Ainbinder Elena, Amir-Zilberstein Liat, Yamaguchi Yuki, Handa Hiroshi, Dikstein Rivka
Department of Biological Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel.
Mol Cell Biol. 2004 Mar;24(6):2444-54. doi: 10.1128/MCB.24.6.2444-2454.2004.
A20 is an immediate-early NF-kappaB target gene. Prior to NF-kappaB stimulation, the A20 promoter is bound by the polymerase II machinery to allow rapid transcription activation. Here we show that the basal A20 transcription is repressed at the level of elongation in a promoter-specific fashion. Immunodepletion in vitro and RNA interference in cultured cells suggest that the basal elongation inhibition is conferred by DRB sensitivity-inducing factor (DSIF). We have identified a negative upstream promoter element called ELIE that controls DSIF activity. Remarkably, following NF-kappaB stimulation, inhibition of the A20 promoter by DSIF persists, but it is now regulated by NF-kappaB rather than ELIE. Similar regulation by DSIF is shown for another NF-kappaB-responsive gene, the IkappaBalpha gene. These findings reveal an intimate and dynamic relationship between DSIF inhibition of elongation and promoter-bound transcription factors. The potential significance of the differential regulation of DSIF activity by cis-acting elements is discussed.
A20是一种即刻早期核因子κB(NF-κB)靶基因。在NF-κB激活之前,A20启动子与聚合酶II机制结合,以实现快速转录激活。在此我们表明,基础A20转录在延伸水平以启动子特异性方式受到抑制。体外免疫去除和培养细胞中的RNA干扰表明,基础延伸抑制由DRB敏感性诱导因子(DSIF)介导。我们鉴定出一个名为ELIE的负性上游启动子元件,它控制DSIF活性。值得注意的是,在NF-κB激活后,DSIF对A20启动子的抑制持续存在,但此时它由NF-κB而非ELIE调控。另一个NF-κB反应基因IkappaBalpha基因也显示出由DSIF进行的类似调控。这些发现揭示了DSIF对延伸的抑制与启动子结合转录因子之间密切且动态的关系。我们还讨论了顺式作用元件对DSIF活性进行差异调控的潜在意义。