Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Dokl Biochem Biophys. 2022 Oct;506(1):210-214. doi: 10.1134/S1607672922050039. Epub 2022 Oct 27.
Polycomb group (PcG) repressors and Trithorax group (TrxG) activators of transcription are essential for the proper development and maintenance of gene expression profiles in multicellular organisms. In Drosophila, PcG/TrxG proteins interact with DNA elements called PRE (Polycomb response elements). We have previously shown that the repressive activity of inactive PRE in transgenes can be induced by architectural protein-binding sites. It was shown that the induction of repression is associated with the recruitment of PcG/TrxG proteins, including the DNA-binding factors Pho and Combgap. In the present study, we tested the association of the two other PRE DNA-binding factors, GAF and Psq, with bxdPRE in the presence and absence of sites for architectural proteins. As a result, it was shown that both factors can be efficiently recruited to the bxdPRE only in the presence of adjacent binding sites for architectural proteins Su(Hw), CTCF, or Pita.
多梳组(PcG)抑制因子和转录的三翼螺旋组(TrxG)激活因子对于多细胞生物中基因表达谱的正常发育和维持是必不可少的。在果蝇中,PcG/TrxG 蛋白与称为 PRE(多梳反应元件)的 DNA 元件相互作用。我们之前已经表明,转座基因中无活性 PRE 的抑制活性可以通过结构蛋白结合位点诱导。研究表明,抑制的诱导与 PcG/TrxG 蛋白的募集有关,包括 DNA 结合因子 Pho 和 Combgap。在本研究中,我们测试了另外两个 PRE DNA 结合因子 GAF 和 Psq 在存在和不存在结构蛋白结合位点的情况下与 bxdPRE 的关联。结果表明,只有在存在相邻的结构蛋白 Su(Hw)、CTCF 或 Pita 结合位点的情况下,这两个因子才能有效地被招募到 bxdPRE。