The Mina and Everard Goodman Faculty of Life Sciences and Institute of Nanotechnology, Bar-Ilan University, Ramat Gan, Israel.
Histochem Cell Biol. 2013 Jul;140(1):71-9. doi: 10.1007/s00418-013-1100-2. Epub 2013 Jun 9.
The kinetic aspects of RNA polymerase II as it transcribes mRNA have been revealed over the past decade by use of live-cell imaging and kinetic analyses. It is now possible to visualize polymerase molecules in action, and most importantly to detect and follow the mRNA product as it is generated in real time on active genes. Questions such as the speed at which mRNAs are transcribed or the number of polymerases running along a particular gene can be addressed at high temporal resolution. These kinetic studies highlight the tight regulation that genes encounter when moving between active and inactive states, and ultimately will shed light on the kinetic aspects of transcription of genes under perturbed states. The scientific pathway along which these findings were unearthed begins with the imaging of the action of hundreds of genes working in concert in fixed cells. The state of the art has reached the capability of analyzing the transcription of single alleles in living mammalian cells.
在过去的十年中,通过使用活细胞成像和动力学分析,揭示了 RNA 聚合酶 II 在转录 mRNA 时的动力学方面。现在可以观察到聚合酶分子的作用,更重要的是,可以实时检测和跟踪在活性基因上生成的 mRNA 产物。可以以高时间分辨率解决诸如转录 mRNA 的速度或沿特定基因运行的聚合酶数量等问题。这些动力学研究强调了基因在活跃和不活跃状态之间转换时所遇到的严格调控,并最终将阐明在受干扰状态下基因转录的动力学方面。这些发现的科学途径始于对数百个协同工作的基因在固定细胞中的作用进行成像。最先进的技术已经达到了在活哺乳动物细胞中分析单个等位基因转录的能力。