Department of Functional Genomics, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS UMR 7104, INSERM U 964, Université de Strasbourg, Illkirch, France.
Trends Biochem Sci. 2010 Jun;35(6):309-14. doi: 10.1016/j.tibs.2010.01.007. Epub 2010 Feb 21.
Early work established the TATA box as the predominant DNA element of core promoters which directed accurate transcription initiation by RNA polymerase II. This element is recognized by TATA-binding protein (TBP), the central DNA-binding subunit of TFIID. In vitro binding and structural experiments indicate that TBP has a strong preference for TATA and induces severe DNA bending. Recent in vivo studies in Saccharomyces cerevisiae indicate that TBP turnover is higher at TATA-containing than at TATA-less promoters; this turnover seems to be regulated by NC2 and Mot1p. We propose that bending of TATA by TBP acts in synergy with NC2 and Mot1p to release TBP more rapidly from TATA promoters in vivo, thus providing a rationale for the predominance of TATA boxes in highly regulated promoters versus constitutively active TATA-less promoters.
早期的工作确立了 TATA 盒作为核心启动子的主要 DNA 元件,指导 RNA 聚合酶 II 进行准确的转录起始。该元件被 TATA 结合蛋白 (TBP) 识别,TBP 是 TFIID 的中心 DNA 结合亚基。体外结合和结构实验表明,TBP 对 TATA 有很强的偏好,并诱导严重的 DNA 弯曲。最近在酿酒酵母中的体内研究表明,与 TATA 缺失启动子相比,TBP 在含有 TATA 的启动子上的周转率更高;这种周转率似乎受 NC2 和 Mot1p 的调节。我们提出,TBP 对 TATA 的弯曲与 NC2 和 Mot1p 协同作用,使 TBP 更迅速地从体内 TATA 启动子上释放,从而为高度调控的启动子中 TATA 盒的优势提供了依据,而 TATA 盒在组成型活性的 TATA 缺失启动子中则较少见。