Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Department of Microbiology and Immunology, Stony Brook University, Stony Brook, NY, USA.
Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Sep;1866(9):158983. doi: 10.1016/j.bbalip.2021.158983. Epub 2021 May 29.
SBF (Swi4/Swi6 Binding Factor) complex is a crucial regulator of G1/S transition in Saccharomyces cerevisiae. Here, we show that SBF complex is required for myriocin resistance, an inhibitor of sphingolipid synthesis. This phenotype was not shared with MBF complex mutants nor with deletion of the Swi4p downstream targets, CLN1/CLN2. Based on data mining results, we selected putative Swi4p targets related to sphingolipid metabolism and studied their gene transcription as well as metabolite levels during progression of the cell cycle. Genes which encode key enzymes for the synthesis of long chain bases (LCBs) and ceramides were periodically transcribed during the mitotic cell cycle, having a peak at G1/S, and required SWI4 for full transcription at this stage. In addition, HPLC-MS/MS data indicated that swi4Δ cells have decreased levels of sphingolipids during progression of the cell cycle, particularly, dihydrosphingosine (DHS), C24-phytoceramides and C24-inositolphosphoryl ceramide (IPC) while it had increased levels of mannosylinositol phosphorylceramide (MIPC). Furthermore, we demonstrated that both inhibition of de novo sphingolipid synthesis by myriocin or SWI4 deletion caused partial arrest at the G2/M phase. Importantly, our lipidomic data demonstrated that the sphingolipid profile of WT cells treated with myriocin resembled that of swi4Δ cells, with lower levels of DHS, IPC and higher levels of MIPC. Taken together, these results show that SBF complex plays an essential role in the regulation of sphingolipid homeostasis, which reflects in the correct progression through the G2/M phase of the cell cycle.
SBF(Swi4/Swi6 结合因子)复合物是酿酒酵母 G1/S 转换的关键调节因子。在这里,我们表明 SBF 复合物是麦角甾醇合成抑制剂(myriocin)抗性所必需的。这种表型与 MBF 复合物突变体或 Swi4p 下游靶标 CLN1/CLN2 的缺失不同。基于数据挖掘结果,我们选择了与鞘脂代谢相关的假定 Swi4p 靶标,并研究了它们在细胞周期进展过程中的基因转录和代谢物水平。编码长链碱基 (LCB) 和神经酰胺合成关键酶的基因在有丝分裂细胞周期中周期性转录,在 G1/S 时达到峰值,并且在这个阶段需要 SWI4 进行完全转录。此外,HPLC-MS/MS 数据表明,swi4Δ 细胞在细胞周期进展过程中鞘脂水平降低,特别是二氢神经鞘氨醇 (DHS)、C24-植物神经酰胺和 C24-肌醇磷酸神经酰胺 (IPC),而它们的甘露糖基肌醇磷酸神经酰胺 (MIPC)水平升高。此外,我们证明了麦角甾醇合成的从头抑制(myriocin)或 SWI4 缺失都会导致细胞在 G2/M 期部分停滞。重要的是,我们的脂质组学数据表明,用麦角甾醇处理的 WT 细胞的鞘脂谱类似于 swi4Δ 细胞,DHS、IPC 水平降低,MIPC 水平升高。总之,这些结果表明 SBF 复合物在调节鞘脂动态平衡中起着至关重要的作用,这反映在细胞周期 G2/M 期的正确进展中。