Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
J Biol Chem. 2023 Aug;299(8):105016. doi: 10.1016/j.jbc.2023.105016. Epub 2023 Jul 5.
The biosynthesis of glycosylphosphatidylinositol (GPI)-anchored proteins (GPI-APs) in the parasitic protozoan Trypanosoma brucei involves fatty acid remodeling of the GPI precursor molecules before they are transferred to protein in the endoplasmic reticulum. The genes encoding the requisite phospholipase A2 and A1 activities for this remodeling have thus far been elusive. Here, we identify a gene, Tb927.7.6110, that encodes a protein that is both necessary and sufficient for GPI-phospholipase A2 (GPI-PLA2) activity in the procyclic form of the parasite. The predicted protein product belongs to the alkaline ceramidase, PAQR receptor, Per1, SID-1, and TMEM8 (CREST) superfamily of transmembrane hydrolase proteins and shows sequence similarity to Post-GPI-Attachment to Protein 6 (PGAP6), a GPI-PLA2 that acts after transfer of GPI precursors to protein in mammalian cells. We show the trypanosome Tb927.7.6110 GPI-PLA2 gene resides in a locus with two closely related genes Tb927.7.6150 and Tb927.7.6170, one of which (Tb927.7.6150) most likely encodes a catalytically inactive protein. The absence of GPI-PLA2 in the null mutant procyclic cells not only affected fatty acid remodeling but also reduced GPI anchor sidechain size on mature GPI-anchored procyclin glycoproteins. This reduction in GPI anchor sidechain size was reversed upon the re-addition of Tb927.7.6110 and of Tb927.7.6170, despite the latter not encoding GPI precursor GPI-PLA2 activity. Taken together, we conclude that Tb927.7.6110 encodes the GPI-PLA2 of GPI precursor fatty acid remodeling and that more work is required to assess the roles and essentiality of Tb927.7.6170 and the presumably enzymatically inactive Tb927.7.6150.
在寄生原生动物布氏锥虫中,糖基磷脂酰肌醇 (GPI)-锚定蛋白 (GPI-APs) 的生物合成涉及 GPI 前体分子在被转移到内质网中的蛋白质之前的脂肪酸重塑。因此,编码这种重塑所需的磷脂酶 A2 和 A1 活性的基因一直难以捉摸。在这里,我们鉴定了一个基因 Tb927.7.6110,该基因编码的蛋白质对于寄生虫前鞭毛体形式的 GPI-磷脂酶 A2 (GPI-PLA2) 活性是必需且充分的。预测的蛋白产物属于碱性神经酰胺酶、PAQR 受体、Per1、SID-1 和 TMEM8(CREST)跨膜水解酶蛋白超家族,并与哺乳动物细胞中 GPI 前体转移到蛋白质后起作用的 GPI-PLA2(PGAP6)具有序列相似性。我们表明,锥虫 Tb927.7.6110 GPI-PLA2 基因位于一个与两个密切相关的基因 Tb927.7.6150 和 Tb927.7.6170 相关的基因座中,其中一个(Tb927.7.6150)很可能编码一种无催化活性的蛋白质。在缺失突变体前鞭毛体细胞中缺乏 GPI-PLA2 不仅影响脂肪酸重塑,还降低了成熟 GPI-锚定前鞭毛蛋白糖蛋白上的 GPI 锚定侧链大小。这种 GPI 锚定侧链大小的减少在 Tb927.7.6110 和 Tb927.7.6170 的重新添加时得到逆转,尽管后者不编码 GPI 前体 GPI-PLA2 活性。总之,我们得出结论,Tb927.7.6110 编码 GPI 前体脂肪酸重塑的 GPI-PLA2,需要进一步研究以评估 Tb927.7.6170 和假定无酶活性的 Tb927.7.6150 的作用和必要性。