Center for Neural Science, New York University, New York, NY, USA.
EMBO Rep. 2021 Jun 4;22(6):e52110. doi: 10.15252/embr.202052110. Epub 2021 May 11.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication and the presence of restricted patterns of interest and repetitive behaviors. ASD is genetically heterogeneous and is believed to be caused by both inheritable and de novo gene variations. Studies have revealed an extremely complex genetic landscape of ASD, favoring the idea that mutations in different clusters of genes interfere with interconnected downstream signaling pathways and circuitry, resulting in aberrant behavior. In this review, we describe a select group of candidate genes that represent both syndromic and non-syndromic forms of ASD and encode proteins that are important in transcriptional and translational regulation. We focus on the interplay between dysregulated translation and transcription in ASD with the hypothesis that dysregulation of each synthetic process triggers a feedback loop to act on the other, which ultimately exacerbates ASD pathophysiology. Finally, we summarize findings from interdisciplinary studies that pave the way for the investigation of the cooperative impact of different genes and pathways underlying the development of ASD.
自闭症谱系障碍(ASD)是一种神经发育障碍,其特征是社交沟通缺陷,以及存在受限的兴趣模式和重复行为。ASD 具有遗传异质性,据信是由可遗传和从头基因变异引起的。研究揭示了 ASD 极其复杂的遗传景观,支持这样一种观点,即不同基因簇的突变会干扰相互连接的下游信号通路和电路,导致异常行为。在这篇综述中,我们描述了一组选定的候选基因,它们代表了 ASD 的综合征和非综合征形式,并编码在转录和翻译调节中重要的蛋白质。我们专注于 ASD 中失调的翻译和转录之间的相互作用,假设每个合成过程的失调都会触发一个反馈回路作用于另一个过程,最终加剧 ASD 的病理生理学。最后,我们总结了跨学科研究的发现,为研究 ASD 发展背后不同基因和途径的协同影响铺平了道路。