Ogbourne S, Antalis T M
Queensland Cancer Fund Experimental Oncology Program, The Queensland Institute of Medical Research, Brisbane, 4029 Queensland, Australia.
Biochem J. 1998 Apr 1;331 ( Pt 1)(Pt 1):1-14. doi: 10.1042/bj3310001.
Mechanisms controlling transcription and its regulation are fundamental to our understanding of molecular biology and, ultimately, cellular biology. Our knowledge of transcription initiation and integral factors such as RNA polymerase is considerable, and more recently our understanding of the involvement of enhancers and complexes such as holoenzyme and mediator has increased dramatically. However, an understanding of transcriptional repression is also essential for a complete understanding of promoter structure and the regulation of gene expression. Transcriptional repression in eukaryotes is achieved through 'silencers', of which there are two types, namely 'silencer elements' and 'negative regulatory elements' (NREs). Silencer elements are classical, position-independent elements that direct an active repression mechanism, and NREs are position-dependent elements that direct a passive repression mechanism. In addition, 'repressors' are DNA-binding trasncription factors that interact directly with silencers. A review of the recent literature reveals that it is the silencer itself and its context within a given promoter, rather than the interacting repressor, that determines the mechanism of repression. Silencers form an intrinsic part of many eukaryotic promoters and, consequently, knowledge of their interactive role with enchancers and other transcriptional elements is essential for our understanding of gene regulation in eukaryotes.
控制转录及其调控的机制是我们理解分子生物学乃至细胞生物学的基础。我们对转录起始以及诸如RNA聚合酶等整合因子已有相当多的了解,最近我们对增强子以及诸如全酶和中介体等复合物参与情况的理解也有了显著增加。然而,对于转录抑制的理解对于全面理解启动子结构和基因表达调控同样至关重要。真核生物中的转录抑制是通过“沉默子”实现的,沉默子有两种类型,即“沉默子元件”和“负调控元件”(NREs)。沉默子元件是经典的、位置独立的元件,指导一种主动抑制机制,而NREs是位置依赖的元件,指导一种被动抑制机制。此外,“阻遏物”是与沉默子直接相互作用的DNA结合转录因子。对近期文献的综述表明,决定抑制机制的是沉默子本身及其在给定启动子中的背景,而非相互作用的阻遏物。沉默子是许多真核生物启动子的固有组成部分,因此,了解它们与增强子及其他转录元件的相互作用对于我们理解真核生物中的基因调控至关重要。