Department of Molecular & Cell Biology, UC Berkeley, Berkeley, CA 94720, USA.
Department of Plant and Microbial Biology, UC Berkeley, Berkeley, CA 94720, USA.
Cell. 2018 Jun 14;173(7):1810-1822.e16. doi: 10.1016/j.cell.2018.03.069. Epub 2018 May 10.
Embryonic cell fates are defined by transcription factors that are rapidly deployed, yet attempts to visualize these factors in vivo often fail because of slow fluorescent protein maturation. Here, we pioneer a protein tag, LlamaTag, which circumvents this maturation limit by binding mature fluorescent proteins, making it possible to visualize transcription factor concentration dynamics in live embryos. Implementing this approach in the fruit fly Drosophila melanogaster, we discovered stochastic bursts in the concentration of transcription factors that are correlated with bursts in transcription. We further used LlamaTags to show that the concentration of protein in a given nucleus heavily depends on transcription of that gene in neighboring nuclei; we speculate that this inter-nuclear signaling is an important mechanism for coordinating gene expression to delineate straight and sharp boundaries of gene expression. Thus, LlamaTags now make it possible to visualize the flow of information along the central dogma in live embryos.
胚胎细胞命运由转录因子决定,这些转录因子迅速被募集,但由于荧光蛋白成熟缓慢,尝试在体内可视化这些因子往往会失败。在这里,我们开创了一种蛋白质标签,LlamaTag,它通过结合成熟的荧光蛋白来绕过这种成熟限制,从而使我们能够在活胚胎中可视化转录因子浓度动态。在果蝇 Drosophila melanogaster 中实施这种方法,我们发现转录因子浓度会随机爆发,与转录爆发相关。我们进一步使用 LlamaTags 表明,给定核内的蛋白质浓度在很大程度上取决于相邻核内该基因的转录;我们推测,这种核间信号传递是协调基因表达以描绘基因表达的直线和清晰边界的重要机制。因此,LlamaTags 现在使得在活胚胎中沿着中心法则可视化信息流动成为可能。