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人类在进化过程中,脑的大小和复杂程度得到了极大得增加。脑的结构使得人类有着区别于其他物种的极高的认知能力,比如语言能力,抽象思考能力等等。转录后修饰,如RNA编辑,可变剪切等能够由相同的DNA序列生成不同的RNA进而翻译成不同的蛋白质构体,是扩大蛋白质多样性的重要机制。随着二代测序发展,转录后修饰等已成为当今研究热点。
为了充分地评估转录后修饰在人脑在进化中的作用,张亚平院士课题组吴东东,叶凌群等对人脑的多个不同区域做了深度转录测序, 详细分析了可变剪切、RNA编辑、长链非编码RNA和年轻新基因的表达等。发现神经系统并未展示出较高程度的转录复杂度, 但是神经系统尤其是壳核(putamen)中存在非常高的RNA编辑活性,揭示了这个区域对于人的进化中的潜在的重要作用。同时发现了脑中的可变剪切和RNA编辑之间具有显著的关联,RNA编辑酶降低表达后,可变剪切事件也就增多,表明可变剪切和RNA编辑的分子机制之间可能存在竞争关系。另外基于此数据,进一步分析了人类新基因的表达模式,发现这些新基因不仅在新皮质中高表达,在其它脑组织中同样有一些富集,尤其是壳核(putamen)组织中富集大量新基因。
该项研究结果收录于Journal of Molecular Cell Biology在2015年出版的第4期专辑Collection: Innovative Methods and Techniques for Frontiers of Life Science,详情如下:
Abstract
Next-generation RNA sequencing has been successfully used for identification of transcript assembly, evaluation of gene expression levels, and detection of post-transcriptional modifications. Despite these large-scale studies, additional comprehensive RNA-seq data from different subregions of the human brain are required to fully evaluate the evolutionary patterns experienced by the human brain transcriptome. Here, we provide a total of 6.5 billion RNA-seq reads from different subregions of the human brain. A significant correlation was observed between the levels of alternative splicing and RNA editing, which might be explained by a competition between the molecular machineries responsible for the splicing and editing of RNA. Young human protein-coding genes demonstrate biased expression to the neocortical and non-neocortical regions during evolution on the lineage leading to humans. We also found that a significantly greater number of young human protein-coding genes are expressed in the putamen, a tissue that was also observed to have the highest level of RNA-editing activity. The putamen, which previously received little attention, plays an important role in cognitive ability, and our data suggest a potential contribution of the putamen to human evolution.
J Mol Cell Biol (2015)7 (4):314-325 first published online July 17, 2015 doi:10.1093/jmcb/mjv043
Keywords: RNA editing, human brain transcriptome, young gene, human brain evolution
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