REV7/FANCV Binds to CHAMP1 and Promotes Homologous Recombination Repair

Abstract

A critical determinant of DNA repair pathway choice is the HORMA protein REV7, a small abundant adaptor which binds to various DNA repair proteins through its C-terminal seatbelt domain. The REV7 seatbelt binds to the REV3 polymerase to form the Polymerase ζ complex, a positive regulator of translesion synthesis (TLS) repair. Alternatively, the REV7 seatbelt binds to SHLD3 in the Shieldin complex, a positive regulator of NHEJ repair. Recent studies have identified another novel REV7 seatbelt-binding protein, CHAMP1 (Chromosome Alignment-Maintaining Phosphoprotein 1), though its role in DNA repair is unknown. Here, we show that the REV7-CHAMP1 complex promotes homologous recombination (HR) repair by sequestering REV7 from the Shieldin complex. CHAMP1 competes directly with the SHLD3 subunit of the Shieldin complex for a limited pool of C-REV7, thereby inhibiting the REV7-mediated recruitment of the SHLD2 and SHLD1 effector subunits to DNA double-strand breaks. CHAMP1 thereby channels DNA repair away from error-prone NHEJ and towards the competing error-free HR pathway. Similarly, CHAMP1 competes with the REV3 component of the POL ζ complex, thereby reducing the level of mutagenic TLS repair. CHAMP1 interacts with POGZ in a heterochromatin complex further promoting HR repair. Importantly, in human tumors, CHAMP1 overexpression promotes HR, confers PARP inhibitor resistance, and correlates with poor prognosis. Thus, by binding to either REV3, SHLD3, or CHAMP1 through its seatbelt, the REV7 protein can promote either TLS repair, NHEJ repair, or HR repair respectively.

Biochemical characterization of human shieldin complex

“…A recent study suggests CHAMP1 along with REV7 is involved in DNA repair regulation. High levels of CHAMP1 favoured HR repair pathway in cells subjected to DNA DSBs using high doses of UV radiation (Li et al, 2021). Moreover, CHAMP1-REV7 complex formation is crucial for activation of HR pathway.…”

“…A recent study identified a conserved Threonine at position 103 to be target for phosphorylation (Li et al, 2021). Moreover, the phosphorylated form of REV7 was enriched in the chromatin bound fractions as opposed to nonchromatin bound fractions.…”