Dwyer Chrissa A, Esko Jeffrey D
Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California, San Diego, La Jolla, CA 92093, USA.
Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California, San Diego, La Jolla, CA 92093, USA.
Mol Aspects Med. 2016 Oct;51:104-14. doi: 10.1016/j.mam.2016.07.001. Epub 2016 Jul 11.
Idiopathic autism spectrum disorders (ASDs) are neurodevelopmental disorders with unknown etiology. An estimated 1:68 children in the U.S. are diagnosed with ASDs, making these disorders a substantial public health issue. Recent advances in genome sequencing have identified numerous genetic variants across the ASD patient population. Many genetic variants identified occur in genes that encode glycosylated extracellular proteins (proteoglycans or glycoproteins) or enzymes involved in glycosylation (glycosyltransferases and sulfotransferases). It remains unknown whether "glycogene" variants cause changes in glycosylation and whether they contribute to the etiology and pathogenesis of ASDs. Insights into glycan susceptibility factors are provided by studies in the normal brain and congenital disorders of glycosylation, which are often accompanied by ASD-like behaviors. The purpose of this review is to present evidence that supports a contribution of extracellular glycans and glycoconjugates to the etiology and pathogenesis of idiopathic ASDs and other types of pervasive neurodevelopmental disorders.
特发性自闭症谱系障碍(ASD)是病因不明的神经发育障碍。据估计,美国每68名儿童中就有1名被诊断患有ASD,这使这些疾病成为一个重大的公共卫生问题。基因组测序的最新进展已在ASD患者群体中鉴定出众多基因变异。所鉴定出的许多基因变异发生在编码糖基化细胞外蛋白(蛋白聚糖或糖蛋白)或参与糖基化的酶(糖基转移酶和磺基转移酶)的基因中。“糖基因”变异是否会导致糖基化变化以及它们是否促成ASD的病因和发病机制仍不清楚。对正常大脑和糖基化先天性疾病的研究提供了对聚糖易感性因素的见解,这些疾病常伴有ASD样行为。本综述的目的是提供证据,支持细胞外聚糖和糖缀合物对特发性ASD及其他类型广泛性神经发育障碍的病因和发病机制的作用。