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佩利措伊斯-梅茨巴赫病:髓磷脂蛋白脂质基因中的移码缺失/插入事件。

Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene.

作者信息

Pham-Dinh D, Boespflug-Tanguy O, Mimault C, Cavagna A, Giraud G, Leberre G, Lemarec B, Dautigny A

机构信息

Equipe ATIPE, URA 1488 CNRS, Paris, France.

出版信息

Hum Mol Genet. 1993 Apr;2(4):465-7. doi: 10.1093/hmg/2.4.465.

Abstract

Among the central nervous system (CNS) dysmyelinating disorders, Pelizaeus-Merzbacher disease (PMD) has been individualized by its X-linked mode of inheritance and the existence of corresponding animal models. Mutations in the major myelin proteolipid (PLP) gene coding for PLP and its splicing variant DM20 protein, have been demonstrated in animal mutants and more recently in PMD affected patients. We have identified, in a two-generation PMD affected family, an insertion/deletion event in the exon IV of the PLP gene, leading to the synthesis of predicted truncated PLP and DM20 proteins with altered carboxyl terminal end. This is the first report of a frameshift mutation in the PLP gene in PMD.

摘要

在中枢神经系统(CNS)脱髓鞘疾病中,佩利措伊斯-梅茨巴赫病(PMD)因其X连锁遗传模式和相应动物模型的存在而具有独特性。编码髓鞘蛋白脂蛋白(PLP)及其剪接变体DM20蛋白的主要髓鞘蛋白脂蛋白(PLP)基因突变,已在动物突变体中得到证实,最近在受PMD影响的患者中也得到证实。我们在一个两代受PMD影响的家族中,发现了PLP基因外显子IV中的一个插入/缺失事件,导致合成了预测的截短型PLP和羧基末端改变的DM20蛋白。这是PMD中PLP基因移码突变的首次报道。

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