Structural basis for the assembly of the DNA polymerase holoenzyme from a monkeypox virus variant

The ongoing global pandemic caused by a variant of the monkeypox (or mpox) virus (MPXV) has prompted widespread concern. The MPXV DNA polymerase holoenzyme, consisting of F8, A22, and E4, is vital for repli-cating the viral genome and represents a crucial target for the development of antiviral drugs. However, the assembly and working mechanism for the DNA polymerase holoenzyme of MPXV remains elusive. Here, we present the cryo-electron microscopy (cryo-EM) structure of the DNA polymerase holoenzyme at an overall res-olution of 3.5 A. Unexpectedly, the holoenzyme is assembled as a dimer of heterotrimers, of which the extra interface between the thumb domain of F8 and A22 shows a clash between A22 and substrate DNA, suggesting an autoinhibition state. Addition of exogenous double-stranded DNA shifts the hexamer into trimer exposing DNA binding sites, potentially representing a more active state. Our findings provide crucial steps toward de-veloping targeted antiviral therapies for MPXV and related viruses.

Automated summary

The ongoing global pandemic caused by a variant of the monkeypox virus has raised concerns. The structure and mechanism of the DNA polymerase holoenzyme of the virus remains elusive, but recent research has provided insights into its assembly and functioning. These findings are important for developing targeted antiviral therapies.