Peters M A, Taparowsky E J
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907-1392, USA.
Crit Rev Eukaryot Gene Expr. 1998;8(3-4):277-96. doi: 10.1615/critreveukargeneexpr.v8.i3-4.30.
Precisely how the Myc proteins promote cellular growth and transformation remains an enigma. Structural and functional studies unequivocally demonstrate that Myc proteins have the potential to function as regulators of gene transcription in vivo. Therefore, the current view is that Myc-induced cellular growth is orchestrated by products of the genes regulated by Myc and that efforts to curtail Myc function are best directed toward the accessory proteins that interact with Myc to modulate its function as a transcription factor. This review is focused on recent work designed to identify the genetic targets of Myc activity in cells and to characterize Myc-interacting proteins. These studies have provided an intriguing set of molecular tools that can be exploited to generate new information on the role of Myc in cell growth and oncogenic transformation.
Myc蛋白究竟如何促进细胞生长和转化仍是一个谜。结构和功能研究明确表明,Myc蛋白在体内有作为基因转录调节因子发挥作用的潜力。因此,当前的观点是,Myc诱导的细胞生长是由Myc调控的基因产物精心安排的,并且抑制Myc功能的努力最好针对与Myc相互作用以调节其作为转录因子功能的辅助蛋白。本综述聚焦于旨在鉴定细胞中Myc活性的遗传靶点并表征与Myc相互作用蛋白的近期研究工作。这些研究提供了一组有趣的分子工具,可用于生成关于Myc在细胞生长和致癌转化中作用的新信息。