一个OGT错觉变体与严重发育迟缓和肝细胞瘤的儿童中受损的酶活性
Alfonso Manuel D'Alessio1,2,3, Huijie Yuan4,5, Leandro Raul Soria1
1Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
American journal of medical genetics. Part A
|October 1, 2025
概括
一种新的O-GlcNAc转移酶 (OGT) 基因变异在患有发育迟缓和肝细胞瘤的儿童中引起了OGT-CDG. 这一发现表明,OGT缺乏和癌症风险之间存在潜在的联系.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- O-GlcNAc转移酶 (OGT) 和O-GlcNAcase (OGA) 调节O-GlcNAcylation,这是代谢传感中的一个关键的翻译后修改.
- 致病性OGT变异导致X链接的血糖化先天性障碍 (OGT-CDG),其特点是发育迟缓,低血压,智力障碍和异形特征.
研究的目的:
- 在患有OGT-CDG和肝细胞瘤的儿童中报告一种新的OGT变异.
- 调查已识别的OGT变异的功能影响.
主要方法:
- 异位序列测序以识别OGT变种.
- 西方斑点分析患者衍生纤维细胞.
- 在体外酶活性测定.
主要成果:
- 在一个患有发育迟缓,低血压,异形特征和肝细胞瘤的儿童身上发现了一种新的误解性OGT变体.
- 来自患者的纤维细胞显示O-GlcNAcylation和OGA表达的减少.
- 该变种在体外显著降低了OGT酶活性,证实了病原性.
结论:
- 这一病例扩大了OGT-CDG的临床表型,包括肝细胞瘤.
- 这些发现表明,OGT缺乏与癌症风险增加之间存在潜在的关联,需要进一步调查.
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