Cavallaro Sebastiano
Functional Genomics Center, Institute of Neurological Sciences, Italian National Research Council (CNR), Via Paolo Gaifami 18, Catania, 95126, Italy,
Methods Mol Biol. 2015;1254:141-51. doi: 10.1007/978-1-4939-2152-2_11.
Neuronal apoptosis represents an intrinsic «suicide» program, by which a neuron orchestrates its own destruction. Although engagement of apoptosis requires transcription and protein synthesis, the complete spectrum of genes involved in distinct temporal domains remained unknown until the advent of genomics. In the last 10 years, the genome sequences and the development of high-throughput genomic technologies, such as DNA microarrays, have offered the unprecedented experimental opportunities to explore the transcriptional mechanisms underlying apoptosis from a new systems-level perspective. This review goes over this genomic approach and illustrates the use of microarray methodology to dissecting the multigenic program underlying neuronal apoptosis.
神经元凋亡代表一种内在的“自杀”程序,通过该程序神经元精心安排自身的破坏。尽管凋亡的启动需要转录和蛋白质合成,但在基因组学出现之前,参与不同时间域的完整基因谱仍不为人知。在过去十年中,基因组序列以及诸如DNA微阵列等高通量基因组技术的发展,为从新的系统水平视角探索凋亡背后的转录机制提供了前所未有的实验机会。本综述回顾了这种基因组学方法,并阐述了使用微阵列方法剖析神经元凋亡背后的多基因程序。