Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Elife. 2018 Mar 21;7:e32332. doi: 10.7554/eLife.32332.
Understanding the molecular basis that underlies the expansion of the neocortex during primate, and notably human, evolution requires the identification of genes that are particularly active in the neural stem and progenitor cells of the developing neocortex. Here, we have used existing transcriptome datasets to carry out a comprehensive screen for protein-coding genes preferentially expressed in progenitors of fetal human neocortex. We show that 15 human-specific genes exhibit such expression, and many of them evolved distinct neural progenitor cell-type expression profiles and levels compared to their ancestral paralogs. Functional studies on one such gene, , demonstrate its ability to promote basal progenitor proliferation in mice. An additional 35 human genes with progenitor-enriched expression are shown to have orthologs only in primates. Our study provides a resource of genes that are promising candidates to exert specific, and novel, roles in neocortical development during primate, and notably human, evolution.
理解灵长类动物(尤其是人类)进化过程中大脑新皮质扩张的分子基础,需要鉴定在神经干细胞和祖细胞中特别活跃的基因。在这里,我们利用现有的转录组数据集,对胎儿人类大脑新皮质祖细胞中优先表达的蛋白质编码基因进行了全面筛选。我们发现 15 个人类特有的基因具有这种表达特性,其中许多基因与它们的祖先基因相比,在神经祖细胞类型的表达谱和水平上表现出明显的差异。对其中一个基因 (SLC1A3)的功能研究表明,它能够促进小鼠基底祖细胞的增殖。另外 35 个具有祖细胞富集表达的人类基因仅在灵长类动物中具有同源基因。我们的研究提供了一个有希望的候选基因资源,这些基因可能在灵长类动物(尤其是人类)进化过程中大脑新皮质的发育中发挥特定的、新颖的作用。