APE1 recruits ATRIP to ssDNA in an RPA-independent manner to promote the ATR DNA damage response

Cells have evolved the DNA damage response (DDR) pathways in response to DNA replication stress or DNA damage. In the ATR-Chk1 DDR pathway, it has been proposed that ATR is recruited to RPA-coated single-strand DNA (ssDNA) by direct ATRIP-RPA interaction. However, it remains elusive whether and how ATRIP is recruited to ssDNA in an RPA-independent manner. Here, we provide evidence that APE1 directly associates ssDNA to recruit ATRIP onto ssDNA in an RPA-independent fashion. The N-terminal motif within APE1 is required and sufficient for the APE1-ATRIP interaction in vitro and the distinct APE1-ATRIP interaction is required for ATRIP recruitment to ssDNA and the ATR-Chk1 DDR pathway activation in Xenopus egg extracts. In addition, APE1 directly associates with RPA70 and RPA32 via two distinct motifs. Taken together, our evidence identifies APE1 as a direct recruiter of ATRIP onto ssDNA independent of RPA in the activation of ATR DDR pathway. SummaryO_LIAPE1 associates with ssDNA and ATRIP directly via distinct motifs and thereby recruits ATRIP onto ssDNA independent of RPA to promote the ATR DDR. C_LIO_LIAPE1 interacts with RPA via distinct two motifs in vitro but such RPA-APE1 interaction is dispensable for ATRIP recruitment onto ssDNA. C_LI