Harkin Lauren F, Lindsay Susan J, Xu Yaobo, Alzu'bi Ayman, Ferrara Alexandra, Gullon Emily A, James Owen G, Clowry Gavin J
Institute of Neuroscience, Newcastle University, Framlington Place, Newcastle upon Tyne NE2 4HH, UK.
Institute of Genetic Medicine, Newcastle University, International Centre for Life, Parkway Drive, Newcastle upon Tyne NE1 3BZ, UK.
Cereb Cortex. 2017 Jan 1;27(1):216-232. doi: 10.1093/cercor/bhw394.
Neurexins (NRXNs) are presynaptic terminal proteins and candidate neurodevelopmental disorder susceptibility genes; mutations presumably upset synaptic stabilization and function. However, analysis of human cortical tissue samples by RNAseq and quantitative real-time PCR at 8-12 postconceptional weeks, prior to extensive synapse formation, showed expression of all three NRXNs as well as several potential binding partners. However, the levels of expression were not identical; NRXN1 increased with age and NRXN2 levels were consistently higher than for NRXN3. Immunohistochemistry for each NRXN also revealed different expression patterns at this stage of development. NRXN1 and NRXN3 immunoreactivity was generally strongest in the cortical plate and increased in the ventricular zone with age, but was weak in the synaptogenic presubplate (pSP) and marginal zone. On the other hand, NRXN2 colocalized with synaptophysin in neurites of the pSP, but especially with GAP43 and CASK in growing axons of the intermediate zone. Alternative splicing modifies the role of NRXNs and we found evidence by RNAseq for exon skipping at splice site 4 and concomitant expression of KHDBRS proteins which control this splicing. NRXN2 may play a part in early cortical synaptogenesis, but NRXNs could have diverse roles in development including axon guidance, and intercellular communication between proliferating cells and/or migrating neurons.
神经连接蛋白(NRXNs)是突触前末端蛋白和候选神经发育障碍易感基因;突变可能会破坏突触的稳定和功能。然而,在受孕后8-12周广泛突触形成之前,通过RNA测序和定量实时PCR对人类皮质组织样本进行分析,结果显示所有三种NRXNs以及几种潜在的结合伴侣均有表达。然而,表达水平并不相同;NRXN1随年龄增长而增加,NRXN2的水平始终高于NRXN3。对每种NRXN进行免疫组织化学分析也揭示了在这个发育阶段不同的表达模式。NRXN1和NRXN3的免疫反应性通常在皮质板中最强,并随年龄在脑室区增加,但在突触发生前板(pSP)和边缘区较弱。另一方面,NRXN2在pSP的神经突中与突触素共定位,但在中间区生长的轴突中尤其与GAP43和CASK共定位。可变剪接改变了NRXNs的作用,我们通过RNA测序发现了剪接位点4外显子跳跃以及控制这种剪接的KHDBRS蛋白伴随表达的证据。NRXN2可能在早期皮质突触形成中起作用,但NRXNs在发育中可能具有多种作用,包括轴突导向以及增殖细胞和/或迁移神经元之间的细胞间通讯。