Intracellular Trafficking Pathway of Yeast Long-chain Base Kinase Lcb4, from Its Synthesis to Its Degradation

• Published in: The Journal of biological chemistry 2007-09, Vol.282 (39), p.28485-28492
• Main Authors: Iwaki, Soichiro, Sano, Takamitsu, Takagi, Tomoko, Osumi, Masako, Kihara, Akio, Igarashi, Yasuyuki
• Format: Article
• Language: English
• Subjects: Cell Membrane - enzymology; Cell Membrane - ultrastructure; Endoplasmic Reticulum - enzymology; Endoplasmic Reticulum - ultrastructure; G1 Phase - physiology; Golgi Apparatus - enzymology; Golgi Apparatus - ultrastructure; Lysophospholipids - metabolism; Nuclear Envelope - enzymology; Nuclear Envelope - ultrastructure; Palmitic Acid - metabolism; Phosphorylation; Phosphotransferases (Alcohol Group Acceptor) - metabolism; Protein Processing, Post-Translational - physiology; Protein Transport - physiology; Saccharomyces cerevisiae; Saccharomyces cerevisiae - enzymology; Saccharomyces cerevisiae - ultrastructure; Saccharomyces cerevisiae Proteins - metabolism; Sphingosine - analogs & derivatives; Sphingosine - metabolism; Vacuoles - enzymology; Vacuoles - ultrastructure
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M701607200

Sphingoid long-chain base 1-phosphates act as bioactive lipid molecules in eukaryotic cells. In budding yeast, long-chain base 1-phosphates are synthesized mainly by the long-chain base kinase Lcb4. We recently reported that, soon after yeast cells enter into the stationary phase, Lcb4 is rapidly degraded by being delivered to the vacuole in a palmitoylation- and phosphorylation-dependent manner. In this study, we investigated the complete trafficking pathway of Lcb4, from its synthesis to its degradation. After membrane anchoring by palmitoylation at the Golgi apparatus, Lcb4 is delivered to the plasma membrane (PM) through the late Sec pathway and then to the endoplasmic reticulum (ER). The yeast ER consists of a cortical network juxtaposed to the PM (cortical ER) with tubular connections to the nuclear envelope (nuclear ER). Remarkably, the localization of Lcb4 is restricted to the cortical ER. As the cells reach the stationary phase, G1 cell cycle arrest initiates Lcb4 degradation and its delivery to the vacuole via the Golgi apparatus. The protein transport pathway from the PM to the ER found in this study has not been previously reported. We speculate that this novel pathway is mediated by the PM-ER contact.