Hartl Markus, Bister Klaus
Center for Chemistry and Biomedicine, Institute of Biochemistry, University of Innsbruck, Innsbruck, Austria.
Methods Mol Biol. 2013;1012:21-49. doi: 10.1007/978-1-62703-429-6_3.
The myc oncogene was originally identified as a transduced allele (v-myc) in the genome of a highly oncogenic avian retrovirus. The protein product (Myc) of the cellular c-myc proto-oncogene represents the key component of a transcription factor network controlling the expression of a large fraction of all human genes. Myc regulates fundamental cellular processes like growth, metabolism, proliferation, differentiation, and apoptosis. Mutational deregulation of c-myc leading to increased levels of the Myc protein is a frequent event in the etiology of human cancers. In this chapter, we describe cell systems and experimental strategies to monitor and quantify the oncogenic potential of myc alleles and to isolate and characterize transcriptional targets of Myc that are relevant for the cell transformation process. We also describe experimental procedures to study the evolutionary origin of myc and to analyze structure and function of the ancestral myc proto-oncogenes.
myc癌基因最初是在一种高度致癌的禽逆转录病毒基因组中作为转导等位基因(v-myc)被鉴定出来的。细胞c-myc原癌基因的蛋白质产物(Myc)是一个转录因子网络的关键组成部分,该网络控制着所有人类基因中很大一部分的表达。Myc调节诸如生长、代谢、增殖、分化和凋亡等基本细胞过程。导致Myc蛋白水平升高的c-myc突变失调是人类癌症病因中常见的事件。在本章中,我们描述了细胞系统和实验策略,以监测和量化myc等位基因的致癌潜力,并分离和鉴定与细胞转化过程相关的Myc转录靶点。我们还描述了研究myc进化起源以及分析祖先c-myc原癌基因结构和功能的实验程序。