Flores Eduardo, Camacho Aleah R, Cuevas-Zepeda Estefania, McCoy Mary B, Yu Feng, Staller Max V, Sukenik Shahar
Department of Chemistry and Biochemistry, University of California, Merced, Merced, California.
Department of Chemistry and Biochemistry, University of California, Merced, Merced, California; Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, California.
Biophys Rep (N Y). 2025 Mar 12;5(1):100195. doi: 10.1016/j.bpr.2024.100195. Epub 2025 Jan 3.
Transcription factor proteins bind to specific DNA promoter sequences and initiate gene transcription. These proteins often contain intrinsically disordered activation domains (ADs) that regulate their transcriptional activity. Like other disordered protein regions, ADs do not have a fixed three-dimensional structure and instead exist in an ensemble of conformations. Disordered ensembles contain sequence-encoded structural preferences that are often linked to their function. We hypothesize that this link exists between the structural preferences of AD ensembles and their ability to induce gene expression. To test this, we measured the ensemble dimensions of two ADs, HIF-1α and CITED2, in live cells using fluorescence resonance energy transfer microscopy and correlated this structural information with their transcriptional activity. We find that mutations that expanded the ensemble of HIF-1α increased transcriptional activity, while compacting mutations reduced it, highlighting the critical role of structural plasticity in regulating HIF-1α function. Conversely, CITED2 showed no correlation between ensemble dimensions and activity. Our results highlight a possible link between AD ensemble dimensions and their transcriptional activity, with implications for transcriptional regulation and dysfunction.
转录因子蛋白与特定的DNA启动子序列结合并启动基因转录。这些蛋白质通常含有调节其转录活性的内在无序激活域(ADs)。与其他无序蛋白质区域一样,ADs没有固定的三维结构,而是以一系列构象存在。无序集合包含通常与其功能相关的序列编码结构偏好。我们假设AD集合的结构偏好与其诱导基因表达的能力之间存在这种联系。为了验证这一点,我们使用荧光共振能量转移显微镜测量了活细胞中两种ADs(缺氧诱导因子-1α(HIF-1α)和CITED2)的集合尺寸,并将这种结构信息与其转录活性相关联。我们发现,扩展HIF-1α集合的突变增加了转录活性,而压缩突变则降低了转录活性,突出了结构可塑性在调节HIF-1α功能中的关键作用。相反,CITED2的集合尺寸与活性之间没有相关性。我们的结果突出了AD集合尺寸与其转录活性之间的可能联系,对转录调控和功能障碍具有重要意义。