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在人类诱导神经元中进行的蛋白质相互作用研究表明,自闭症谱系障碍存在共同的生物学基础。

Protein interaction studies in human induced neurons indicate convergent biology underlying autism spectrum disorders.

作者信息

Pintacuda Greta, Hsu Yu-Han H, Tsafou Kalliopi, Li Ka Wan, Martín Jacqueline M, Riseman Jackson, Biagini Julia C, Ching Joshua K T, Mena Daya, Gonzalez-Lozano Miguel A, Egri Shawn B, Jaffe Jake, Smit August B, Fornelos Nadine, Eggan Kevin C, Lage Kasper

机构信息

Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Novo Nordisk Foundation Center for Genomic Mechanisms of Disease, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

出版信息

Cell Genom. 2023 Jan 24;3(3):100250. doi: 10.1016/j.xgen.2022.100250. eCollection 2023 Mar 8.

Abstract

Autism spectrum disorders (ASDs) have been linked to genes with enriched expression in the brain, but it is unclear how these genes converge into cell-type-specific networks. We built a protein-protein interaction network for 13 ASD-associated genes in human excitatory neurons derived from induced pluripotent stem cells (iPSCs). The network contains newly reported interactions and is enriched for genetic and transcriptional perturbations observed in individuals with ASDs. We leveraged the network data to show that the ASD-linked brain-specific isoform of ANK2 is important for its interactions with synaptic proteins and to characterize a PTEN-AKAP8L interaction that influences neuronal growth. The IGF2BP1-3 complex emerged as a convergent point in the network that may regulate a transcriptional circuit of ASD-associated genes. Our findings showcase cell-type-specific interactomes as a framework to complement genetic and transcriptomic data and illustrate how both individual and convergent interactions can lead to biological insights into ASDs.

摘要

自闭症谱系障碍(ASD)与在大脑中表达丰富的基因有关,但尚不清楚这些基因如何汇聚成细胞类型特异性网络。我们构建了一个蛋白质-蛋白质相互作用网络,该网络涉及来自诱导多能干细胞(iPSC)的人类兴奋性神经元中的13个与ASD相关的基因。该网络包含新报道的相互作用,并且富含在ASD个体中观察到的遗传和转录扰动。我们利用网络数据表明,ANK2的ASD相关脑特异性异构体对其与突触蛋白的相互作用很重要,并表征了影响神经元生长的PTEN-AKAP8L相互作用。IGF2BP1-3复合物成为网络中的一个汇聚点,可能调节ASD相关基因的转录回路。我们的研究结果展示了细胞类型特异性相互作用组作为补充遗传和转录组数据的框架,并说明了个体和汇聚相互作用如何能够带来对ASD的生物学见解。

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