Vinayachandran Vinesh, Bhargava Purnima
Centre for Cellular and Molecular Biology (Council of Scientific and Industrial Research), Hyderabad, India.
Front Genet. 2022 May 13;13:870700. doi: 10.3389/fgene.2022.870700. eCollection 2022.
A small non-histone protein of budding yeast, Nhp6 has been reported to specifically influence the transcription of a yeast gene, . The gene is essential, transcribed by the enzyme RNA polymerase III, and codes for the U6snRNA required for mRNA splicing. A translationally positioned nucleosome on the gene body enables the assembly factor TFIIIC binding by juxtaposing its otherwise widely separated binding sites, boxes A and B. We found histone depletion results in the loss of U6 snRNA production. Changing the rotational phase of the boxes and the linear distance between them with deletions in 5 bp steps displayed a helical periodicity in transcription, which gradually reduced with incremental deletions up to 40 bp but increased on further deletions enclosing the pseudoA boxes. Nhp6 influences the transcription in a dose-dependent manner, which is modulated by its previously reported co-operator, an upstream stretch of seven T residues centered between the TATA box and transcription start site. Nhp6 occupancy on the gene goes up at least 2-fold under the repression conditions. Nhp6 absence, T disruption, or shorter A-B box distance all cause the downstream initiation of transcription. The right +1 site is selected with the correct placement of TFIIIC before the transcription initiation factor TFIIIB. Thus, the T sequence and Nhp6 help the assembly and placement of the transcription complex at the right position. Apart from the chromatin remodelers, the relative rotational orientation of the promoter elements in nucleosomal DNA, and Nhp6 regulate the transcription of the gene with precision.
芽殖酵母的一种小的非组蛋白Nhp6已被报道能特异性影响酵母基因的转录。该基因至关重要,由RNA聚合酶III转录,编码mRNA剪接所需的U6snRNA。基因体上的一个翻译定位核小体通过将其原本广泛分离的结合位点A盒和B盒并列,使组装因子TFIIIC得以结合。我们发现组蛋白缺失会导致U6 snRNA产生的丧失。以5个碱基对的步长进行缺失来改变A盒和B盒的旋转相位及其之间的线性距离,在转录过程中呈现出螺旋周期性,这种周期性随着缺失增加到40个碱基对而逐渐降低,但在进一步缺失包含假A盒时又会增加。Nhp6以剂量依赖的方式影响转录,其转录受先前报道的协同作用因子调节,该协同作用因子是位于TATA盒和转录起始位点之间中心位置的一段七个T残基的上游序列。在抑制条件下,Nhp6在该基因上的占据率至少会增加2倍。Nhp6缺失、T序列破坏或A - B盒距离缩短都会导致转录在下游起始。在转录起始因子TFIIIB之前,通过TFIIIC的正确定位选择了正确的+1位点。因此,T序列和Nhp6有助于转录复合物在正确位置的组装和定位。除了染色质重塑因子外,核小体DNA中启动子元件的相对旋转方向以及Nhp6精确地调节该基因的转录。