Hume David A, Wells Christine A, Ravasi Timothy
ARC Special Research Centre for Functional and Applied Genomics and CRC for Chronic Inflammatory Diseases, Institute for Molecular Bioscience, University of Queensland, Australia.
Novartis Found Symp. 2007;281:2-18; discussion 18-24, 50-3, 208-9. doi: 10.1002/9780470062128.ch2.
The functions of macrophages in the innate immune system require the constitutive expression of a wide range of myeloid-specific genes, including various pattern recognition receptors, as well as the inducible expression of a suite of genes required to initiate inflammation and eliminate pathogens. Our overall aim is to understand the transcriptional networks that underlie both macrophage-specific transcription and the response to pathogen components such as lipopolysaccharide (LPS). The approaches used include detailed functional analysis of specific promoters, such as that of the CSF1 receptor, global cDNA microarray expression profiling, high throughput real-time PCR analysis of all the transcription factors encoded by the mammalian genome, full length cDNA library construction and sequencing, CAGE analysis to identify specific promoters used in macrophages and motif analysis to detect candidate cis-acting elements in co-regulated genes in macrophages. This review discusses some of the progress in moving towards a transcriptional network model for mouse macrophage activation by LPS, as well as insight into the role of alternative promoter usage and polyadenylation in generating functional protein variants that impact on signalling in macrophages.
巨噬细胞在先天性免疫系统中的功能需要多种髓系特异性基因的组成性表达,包括各种模式识别受体,以及启动炎症和清除病原体所需的一组基因的诱导性表达。我们的总体目标是了解构成巨噬细胞特异性转录以及对病原体成分(如脂多糖,LPS)反应基础的转录网络。所采用的方法包括对特定启动子(如CSF1受体的启动子)进行详细的功能分析、全基因组cDNA微阵列表达谱分析、对哺乳动物基因组编码的所有转录因子进行高通量实时PCR分析、全长cDNA文库构建与测序、CAGE分析以鉴定巨噬细胞中使用的特定启动子,以及基序分析以检测巨噬细胞中共同调控基因中的候选顺式作用元件。本综述讨论了在建立LPS激活小鼠巨噬细胞的转录网络模型方面取得的一些进展,以及对可变启动子使用和聚腺苷酸化在产生影响巨噬细胞信号传导的功能性蛋白质变体中的作用的见解。