首页> 外文期刊>The Journal of biological chemistry >Yeast Cells Lacking All Known Ceramide Synthases Continue to Make Complex Sphingolipids and to Incorporate Ceramides into Glycosylphosphatidylinositol (GPI) Anchors
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Yeast Cells Lacking All Known Ceramide Synthases Continue to Make Complex Sphingolipids and to Incorporate Ceramides into Glycosylphosphatidylinositol (GPI) Anchors

机译:缺乏所有已知的神经酰胺合成酶的酵母细胞继续制备复杂的鞘脂并将神经酰胺掺入糖基磷脂酰肌醇(GPI)锚固中

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In yeast, the inositolphosphorylceramides mostly contain C26:0 fatty acids. Inositolphosphorylceramides were considered to be important for viability because the inositolphosphorylceramide synthase AUR1 is essential. However, lcb1Δ cells, unable to make sphingoid bases and inositolphosphorylceramides, are viable if they harbor SLC1-1, a gain of function mutation in the 1-acyl-glycerol-3-phosphate acyltransferase SLC1. SLC1-1 allows the incorporation of C26:0 fatty acids into phosphatidylinositol (PI), thus generating PI″, an abnormal, C26-containing PI, presumably acting as surrogate for inositolphosphorylceramide. Here we show that the lethality of the simultaneous deletion of the known ceramide synthases LAG1/LAC1/LIP1 and YPC1/YDC1 can be rescued by the expression of SLC1-1 or the overexpression of AUR1. Moreover, lag1Δ lac1Δ ypc1Δ ydc1Δ (4Δ) quadruple mutants have been reported to be viable in certain genetic backgrounds but to still make some abnormal uncharacterized inositol-containing sphingolipids. Indeed, we find that 4Δ quadruple mutants make substantial amounts of unphysiological inositolphosphorylphytosphingosines but that they also still make small amounts of normal inositolphosphorylceramides. Moreover, 4Δ strains incorporate exogenously added sphingoid bases into inositolphosphorylceramides, indicating that these cells still possess an unknown pathway allowing the synthesis of ceramides. 4Δ cells also still add quite normal amounts of ceramides to glycosylphosphatidylinositol anchors. Synthesis of inositolphosphorylceramides and inositolphosphorylphytosphingosines is operated by Aur1p and is essential for growth of all 4Δ cells unless they contain SLC1-1. PI″, however, is made without the help of Aur1p. Furthermore, mannosylation of PI″ is required for the survival of sphingolipid-deficient strains, which depend on SLC1-1. In contrast to lcb1Δ SLC1-1, 4Δ SLC1-1 cells grow at 37 °C but remain thermosensitive at 44 °C.
机译:在酵母中,硅膦酸磷酰胺主要含有C26:0脂肪酸。由于碘磷磷酸化合成酶AUR1至关重要,硅膦磷酰胺被认为是重要的。然而,如果患有SLC1-1的SLC1-1,则LCB1δ细胞不能制备鞘氨酸碱基和氨基磷磷酸盐酰胺,是可行的,其在1-酰基 - 甘油-3-磷酸酰基酰基转移酶SLC1中的功能突变增益。 SLC1-1允许将C26:0脂肪酸掺入磷脂酰肌醇(PI),从而产生PI“,产生异常,C26的PI,可能是碘磷脂的替代物。在这里,我们表明,通过表达SLC1-1或AUR1的过表达,可以抵押同时缺失的同时缺失缺失的杀菌缺失的致死性。此外,据报道,LAG1ΔHAC1δYPC1δYDC1δ(4δ)四突变体在某些遗传背景中是可行的,但仍然制备一些异常的含含肌醇的鞘脂。实际上,我们发现4δ四重突变体制备大量的失药硅磷磷酸盐,但它们还仍然少量正常的硅膦酰胺。此外,4δ菌株将外源添加的鞘氨酸碱纳入碘磷酸化体中,表明这些细胞仍然具有允许合成神经酰胺的未知途径。 4Δ细胞还仍然将相当数量的酰胺加入糖基磷脂酰肌醇锚。通过AUR1P操作硅膦酰基团和碘磷虾的合成,除非它们含有SLC1-1,否则对于所有4δ细胞的生长至关重要。但是,在没有AUR1P的帮助下进行的“。此外,PI的甘露基化“是鞘脂缺乏菌株的存活所必需的,这取决于SLC1-1。与LCB1ΔSLC1-1,4ΔSLC1-1细胞相比,在37℃下生长,但在44℃下保持热敏。

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