Institut Jacques Monod, Centre National de la Recherche Scientifique, UMR 7592, Université Paris Diderot, Sorbonne Paris Cité, 75205 Paris, France; Université Paris Saclay, Ecole doctorale Structure et Dynamique des Systèmes Vivants, 91190 Gif sur Yvette, France.
Institut Jacques Monod, Centre National de la Recherche Scientifique, UMR 7592, Université Paris Diderot, Sorbonne Paris Cité, 75205 Paris, France.
Mol Cell. 2018 Dec 20;72(6):955-969.e7. doi: 10.1016/j.molcel.2018.11.037.
The fidelity of transcription initiation is essential for accurate gene expression, but the determinants of start site selection are not fully understood. Rap1 and other general regulatory factors (GRFs) control the expression of many genes in yeast. We show that depletion of these factors induces widespread ectopic transcription initiation within promoters. This generates many novel non-coding RNAs and transcript isoforms with diverse stability, drastically altering the coding potential of the transcriptome. Ectopic transcription initiation strongly correlates with altered nucleosome positioning. We provide evidence that Rap1 can suppress ectopic initiation by a "place-holder" mechanism whereby it physically occludes inappropriate sites for pre-initiation complex formation. These results reveal an essential role for GRFs in the fidelity of transcription initiation and in the suppression of pervasive transcription, profoundly redefining current models for their function. They have important implications for the mechanism of transcription initiation and the control of gene expression.
转录起始的保真度对于准确的基因表达至关重要,但启动子选择的决定因素尚不完全清楚。Rap1 和其他一般调控因子 (GRF) 控制着酵母中许多基因的表达。我们发现,这些因子的耗竭会诱导启动子内广泛的异位转录起始。这会产生许多新的非编码 RNA 和具有不同稳定性的转录异构体,从而极大地改变转录组的编码潜力。异位转录起始与核小体定位的改变密切相关。我们提供的证据表明,Rap1 可以通过“占位”机制抑制异位起始,通过该机制,它物理上阻止了不适合预起始复合物形成的不合适位点。这些结果揭示了 GRF 在转录起始保真度和广泛转录抑制中的重要作用,这极大地重新定义了它们功能的现有模型。它们对转录起始机制和基因表达控制具有重要意义。