A Lipid Transfer Protein Signaling Axis Exerts Dual Control of Cell-Cycle and Membrane Trafficking Systems. Academic Article uri icon

abstract

  • Kes1/Osh4 is a member of the conserved, but functionally enigmatic, oxysterol binding protein-related protein (ORP) superfamily that inhibits phosphatidylinositol transfer protein (Sec14)-dependent membrane trafficking through the trans-Golgi (TGN)/endosomal network. We now report that Kes1, and select other ORPs, execute cell-cycle control activities as functionally non-redundant inhibitors of the G1/S transition when cells confront nutrient-poor environments and promote replicative aging. Kes1-dependent cell-cycle regulation requires the Greatwall/MASTL kinase ortholog Rim15, and is opposed by Sec14 activity in a mechanism independent of Kes1/Sec14 bulk membrane-trafficking functions. Moreover, the data identify Kes1 as a non-histone target for NuA4 through which this lysine acetyltransferase co-modulates membrane-trafficking and cell-cycle activities. We propose the Sec14/Kes1 lipid-exchange protein pair constitutes part of the mechanism for integrating TGN/endosomal lipid signaling with cell-cycle progression and hypothesize that ORPs define a family of stage-specific cell-cycle control factors that execute tumor-suppressor-like functions.

published proceedings

  • Dev Cell

altmetric score

  • 5

author list (cited authors)

  • Huang, J., Mousley, C. J., Dacquay, L., Maitra, N., Drin, G., He, C., ... Bankaitis, V. A

citation count

  • 28

complete list of authors

  • Huang, Jin||Mousley, Carl J||Dacquay, Louis||Maitra, Nairita||Drin, Guillaume||He, Chong||Ridgway, Neale D||Tripathi, Ashutosh||Kennedy, Michael||Kennedy, Brian K||Liu, Wenshe||Baetz, Kristin||Polymenis, Michael||Bankaitis, Vytas A

publication date

  • February 2018