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DOI 10.1016/j.xgen.2026.101254

Медицинская библиотека · Cell genomics · 2026

A protein interactome for the last eukaryotic common ancestor illuminates the biochemical basis of modern genetic diseases.

Cox Rachael M, Papoulas Ophelia, Shril Shirlee, Lee Chanjae, Gardner Tynan P, Ansari Zoya T, Battenhouse Anna M, Lee Muyoung, Drew Kevin, McWhite Claire D, Yang David, Leggere Janelle C, Durand Dannie, Hildebrandt Friedhelm, Wallingford John B, Marcotte Edward M

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Аннотация

All eukaryotes share a single-celled ancestor from ∼1.5 to 1.8 billion years ago, the so-called last eukaryotic common ancestor (LECA). Roughly half of gene families found in modern eukaryotes were already present in LECA, forming molecular systems that continue to influence genetic diseases and traits today. To investigate these systems, we compared genes across 156 organisms to define a core set of protein-coding gene families likely present in LECA, with a quarter remaining uncharacterized. Integrating >26,000 mass spectrometry proteomics analyses from 31 species, we inferred higher-order complexes among these ancient proteins. This reconstructed interactome reveals both established and novel assemblies, offering a biochemical snapshot of LECA's organization. Finally, by exploring these ancient protein interactions, we found new human gene-disease associations for bone density and congenital birth defects, illustrating the value of ancestral protein networks for modern functional genetics.

Для цитирования: Cox Rachael M, Papoulas Ophelia, Shril Shirlee, Lee Chanjae, Gardner Tynan P, Ansari Zoya T, Battenhouse Anna M, Lee Muyoung, Drew Kevin, McWhite Claire D, Yang David, Leggere Janelle C, Durand Dannie, Hildebrandt Friedhelm, Wallingford John B, Marcotte Edward M. A protein interactome for the last eukaryotic common ancestor illuminates the biochemical basis of modern genetic diseases.. Cell genomics. 2026. DOI: 10.1016/j.xgen.2026.101254.

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