Suppr超能文献

自闭症谱系障碍中的聚糖易感性因素。

Glycan susceptibility factors in autism spectrum disorders.

作者信息

Dwyer Chrissa A, Esko Jeffrey D

机构信息

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.

出版信息

Mol Aspects Med. 2016 Oct;51:104-14. doi: 10.1016/j.mam.2016.07.001. Epub 2016 Jul 11.

Abstract

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.

摘要

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。

相似文献

1
Glycan susceptibility factors in autism spectrum disorders.
Mol Aspects Med. 2016 Oct;51:104-14. doi: 10.1016/j.mam.2016.07.001. Epub 2016 Jul 11.
3
Molecular Functions of Glycoconjugates in Autophagy.
J Mol Biol. 2016 Aug 14;428(16):3305-3324. doi: 10.1016/j.jmb.2016.06.011. Epub 2016 Jun 23.
4
Distortion of the normal function of synaptic cell adhesion molecules by genetic variants as a risk for autism spectrum disorders.
Brain Res Bull. 2017 Mar;129:82-90. doi: 10.1016/j.brainresbull.2016.10.006. Epub 2016 Oct 12.
5
ERK/MAPK signaling and autism spectrum disorders.
Prog Brain Res. 2018;241:63-112. doi: 10.1016/bs.pbr.2018.09.008. Epub 2018 Nov 1.
6
Preface.
Methods Enzymol. 2017;597:xv-xix. doi: 10.1016/S0076-6879(17)30318-X.
7
How glycosylation affects glycosylation: the role of N-glycans in glycosyltransferase activity.
Glycobiology. 2020 Dec 9;30(12):941-969. doi: 10.1093/glycob/cwaa041.
8
Exploring glycans as vital biological macromolecules: A comprehensive review of advancements in biomedical frontiers.
Int J Biol Macromol. 2024 May;268(Pt 1):131511. doi: 10.1016/j.ijbiomac.2024.131511. Epub 2024 Apr 13.
9
[Role of NRXN-NLGN-SHANK pathway gene variations in the pathogenesis of autism spectrum disorders].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):753-756. doi: 10.3760/cma.j.issn.1003-9406.2018.05.031.
10
Variation in Gene Expression in Autism Spectrum Disorders: An Extensive Review of Transcriptomic Studies.
Front Neurosci. 2017 Jan 5;10:601. doi: 10.3389/fnins.2016.00601. eCollection 2016.

引用本文的文献

1
MAN2A2-related glycosylation defects in autism and cognitive delay.
Sci Rep. 2025 Jul 8;15(1):24471. doi: 10.1038/s41598-025-09400-5.
3
4
Efficacy of sialic acid supplementation in early life in autism model rats.
Sci Rep. 2025 Mar 12;15(1):8576. doi: 10.1038/s41598-025-93550-z.
5
Glycosylation Pathways Targeted by Deregulated miRNAs in Autism Spectrum Disorder.
Int J Mol Sci. 2025 Jan 17;26(2):783. doi: 10.3390/ijms26020783.
6
Clinical glycoproteomics: methods and diseases.
MedComm (2020). 2024 Oct 4;5(10):e760. doi: 10.1002/mco2.760. eCollection 2024 Oct.
9
Sex-specific DNA methylation signatures of autism spectrum disorder in newborn blood.
bioRxiv. 2024 Dec 2:2024.07.11.603098. doi: 10.1101/2024.07.11.603098.
10

本文引用的文献

1
Relevance of Neuroinflammation and Encephalitis in Autism.
Front Cell Neurosci. 2016 Jan 19;9:519. doi: 10.3389/fncel.2015.00519. eCollection 2015.
2
Modulation of Cav3.2 T-type calcium channel permeability by asparagine-linked glycosylation.
Channels (Austin). 2016;10(3):175-84. doi: 10.1080/19336950.2016.1138189. Epub 2016 Jan 8.
3
Expanding the 3-O-Sulfate Proteome--Enhanced Binding of Neuropilin-1 to 3-O-Sulfated Heparan Sulfate Modulates Its Activity.
ACS Chem Biol. 2016 Apr 15;11(4):971-80. doi: 10.1021/acschembio.5b00897. Epub 2016 Jan 14.
4
Reduced GABAergic Action in the Autistic Brain.
Curr Biol. 2016 Jan 11;26(1):80-5. doi: 10.1016/j.cub.2015.11.019. Epub 2015 Dec 17.
5
Distinctive findings in a boy with Simpson-Golabi-Behmel syndrome.
Am J Med Genet A. 2016 Apr;170A(4):1035-9. doi: 10.1002/ajmg.a.37518. Epub 2015 Dec 22.
6
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
Neuron. 2015 Dec 2;88(5):910-917. doi: 10.1016/j.neuron.2015.11.009.
10
Characterizing autism spectrum disorders by key biochemical pathways.
Front Neurosci. 2015 Sep 24;9:313. doi: 10.3389/fnins.2015.00313. eCollection 2015.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验