Elizar'ev P V, Lomaev D V, Chetverina D A, Georgiev P G, Erokhin M M
Institute of Gene Biology, Russian Academy of Sciences, Vavilov str. 34/5, 119334, Moscow, Russia.
Acta Naturae. 2016 Apr-Jun;8(2):79-86.
Maintenance of the individual patterns of gene expression in different cell types is required for the differentiation and development of multicellular organisms. Expression of many genes is controlled by Polycomb (PcG) and Trithorax (TrxG) group proteins that act through association with chromatin. PcG/TrxG are assembled on the DNA sequences termed PREs (Polycomb Response Elements), the activity of which can be modulated and switched from repression to activation. In this study, we analyzed the influence of transcriptional read-through on PRE activity switch mediated by the yeast activator GAL4. We show that a transcription terminator inserted between the promoter and PRE doesn't prevent switching of PRE activity from repression to activation. We demonstrate that, independently of PRE orientation, high levels of transcription fail to dislodge PcG/TrxG proteins from PRE in the absence of a terminator. Thus, transcription is not the main factor required for PRE activity switch.
多细胞生物体的分化和发育需要维持不同细胞类型中基因表达的个体模式。许多基因的表达受多梳(PcG)和三胸(TrxG)蛋白家族控制,这些蛋白通过与染色质结合发挥作用。PcG/TrxG组装在称为PREs(多梳反应元件)的DNA序列上,其活性可以被调节并从抑制转换为激活。在本研究中,我们分析了转录通读对酵母激活因子GAL4介导的PRE活性转换的影响。我们发现,插入启动子和PRE之间的转录终止子并不能阻止PRE活性从抑制转换为激活。我们证明,在没有终止子的情况下,无论PRE的方向如何,高水平的转录都无法将PcG/TrxG蛋白从PRE上移除。因此,转录不是PRE活性转换所需的主要因素。