首页> 美国卫生研究院文献>Frontiers in Neuroanatomy >Parallel Development of Chromatin Patterns Neuron Morphology and Connections: Potential for Disruption in Autism
【2h】

Parallel Development of Chromatin Patterns Neuron Morphology and Connections: Potential for Disruption in Autism

机译:染色质模式神经元形态和联系的平行发展:自闭症的破坏潜力

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The phenotype of neurons and their connections depend on complex genetic and epigenetic processes that regulate the expression of genes in the nucleus during development and throughout life. Here we examined the distribution of nuclear chromatin patters in relation to the epigenetic landscape, phenotype and connections of neurons with a focus on the primate cerebral cortex. We show that nuclear patterns of chromatin in cortical neurons are related to neuron size and cortical connections. Moreover, we point to evidence that reveals an orderly sequence of events during development, linking chromatin and gene expression patterns, neuron morphology, function, and connections across cortical areas and layers. Based on this synthesis, we posit that systematic studies of changes in chromatin patterns and epigenetic marks across cortical areas will provide novel insights on the development and evolution of cortical networks, and their disruption in connectivity disorders of developmental origin, like autism. Achieving this requires embedding and interpreting genetic, transcriptional, and epigenetic studies within a framework that takes into consideration distinct types of neurons, local circuit interactions, and interareal pathways. These features vary systematically across cortical areas in parallel with laminar structure and are differentially affected in disorders. Finally, based on evidence that autism-associated genetic polymorphisms are especially prominent in excitatory neurons and connectivity disruption affects mostly limbic cortices, we employ this systematic approach to propose novel, targeted studies of projection neurons in limbic areas to elucidate the emergence and time-course of developmental disruptions in autism.
机译:神经元的表型及其联系取决于复杂的遗传和表观遗传过程,这些过程在发育和整个生命过程中调节细胞核中基因的表达。在这里,我们研究了与灵长类动物大脑皮层相关的表观遗传景观,表型和神经元联系的核染色质模式分布。我们表明,皮质神经元中染色质的核型与神经元大小和皮质连接有关。此外,我们指出的证据揭示了发育过程中的有序事件,将染色质和基因表达模式,神经元形态,功能以及跨皮质区域和层的连接联系在一起。基于这种综合,我们认为,对整个皮质区域的染色质模式和表观遗传标记的变化进行系统的研究,将为皮质网络的发展和进化及其对诸如自闭症等发展起源的连通性障碍的破坏提供新颖的见解。要实现这一点,需要在考虑了神经元的不同类型,局部回路相互作用和区域间通路的框架内嵌入和解释遗传,转录和表观遗传学研究。这些特征在与层状结构平行的整个皮质区域内系统地变化,并且在疾病中受到不同的影响。最后,基于证据表明自闭症相关的遗传多态性在兴奋性神经元中尤为突出,而连接破坏主要影响边缘皮质,我们采用这种系统性方法提出了针对性的,针对性的研究,旨在研究边缘区域中投射神经元的出现和时程自闭症的发展障碍。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号