high level of expression throughout the entire developmental cycle. Genes associated with ELEs were found to be evolutionarily more ancient and, on average, longer due to the greater length of the coding sequence, with a lower density of introns per gene. Changes in ELE accessibility were most often accompanied by a decrease in expression of neighbor genes, especially within 10 kb, while the total number of identified elements strongly depended on the sequencing depth. The results indicate a combination of a conservative set of ancient enhancer-associated genes with selective activation of young, stage-dependent transcripts at the late stages of D. discoideum development.

gene regulation, enhancers, evolutionary age, transcriptomic age index, Dictyostelium discoideum, multicellularity, chromatin accessibility



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