Protzer C E, Preiss A, Nagel A C
Universität Hohenheim, Institut für Genetik (240), Garbenstrasse 30, 70599, Stuttgart, Germany.
Cell Tissue Res. 2009 Apr;336(1):149-58. doi: 10.1007/s00441-009-0758-1. Epub 2009 Feb 28.
In a genetic screen, alpha-4GT1 has been identified as a potential enhancer of Hairless-mediated cell death in the eye of Drosophila. alpha-4GT1 encodes an alpha-1,4-glycosyltransferase, known to catalyze the fifth step in a series of ceramide glycosylation events. As reported for other enzymes involved in the glycosylation of ceramide, alpha-4GT1 is strongly expressed during oogenesis and is deposited maternally in the egg. Moreover, the protein is enriched at cell membranes. Unexpectedly, overexpression of alpha-4GT1 does not enhance Hairless-mediated cell death; instead, Hairless enhancement is caused by an allele of Scutoid present on the alpha-4GT1 chromosome. Interestingly, the downregulation of alpha-4GT1 during eye development amplifies cell death induction by the pro-apoptotic gene reaper. Accordingly, overexpression of alpha-4GT1 represses reaper-induced cell death. Thus, alpha-4GT1 appears to be an inhibitor of apoptosis, as has previously been observed for other ceramide glycosylating enzymes, suggesting that it likewise contributes to ceramide anchoring in the membrane.
在一项基因筛选中,α-4GT1已被鉴定为果蝇眼中无毛介导的细胞死亡的潜在增强子。α-4GT1编码一种α-1,4-糖基转移酶,已知该酶催化一系列神经酰胺糖基化事件中的第五步。正如报道的参与神经酰胺糖基化的其他酶一样,α-4GT1在卵子发生过程中强烈表达,并通过母体沉积在卵子中。此外,该蛋白在细胞膜上富集。出乎意料的是,α-4GT1的过表达并未增强无毛介导的细胞死亡;相反,无毛增强是由α-4GT1染色体上存在的类盾形基因的一个等位基因引起的。有趣的是,在眼睛发育过程中α-4GT1的下调会放大促凋亡基因收割者诱导的细胞死亡。因此,α-4GT1的过表达会抑制收割者诱导的细胞死亡。因此,α-4GT1似乎是一种凋亡抑制剂,正如之前在其他神经酰胺糖基化酶中观察到的那样,这表明它同样有助于神经酰胺锚定在膜中。