Fritzsch Bernd, Jahan Israt, Pan Ning, Elliott Karen L
Department of Biology, University of Iowa, CLAS, 143 BB, Iowa City, IA, 52242, USA,
Cell Tissue Res. 2015 Jan;359(1):295-313. doi: 10.1007/s00441-014-2043-1. Epub 2014 Nov 23.
Understanding the evolution of the neurosensory system of man, able to reflect on its own origin, is one of the major goals of comparative neurobiology. Details of the origin of neurosensory cells, their aggregation into central nervous systems and associated sensory organs and their localized patterning leading to remarkably different cell types aggregated into variably sized parts of the central nervous system have begun to emerge. Insights at the cellular and molecular level have begun to shed some light on the evolution of neurosensory cells, partially covered in this review. Molecular evidence suggests that high mobility group (HMG) proteins of pre-metazoans evolved into the definitive Sox [SRY (sex determining region Y)-box] genes used for neurosensory precursor specification in metazoans. Likewise, pre-metazoan basic helix-loop-helix (bHLH) genes evolved in metazoans into the group A bHLH genes dedicated to neurosensory differentiation in bilaterians. Available evidence suggests that the Sox and bHLH genes evolved a cross-regulatory network able to synchronize expansion of precursor populations and their subsequent differentiation into novel parts of the brain or sensory organs. Molecular evidence suggests metazoans evolved patterning gene networks early, which were not dedicated to neuronal development. Only later in evolution were these patterning gene networks tied into the increasing complexity of diffusible factors, many of which were already present in pre-metazoans, to drive local patterning events. It appears that the evolving molecular basis of neurosensory cell development may have led, in interaction with differentially expressed patterning genes, to local network modifications guiding unique specializations of neurosensory cells into sensory organs and various areas of the central nervous system.
理解人类神经感觉系统的进化,即能够反思其自身起源,是比较神经生物学的主要目标之一。神经感觉细胞的起源细节、它们聚集形成中枢神经系统和相关感觉器官的过程,以及它们的局部模式形成,导致显著不同的细胞类型聚集在中枢神经系统大小各异的部分,这些细节已开始显现。细胞和分子层面的见解已开始为神经感觉细胞的进化提供一些线索,本综述将部分涵盖这些内容。分子证据表明,后生动物之前的高迁移率族(HMG)蛋白进化为后生动物中用于神经感觉前体特化的决定性Sox [SRY(性别决定区Y)-盒]基因。同样,后生动物之前的基本螺旋-环-螺旋(bHLH)基因在后生动物中进化为双侧对称动物中专门用于神经感觉分化的A组bHLH基因。现有证据表明,Sox和bHLH基因进化出了一个交叉调节网络,能够同步前体细胞群的扩张及其随后分化为大脑或感觉器官的新部分。分子证据表明,后生动物早期就进化出了模式形成基因网络,但这些网络并非专门用于神经元发育。只是在进化后期,这些模式形成基因网络才与越来越复杂的可扩散因子联系起来,其中许多因子在后生动物之前就已存在,以驱动局部模式形成事件。看来,神经感觉细胞发育不断演变的分子基础可能与差异表达的模式形成基因相互作用,导致局部网络发生改变,从而引导神经感觉细胞独特地特化为感觉器官和中枢神经系统的各个区域。