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Genes encoding SATB2-interacting proteins in adult cerebral cortex contribute to human cognitive ability

机译:成人大脑皮层中编码SATB2相互作用蛋白的基因有助于人类认知能力

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摘要

During CNS development, the nuclear protein SATB2 is expressed in superficial cortical layers and determines projection neuron identity. In the adult CNS, SATB2 is expressed in pyramidal neurons of all cortical layers and is a regulator of synaptic plasticity and long-term memory. Common variation in SATB2 locus confers risk of schizophrenia, whereas rare, de novo structural and single nucleotide variants cause severe intellectual disability and absent or limited speech. To characterize differences in SATB2 molecular function in developing vs adult neocortex, we isolated SATB2 protein interactomes at the two ontogenetic stages and identified multiple novel SATB2 interactors. SATB2 interactomes are highly enriched for proteins that stabilize de novo chromatin loops. The comparison between the neonatal and adult SATB2 protein complexes indicates a developmental shift in SATB2 molecular function, from transcriptional repression towards organization of chromosomal superstructure. Accordingly, gene sets regulated by SATB2 in the neocortex of neonatal and adult mice show limited overlap. Genes encoding SATB2 protein interactors were grouped for gene set analysis of human GWAS data. Common variants associated with human cognitive ability are enriched within the genes encoding adult but not neonatal SATB2 interactors. Our data support a shift in the function of SATB2 in cortex over lifetime and indicate that regulation of spatial chromatin architecture by the SATB2 interactome contributes to cognitive function in the general population.
机译:在中枢神经系统发育过程中,核蛋白SATB2在浅层皮层中表达并确定投射神经元的身份。在成人中枢神经系统中,SATB2在所有皮质层的锥体神经元中表达,并且是突触可塑性和长期记忆的调节剂。 SATB2基因座的常见变异会带来精神分裂症的风险,而罕见的,从头开始的结构变异和单核苷酸变异会导致严重的智力障碍和缺乏或有限的言语。为了表征发育中的和成人新皮质中SATB2分子功能的差异,我们在两个个体发育阶段分离了SATB2蛋白相互作用组,并鉴定了多个新型SATB2相互作用因子。 SATB2相互作用基因组富含稳定从头染色质环的蛋白质。新生儿和成人SATB2蛋白复合物之间的比较表明,SATB2分子功能从转录抑制向染色体上层结构的组织发展转变。因此,新生鼠和成年鼠的新皮层中由SATB2调控的基因集显示出有限的重叠。编码SATB2蛋白相互作用子的基因被分组用于人类GWAS数据的基因组分析。与人类认知能力相关的常见变体富含编码成人而不是新生儿SATB2相互作用子的基因。我们的数据支持SATB2在整个皮质中的功能随着寿命的推移而发生变化,并表明SATB2相互作用组对空间染色质结构的调节有助于普通人群的认知功能。

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