The Human Primosome Requires Replication Protein A When Copying DNA with Inverted Repeats

Authors

Andrey G. Baranovskiy, University of Nebraska Medical Center
Lucia M. Morstadt, University of Nebraska Medical Center
Eduardo E. Romero, University of Nebraska-Lincoln
Nigar D. Babayeva, University of Nebraska Medical Center
Tahir H. Tahirov, University of Nebraska Medical CenterFollow

ORCID IDs

Tahirov https://orcid.org/0000-0002-1238-0069

Document Type

Article

Date of this Version

2025

Citation

Nucleic Acids Research (2025) 53(15): gkaf799

Comments

Open access

License: CC BY-NC 4.0

Abstract

The human primosome, a four-subunit complex of primase and DNA polymerase alpha (Polα), initiates DNA synthesis on both chromosome strands by generating chimeric RNA–DNA primers for loading DNA polymerases delta and epsilon (Polϵ). Replication protein A (RPA) tightly binds to single-stranded DNA strands, protecting them from nucleolytic digestion and unauthorized transactions. We report here that RPA plays a critical role for the human primosome during DNA synthesis across inverted repeats prone to hairpin formation. On other alternatively structured DNA, forming a G-quadruplex, RPA does not assist primosome. A stimulatory effect of RPA on DNA synthesis across hairpins was also observed for the catalytic domain of Polα but not of Polϵ. The winged helix-turn-helix domain of RPA is essential for an efficient hairpin bypass and increases RPA–Polα cooperativity on the primed DNA template. Cryo-EM studies revealed that this domain is mainly responsible for the interaction between RPA and Polα. The flexible mode of RPA–Polα interaction during DNA synthesis implies the mechanism of template handover between them when the hairpin formation should be avoided. This work provides insight into a cooperative action of RPA and primosome on DNA, which is critical for DNA synthesis across inverted repeats.