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本文引用的文献

1
Dysregulation of protein synthesis and dendritic spine morphogenesis in ASD: studies in human pluripotent stem cells.自闭症谱系障碍中蛋白质合成和树突棘形态发生的失调:人类多能干细胞研究。
Mol Autism. 2020 May 27;11(1):40. doi: 10.1186/s13229-020-00349-y.
2
Elevated protein synthesis in microglia causes autism-like synaptic and behavioral aberrations.小胶质细胞中蛋白质合成的增加导致类似自闭症的突触和行为异常。
Nat Commun. 2020 Apr 14;11(1):1797. doi: 10.1038/s41467-020-15530-3.
3
Maternal Experience-Dependent Cortical Plasticity in Mice Is Circuit- and Stimulus-Specific and Requires MECP2.母鼠经验依赖性的小鼠大脑皮质可塑性具有回路和刺激特异性,需要 MeCP2。
J Neurosci. 2020 Feb 12;40(7):1514-1526. doi: 10.1523/JNEUROSCI.1964-19.2019. Epub 2020 Jan 7.
4
Atypical Response Properties of the Auditory Cortex of Awake MECP2-Overexpressing Mice.清醒状态下过表达MECP2的小鼠听觉皮层的非典型反应特性
Front Neurosci. 2019 May 7;13:439. doi: 10.3389/fnins.2019.00439. eCollection 2019.
5
Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.全基因组深度学习分析鉴定非编码突变对自闭症风险的贡献。
Nat Genet. 2019 Jun;51(6):973-980. doi: 10.1038/s41588-019-0420-0. Epub 2019 May 27.
6
Autism-linked dopamine transporter mutation alters striatal dopamine neurotransmission and dopamine-dependent behaviors.自闭症相关的多巴胺转运体突变改变纹状体多巴胺神经传递和多巴胺依赖的行为。
J Clin Invest. 2019 May 16;129(8):3407-3419. doi: 10.1172/JCI127411.
7
Mutation Interrupts Nucleolin-mTOR-P70S6K Signaling in Rett Syndrome Patients.突变中断雷特综合征患者的核仁素-mTOR-P70S6K信号通路。
Front Genet. 2018 Dec 19;9:635. doi: 10.3389/fgene.2018.00635. eCollection 2018.
8
ADNP Regulates Cognition: A Multitasking Protein.ADNP调节认知:一种多功能蛋白质。
Front Neurosci. 2018 Nov 26;12:873. doi: 10.3389/fnins.2018.00873. eCollection 2018.
9
Psychiatric comorbidities in autism spectrum disorder: A comparative study between DSM-IV-TR and DSM-5 diagnosis.自闭症谱系障碍中的精神共病:DSM-IV-TR与DSM-5诊断的比较研究
Int J Clin Health Psychol. 2016 Sep-Dec;16(3):266-275. doi: 10.1016/j.ijchp.2016.03.001. Epub 2016 Jun 3.
10
Regulatory discrimination of mRNAs by FMRP controls mouse adult neural stem cell differentiation.FMRP 通过对 mRNAs 的调控性识别来控制小鼠成体神经干细胞的分化。
Proc Natl Acad Sci U S A. 2018 Nov 27;115(48):E11397-E11405. doi: 10.1073/pnas.1809588115. Epub 2018 Oct 29.

自闭症谱系障碍中翻译和转录的相互控制。

Reciprocal control of translation and transcription in autism spectrum disorder.

机构信息

Center for Neural Science, New York University, New York, NY, USA.

出版信息

EMBO Rep. 2021 Jun 4;22(6):e52110. doi: 10.15252/embr.202052110. Epub 2021 May 11.

DOI:10.15252/embr.202052110
PMID:33977633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8183409/
Abstract

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.

摘要

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。