Characterization of the c10orf76-PI4KB complex and its necessity for Golgi PI4P levels and enterovirus replication

EMBO Rep. 2020 Feb 5;21(2):e48441. doi: 10.15252/embr.201948441. Epub 2019 Dec 12.

Abstract

The lipid kinase PI4KB, which generates phosphatidylinositol 4-phosphate (PI4P), is a key enzyme in regulating membrane transport and is also hijacked by multiple picornaviruses to mediate viral replication. PI4KB can interact with multiple protein binding partners, which are differentially manipulated by picornaviruses to facilitate replication. The protein c10orf76 is a PI4KB-associated protein that increases PI4P levels at the Golgi and is essential for the viral replication of specific enteroviruses. We used hydrogen-deuterium exchange mass spectrometry to characterize the c10orf76-PI4KB complex and reveal that binding is mediated by the kinase linker of PI4KB, with formation of the heterodimeric complex modulated by PKA-dependent phosphorylation. Complex-disrupting mutations demonstrate that PI4KB is required for membrane recruitment of c10orf76 to the Golgi, and that an intact c10orf76-PI4KB complex is required for the replication of c10orf76-dependent enteroviruses. Intriguingly, c10orf76 also contributed to proper Arf1 activation at the Golgi, providing a putative mechanism for the c10orf76-dependent increase in PI4P levels at the Golgi.

Keywords: GBF1; HDX-MS; PI4KB; c10orf76; viral replication.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enterovirus* / genetics
  • Enterovirus* / metabolism
  • Golgi Apparatus / metabolism
  • Phosphatidylinositol Phosphates
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Protein Binding
  • Sf9 Cells
  • Virus Replication

Substances

  • Phosphatidylinositol Phosphates
  • Phosphotransferases (Alcohol Group Acceptor)