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Mean Expression of the X-Chromosome is Associated with Neuronal Density

机译:X染色体的平均表达与神经元密度有关。

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Neurodegenerative diseases are characterised by neuronal loss. Neuronal loss causes a varying density of neurons across samples which confounds results from gene expression studies. Chromosome X is known to be specifically important in brain. We hypothesised the existence of a chromosomal signature of gene expression associated with the X-chromosome for neurological conditions not normally associated with that chromosome. The hypothesis was investigated using microarray datasets from studies on Parkinson's disease, Alzheimer's disease and Huntington's disease. Data were analysed using Chromowave, an analytical tool for detecting spatially extended expression changes across chromosomes. To examine associations with neuronal density, expressions from a set of neuron specific genes were extracted. The association between these genes and the expression patterns extracted by Chromowave was then analyzed. We observed an extended pattern of low expression of ChrX consistent in all the neurodegenerative disease brain datasets. There was a strong correlation between mean ChrX expression and the pattern extracted from the autosomal neuronal specific genes, but no correlation with mean autosomal expression. No chromosomal patterns associated with the neuron specific genes were found on other chromosomes. The chromosomal expression pattern was not present in datasets from blood cells. The ChrX:Autosome expression ratio was also higher in neuronal cells than in tissues with a mix of cell types. The results suggest that a loss of neurons manifests in gene expression experiments primarily as a reduction in mean expression of genes along ChrX. The most likely explanation for this finding relates to the documented general up-regulation of ChrX in brain tissue which, this work suggests, occurs primarily in neurons. The purpose and mechanisms behind this cell specific higher expression warrant further research, which may also help elucidate connectio.
机译:神经变性疾病的特征是神经元丢失。神经元丢失导致样本中神经元密度的变化,这混淆了基因表达研究的结果。已知X染色体在大脑中特别重要。我们假设存在与X染色体相关的基因表达的染色体特征,而这些特征通常与该染色体无关。使用关于帕金森氏病,阿尔茨海默氏病和亨廷顿氏病的研究的微阵列数据集研究了该假设。使用Chromowave(一种用于检测跨染色体空间扩展表达变化的分析工具)分析数据。为了检查与神经元密度的关联,提取了一组神经元特异性基因的表达。然后分析了这些基因与通过Chromowave提取的表达模式之间的关联。我们观察到在所有神经退行性疾病脑数据集中一致的ChrX低表达的扩展模式。平均ChrX表达与从常染色体神经元特异性基因提取的模式之间有很强的相关性,但与平均常染色体表达无相关性。在其他染色体上未发现与神经元特定基因相关的染色体模式。血细胞数据集中没有染色体表达模式。在神经元细胞中,ChrX:常染色体的表达率也高于具有多种细胞类型的组织。结果表明,神经元的丧失主要在基因表达实验中表现为沿ChrX的基因平均表达减少。这项发现最可能的解释是有记载的脑组织中ChrX的总体上调,这项工作表明,它主要发生在神经元中。这种细胞特异性更高表达背后的目的和机制值得进一步研究,这也可能有助于阐明连接。

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