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

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Authors: Rachael M. Cox, Ophelia Papoulas, Shirlee Shril, Chanjae Lee, Tynan P Gardner, Zoya T. Ansari, Anna M. Battenhouse, Muyoung Lee, Kevin Drew, Claire D. McWhite, David Yang, Janelle C. Leggere
+4 more Dannie Durand, Friedhelm Hildebrandt, John B. Wallingford, Edward M. Marcotte
Cited by: 1
References: 178

Abstract

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.

Fields of Study & Subjects

Bioinformatics and Genomic Networks Genomics and Rare Diseases Digestive system and related health

Publication details

Journal / source
Cell Genomics
Publisher
Elsevier BV
Volume
6
Issue
6
Pages
101254–101254
Publication date
27 May 2026
Language
EN