Hendrix David A, Hong Joung-Woo, Zeitlinger Julia, Rokhsar Daniel S, Levine Michael S
Department Molecular and Cell Biology, Division of Genetics, Genomics, and Development, Center for Integrative Genomics, University of California, Berkeley, CA 94720, USA.
Proc Natl Acad Sci U S A. 2008 Jun 3;105(22):7762-7. doi: 10.1073/pnas.0802406105. Epub 2008 May 27.
RNA Polymerase II (Pol II) is bound to the promoter regions of many or most developmental control genes before their activation during Drosophila embryogenesis. It has been suggested that Pol II stalling is used to produce dynamic and rapid responses of developmental patterning genes to transient cues such as extracellular signaling molecules. Here, we present a combined computational and experimental analysis of stalled promoters to determine how they come to bind Pol II in the early Drosophila embryo. At least one-fourth of the stalled promoters contain a shared sequence motif, the "pause button" (PB): KCGRWCG. The PB motif is sometimes located in the position of the DPE, and over one-fifth of the stalled promoters contain the following arrangement of core elements: GAGA, Inr, PB, and/or DPE. This arrangement was used to identify additional stalled promoters in the Drosophila genome, and permanganate footprint assays were used to confirm that the segmentation gene engrailed contains paused Pol II as seen for heat-shock genes. We discuss different models for Pol II binding and gene activation in the early embryo.
在果蝇胚胎发育过程中,许多或大多数发育控制基因在激活之前,RNA聚合酶II(Pol II)就已结合在其启动子区域。有人提出,Pol II停滞用于使发育模式基因对诸如细胞外信号分子等瞬时信号产生动态快速反应。在此,我们对停滞的启动子进行了计算与实验相结合的分析,以确定它们在果蝇早期胚胎中是如何结合Pol II的。至少四分之一的停滞启动子含有一个共享序列基序,即“暂停按钮”(PB):KCGRWCG。PB基序有时位于DPE的位置,超过五分之一的停滞启动子含有以下核心元件排列:GAGA、起始子(Inr)、PB和/或DPE。这种排列被用于在果蝇基因组中识别其他停滞启动子,高锰酸盐足迹分析被用于证实,如热休克基因一样,体节基因engrailed含有暂停的Pol II。我们讨论了早期胚胎中Pol II结合和基因激活的不同模型。