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Updated: Jul 6, 2026

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
Published on: May 2, 2025
Early evolution of eukaryotic DNA-dependent RNA polymerases
Marta Kwapisz1, Frédéric Beckouët, Pierre Thuriaux
1CEA, iBiTec-S, Service de Biologie Intégrative et Génétique Moléculaire, Gif-sur-Yvette F-91191, France.
Eukaryotic RNA polymerases share a conserved core with archaeal enzymes. The Rpb8 subunit, previously thought eukaryotic, is structurally similar to archaeal protein G, linking these polymerase structures.
Area of Science:
- Molecular Biology
- Biochemistry
- Evolutionary Biology
Background:
- Eukaryotic DNA-dependent RNA polymerases (Pol I-III) possess a conserved 12-subunit core structure.
- This core structure shows significant homology to archaeal RNA polymerases.
- The Rpb8 subunit was traditionally considered exclusive to eukaryotic RNA polymerases.
Purpose of the Study:
- To investigate the evolutionary origins and structural relationships of eukaryotic RNA polymerase subunits.
- To determine if the Rpb8 subunit has homologs in archaeal organisms.
- To identify potential missing links in the evolution of archaeal and eukaryotic RNA polymerases.
Main Methods:
- Comparative structural analysis of protein sequences.
- Bioinformatic analysis of archaeal and eukaryotic RNA polymerase subunits.
- Phylogenetic analysis to infer evolutionary relationships.
Main Results:
- The eukaryotic Rpb8 subunit shares significant structural resemblance to an archaeal protein, designated protein G.
- Protein G is exclusively found in the Crenarchaea archaeal phylum.
- This finding establishes a direct link between the core structures of archaeal and eukaryotic RNA polymerases.
Conclusions:
- The Rpb8 subunit is not exclusive to eukaryotes and has an archaeal origin.
- The discovery of protein G as an Rpb8 homolog bridges a gap in understanding RNA polymerase evolution.
- This research provides critical insights into the conserved mechanisms of transcription across different domains of life.
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