Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Am J Hum Biol. 2013 May-Jun;25(3):418-30. doi: 10.1002/ajhb.22394. Epub 2013 Apr 4.
Human brain development follows a unique pattern characterized by a prolonged period of postnatal growth and reorganization, and a postnatal peak in glucose utilization. The molecular processes underlying these developmental changes are poorly characterized. The objectives of this study were to determine developmental trajectories of gene expression and to examine the evolutionary history of genes differentially expressed as a function of age.
We used microarrays to determine age-related patterns of mRNA expression in human cerebral cortical samples ranging from infancy to adulthood. In contrast to previous developmental gene expression studies of human neocortex that relied on postmortem tissue, we measured mRNA expression from the nondiseased margins of surgically resected tissue. We used regression models designed to identify transcripts that followed significant linear or curvilinear functions of age and used population genetics techniques to examine the evolution of these genes.
We identified 40 transcripts with significant age-related trajectories in expression. Ten genes have documented roles in nervous system development and energy metabolism, others are novel candidates in brain development. Sixteen transcripts showed similar patterns of expression, characterized by decreasing expression during childhood. Comparative genomic analyses revealed that the regulatory regions of three genes have evidence of adaptive evolution in recent human evolution.
These findings provide evidence that a subset of genes expressed in the human cerebral cortex broadly mirror developmental patterns of cortical glucose consumption. Whether there is a causal relationship between gene expression and glucose utilization remains to be determined.
人类大脑的发育遵循一种独特的模式,其特点是出生后的生长和重组期较长,以及出生后葡萄糖利用率达到峰值。这些发育变化背后的分子过程还没有得到很好的描述。本研究的目的是确定基因表达的发育轨迹,并研究随年龄变化而差异表达的基因的进化历史。
我们使用微阵列来确定从婴儿期到成年期的人类大脑皮质样本中与年龄相关的 mRNA 表达模式。与之前依赖于死后组织的人类新皮质发育基因表达研究不同,我们从手术切除的无病变组织边缘测量了 mRNA 表达。我们使用回归模型来识别遵循年龄显著线性或曲线函数的转录本,并使用群体遗传学技术来研究这些基因的进化。
我们确定了 40 个具有显著年龄相关表达轨迹的转录本。10 个基因在神经系统发育和能量代谢方面具有明确的作用,其他基因是大脑发育的新候选基因。16 个转录本表现出相似的表达模式,特征是在儿童期表达下降。比较基因组分析显示,三个基因的调控区域有最近人类进化中适应性进化的证据。
这些发现提供了证据表明,在人类大脑皮质中表达的一组基因广泛反映了皮质葡萄糖消耗的发育模式。基因表达和葡萄糖利用之间是否存在因果关系仍有待确定。