Cell GenomicsEvolutionary BiologyPeer-reviewed journal article
A protein interactome for the last eukaryotic common ancestor illuminates the biochemical basis of modern genetic diseases
Rachael M. CoxiD, Ophelia PapoulasiD, Shirlee ShriliD, Chanjae LeeiD, Tynan P. GardneriD, Zoya T. AnsariiD, Anna M. BattenhouseiD, Muyoung LeeiD, Kevin DrewiD, Claire D. McWhiteiD, David Yang, Janelle C. LeggereiD, Dannie DurandiD, Friedhelm HildebrandtiD, John B. WallingfordiD, Edward M. MarcotteiD
Abstract
All eukaryotes share a single-celled ancestor from [~]1.5-1.8 billion years ago, the 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 LECAs 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.
- organism: multiple species
- assay: proteomics
- research focus: cell type annotation
- research focus: gene regulatory network inference
- approach: experimental assay
- Citations
- 5
- FWCI
- 5.84
- Field percentile
- top 3%
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