Universitätsklinikum Münster, Klinik und Poliklinik für Kinder- und Jugendmedizin-Allgemeine Pädiatrie, Münster, Germany.
Mol Genet Metab. 2012 Apr;105(4):642-51. doi: 10.1016/j.ymgme.2011.12.017. Epub 2011 Dec 29.
Congenital disorders of glycosylation (CDG) are caused by a dysfunction of glycosylation, an essential step in the manufacturing process of glycoproteins. This paper focuses on a 6-year-old patient with a new type of CDG-I caused by a defect of the steroid 5α reductase type 3 gene (SRD5A3). The clinical features were psychomotor retardation, pathological nystagmus, slight muscular hypotonia and microcephaly. SRD5A3 was recently identified encoding the polyprenol reductase, an enzyme catalyzing the final step of the biosynthesis of dolichol, which is required for the assembly of the glycans needed for N-glycosylation. Although an early homozygous stop-codon (c.57G>A [W19X]) with no functional protein was found in the patient, about 70% of transferrin (Tf) was correctly glycosylated. Quantification of dolichol and unreduced polyprenol in the patient's fibroblasts demonstrated a high polyprenol/dolichol ratio with normal amounts of dolichol, indicating that high polyprenol levels might compete with dolichol for the initiation of N-glycan assembly but without supporting normal glycosylation and that there must be an alternative pathway for dolichol biosynthesis.
先天性糖基化障碍(CDG)是由糖基化功能障碍引起的,糖基化是糖蛋白制造过程中的一个必要步骤。本文重点介绍了一名 6 岁的新类型 CDG-I 患者,其病因是类固醇 5α 还原酶 3 型基因(SRD5A3)缺陷。临床表现为精神运动发育迟缓、病理性眼球震颤、轻度肌肉张力减退和小头畸形。SRD5A3 最近被鉴定为多萜醇还原酶的编码基因,该酶催化多萜醇生物合成的最后一步,多萜醇是 N-糖基化所需聚糖组装所必需的。尽管在患者中发现了一个早期的纯合无义突变(c.57G>A [W19X]),没有功能性蛋白,但约 70%的转铁蛋白(Tf)被正确糖基化。患者成纤维细胞中多萜醇和未还原多萜的定量分析显示多萜醇/多萜醇比值高,多萜醇正常,表明高多萜醇水平可能与多萜醇竞争 N-聚糖组装的起始,但不支持正常糖基化,并且必须存在多萜醇生物合成的替代途径。