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本文引用的文献

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Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex.发育皮层中 FMRP 对 NOS1 的种属依赖性转录后调控。
Cell. 2012 May 11;149(4):899-911. doi: 10.1016/j.cell.2012.02.060.
2
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.SOX5 基因在 12p12.1 上的杂合性缺失与发育迟缓有关,其主要表现为语言发育迟缓、行为问题和轻度的发育异常特征。
Hum Mutat. 2012 Apr;33(4):728-40. doi: 10.1002/humu.22037.
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COUP-TFI promotes radial migration and proper morphology of callosal projection neurons by repressing Rnd2 expression.COUP-TFI 通过抑制 Rnd2 表达促进胼胝体投射神经元的放射状迁移和正确形态发生。
Development. 2011 Nov;138(21):4685-97. doi: 10.1242/dev.068031. Epub 2011 Sep 28.
4
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.CNTNAP2 的缺失导致癫痫、神经元迁移异常和核心自闭症相关缺陷。
Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040.
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Satb2 is required for dendritic arborization and soma spacing in mouse cerebral cortex.Satb2 对于小鼠大脑皮层的树突分支和胞体间距是必需的。
Cereb Cortex. 2012 Jul;22(7):1510-9. doi: 10.1093/cercor/bhr215. Epub 2011 Sep 1.
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A copy number variation morbidity map of developmental delay.发育迟缓的拷贝数变异发病率图。
Nat Genet. 2011 Aug 14;43(9):838-46. doi: 10.1038/ng.909.
7
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.多种反复出现的新生拷贝数变异,包括 7q11.23 威廉姆斯综合征区域的重复,与自闭症强烈相关。
Neuron. 2011 Jun 9;70(5):863-85. doi: 10.1016/j.neuron.2011.05.002.
8
Proneural transcription factors regulate different steps of cortical neuron migration through Rnd-mediated inhibition of RhoA signaling.神经前转录因子通过 Rnd 介导的 RhoA 信号抑制调节皮质神经元迁移的不同步骤。
Neuron. 2011 Mar 24;69(6):1069-84. doi: 10.1016/j.neuron.2011.02.018.
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Excitatory projection neuron subtypes control the distribution of local inhibitory interneurons in the cerebral cortex.兴奋性投射神经元亚型控制大脑皮层局部抑制性中间神经元的分布。
Neuron. 2011 Feb 24;69(4):763-79. doi: 10.1016/j.neuron.2011.01.015.
10
Dorsal radial glial cells have the potential to generate cortical interneurons in human but not in mouse brain.背侧桡侧神经胶质细胞有可能在人类大脑中产生皮质中间神经元,但在小鼠大脑中则不行。
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转录调控新皮层神经元迁移和层状特征

Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex.

机构信息

Department of Neurobiology and Kavli Institute for Neuroscience, Yale University School of Medicine, New Haven, CT 06510, USA.

出版信息

Development. 2012 May;139(9):1535-46. doi: 10.1242/dev.069963.

DOI:10.1242/dev.069963
PMID:22492350
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3317962/
Abstract

The cerebral neocortex is segregated into six horizontal layers, each containing unique populations of molecularly and functionally distinct excitatory projection (pyramidal) neurons and inhibitory interneurons. Development of the neocortex requires the orchestrated execution of a series of crucial processes, including the migration of young neurons into appropriate positions within the nascent neocortex, and the acquisition of layer-specific neuronal identities and axonal projections. Here, we discuss emerging evidence supporting the notion that the migration and final laminar positioning of cortical neurons are also co-regulated by cell type- and layer-specific transcription factors that play concomitant roles in determining the molecular identity and axonal connectivity of these neurons. These transcriptional programs thus provide direct links between the mechanisms controlling the laminar position and identity of cortical neurons.

摘要

大脑新皮层分为 6 个水平层,每个层都包含独特的分子和功能上不同的兴奋性投射(锥体细胞)神经元和抑制性中间神经元群体。新皮层的发育需要协调执行一系列关键过程,包括年轻神经元迁移到初生新皮层中的适当位置,以及获得层特异性神经元身份和轴突投射。在这里,我们讨论了支持以下观点的新证据,即皮质神经元的迁移和最终层状定位也受到细胞类型特异性和层特异性转录因子的共同调节,这些转录因子在确定这些神经元的分子身份和轴突连接方面发挥着伴随作用。这些转录程序因此在控制皮质神经元的层状位置和身份的机制之间提供了直接联系。