Department of Biochemistry and Molecular Biology, Yamaguchi University School of Medicine, Ube, Japan.
FEBS Lett. 2023 Jul;597(13):1702-1717. doi: 10.1002/1873-3468.14617. Epub 2023 Apr 4.
Upon heat shock, activated heat shock transcription factor 1 (HSF1) binds to the heat shock response elements (HSEs) in the promoters of mammalian heat shock protein (HSP)-encoding genes and recruits the preinitiation complex and coactivators, including Mediator. These transcriptional regulators may be concentrated in phase-separated condensates around the promoters, but they are too minute to be characterized in detail. We herein established HSF1 mouse embryonic fibroblasts harbouring HSP72-derived multiple HSE arrays and visualized the condensates of fluorescent protein-tagged HSF1 with liquid-like properties upon heat shock. Using this experimental system, we demonstrate that endogenous MED12, a subunit of Mediator, is concentrated in artificial HSF1 condensates upon heat shock. Furthermore, the knockdown of MED12 markedly reduces the size of condensates, suggesting an important role for MED12 in HSF1 condensate formation.
热休克后,激活的热休克转录因子 1(HSF1)与哺乳动物热休克蛋白(HSP)编码基因启动子中的热休克反应元件(HSE)结合,并募集起始复合物和共激活因子,包括中介体。这些转录调节剂可能集中在启动子周围相分离的液滴中,但由于它们太小,无法详细描述。我们在此建立了携带 HSP72 衍生的多个 HSE 阵列的 HSF1 小鼠胚胎成纤维细胞,并在热休克下可视化具有液态特性的荧光蛋白标记的 HSF1 的液滴。使用这个实验系统,我们证明了内源性 MED12(中介体的一个亚基)在热休克时集中在人工 HSF1 液滴中。此外,MED12 的敲低显著减小了液滴的大小,表明 MED12 在 HSF1 液滴形成中起着重要作用。