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Species-Specific Changes in a Primate Transcription Factor Network Provide Insights into the Molecular Evolution of the Primate Prefrontal Cortex

机译:灵长类转录因子网络中特定物种的变化为灵长类前额叶皮层的分子进化提供了见识。

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摘要

The human prefrontal cortex (PFC) differs from that of other primates with respect to size, histology, and functional abilities. Here, we analyzed genome-wide expression data of humans, chimpanzees, and rhesus macaques to discover evolutionary changes in transcription factor (TF) networks that may underlie these phenotypic differences. We determined the co-expression networks of all TFs with species-specific expression including their potential target genes and interaction partners in the PFC of all three species. Integrating these networks allowed us inferring an ancestral network for all three species. This ancestral network as well as the networks for each species is enriched for genes involved in forebrain development, axonogenesis, and synaptic transmission. Our analysis allows us to directly compare the networks of each species to determine which links have been gained or lost during evolution. Interestingly, we detected that most links were gained on the human lineage, indicating increase TF cooperativity in humans. By comparing network changes between different tissues, we discovered that in brain tissues, but not in the other tissues, the human networks always had the highest connectivity. To pinpoint molecular changes underlying species-specific phenotypes, we analyzed the sub-networks of TFs derived only from genes with species-specific expression changes in the PFC. These sub-networks differed significantly in structure and function between the human and chimpanzee. For example, the human-specific sub-network is enriched for TFs implicated in cognitive disorders and for genes involved in synaptic plasticity and cognitive functions. Our results suggest evolutionary changes in TF networks that might have shaped morphological and functional differences between primate brains, in particular in the human PFC.
机译:人类前额叶皮层(PFC)在大小,组织学和功能能力方面与其他灵长类动物不同。在这里,我们分析了人类,黑猩猩和猕猴的全基因组表达数据,以发现可能构成这些表型差异的转录因子(TF)网络的进化变化。我们确定了所有具有物种特异性表达的TF的共表达网络,包括它们潜在的靶基因和这三种物种的PFC中的相互作用伙伴。整合这些网络可以让我们推断出这三个物种的祖先网络。这个祖先网络以及每个物种的网络都丰富了涉及前脑发育,轴突发生和突触传递的基因。我们的分析使我们可以直接比较每个物种的网络,以确定在进化过程中获得或失去了哪些联系。有趣的是,我们检测到大多数链接都是在人类谱系上获得的,这表明人类的TF合作性增强。通过比较不同组织之间的网络变化,我们发现在脑组织中,但在其他组织中却没有,人类网络始终具有最高的连通性。为了查明潜在的物种特定表型的分子变化,我们分析了仅由PFC中具有物种特定表达变化的基因衍生的TF的子网络。这些子网在人与黑猩猩之间的结构和功能上有很大不同。例如,人特异性子网丰富了与认知障碍有关的TF以及与突触可塑性和认知功能有关的基因。我们的结果表明,TF网络的进化变化可能已经塑造了灵长类大脑之间的形态和功能差异,特别是在人类PFC中。

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