No abstract

Cell polarisation is a fundamental biological process. Fission yeast is a key model system to study the molecular basis of microtubule-controlled cell polarisation. In this process, cells define prospective growth sites by generating distinct plasma membrane domains enriched in de novo synthesised sterols. Microtubules restrict the number and location of these domains by depositing factors at the cell poles. The mechanisms underlying such sterol-rich membrane domain formation and polarisation are largely unknown. We found that the oxysterol-binding proteins kes1p, osh2p and kes3p define three independent sterol delivery pathways to the plasma membrane. These mediate different phases of cell polarisation in a phosphoinositide-dependent fashion and differ in their requirement for vesicular trafficking steps. The redundant, kes1p- and osh2p-dependent pathways are vital and prime cell polarisation by mediating the formation of randomly distributed sterol-rich plasma membrane domains. Subsequent microtubule-controlled polarisation of these domains preferentially employs kes1p that directly delivers sterols to the plasma membrane independent of cdc42p. In cells lacking kes1p, polarisation becomes cdc42p-dependent, utilising mainly the kes3p-dependent pathway. Our study uncovers an essential biological function for non-vesicular lipid transport and establishes a molecular basis for different sterol-delivery pathways acting in cdc42p-independent and cdc42p-dependent cell polarisation.