Vogt Guillaume, Vogt Benoît, Chuzhanova Nadia, Julenius Karin, Cooper David N, Casanova Jean-Laurent
Laboratory of Human Genetics of Infectious Diseases, INSERM, U550, Paris 75015, France.
Curr Opin Genet Dev. 2007 Jun;17(3):245-51. doi: 10.1016/j.gde.2007.04.008. Epub 2007 Apr 30.
Disease-causing missense (and other in-frame) mutations can exert their deleterious effects at the cellular level through multiple mechanisms. A pathogenic mechanism involves the addition of a novel N-linked glycan. Up to 1.4% of known disease-causing missense mutations are predicted to give rise to gains-of-glycosylation. For some of these mutations, the novel glycans have been shown to be both necessary and sufficient to account for the deleterious impact of the mutation. The chemical complementation of cells from patients in vitro with various modifiers of glycosylation has been demonstrated and raises the possibility of specific chemical treatments for patients bearing gain-of-glycosylation mutations.
导致疾病的错义(以及其他框内)突变可通过多种机制在细胞水平发挥其有害作用。一种致病机制涉及添加新的N-连接聚糖。据预测,高达1.4%的已知致病错义突变会导致糖基化增加。对于其中一些突变,已证明新的聚糖对于解释突变的有害影响既必要又充分。体外对患者细胞与各种糖基化修饰剂进行化学互补已得到证实,这增加了对携带糖基化增加突变的患者进行特异性化学治疗的可能性。