Munshi Rahul, Ling Jia, Ryabichko Sergey, Wieschaus Eric F, Gregor Thomas
Joseph Henry Laboratories of Physics, Princeton University, Princeton, NJ 08544, USA.
Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Sci Adv. 2025 Jan 3;11(1):eadp3251. doi: 10.1126/sciadv.adp3251. Epub 2025 Jan 1.
Deciphering how genes interpret information from transcription factor (TF) concentrations within the cell nucleus remains a fundamental question in gene regulation. Recent advancements have revealed the heterogeneous distribution of TF molecules, posing challenges to precisely decoding concentration signals. Using high-resolution single-cell imaging of the fluorescently tagged TF Bicoid in living embryos, we show that Bicoid accumulation in submicrometer clusters preserves the spatial information of the maternal Bicoid gradient. These clusters provide precise spatial cues through intensity, size, and frequency. We further discover that Bicoid target genes colocalize with these clusters in an enhancer-binding affinity-dependent manner. Our modeling suggests that clustering offers a faster sensing mechanism for global nuclear concentrations than freely diffusing TF molecules detected by simple enhancers.
解读基因如何解读来自细胞核内转录因子(TF)浓度的信息仍然是基因调控中的一个基本问题。最近的进展揭示了TF分子的异质分布,对精确解码浓度信号提出了挑战。通过对活胚胎中荧光标记的TF双尾进行高分辨率单细胞成像,我们发现双尾在亚微米级聚集体中的积累保留了母体双尾梯度的空间信息。这些聚集体通过强度、大小和频率提供精确的空间线索。我们进一步发现,双尾靶基因以增强子结合亲和力依赖的方式与这些聚集体共定位。我们的模型表明,与简单增强子检测到的自由扩散TF分子相比,聚集体为全局核浓度提供了一种更快的传感机制。