Depken Martin, Galburt Eric A, Grill Stephan W
Max Planck Institute for the Physics of Complex Systems, Dresden, Germany.
Biophys J. 2009 Mar 18;96(6):2189-93. doi: 10.1016/j.bpj.2008.12.3918.
RNA polymerases are protein molecular machines that transcribe genetic information from DNA into RNA. The elongation of the RNA molecule is frequently interrupted by pauses, the detailed nature of which remains controversial. Here we ask whether backtracking, the central mechanism behind long pauses, could also be responsible for short pauses normally attributed to the ubiquitous pause state. To this end, we model backtracking as a force-biased random walk, giving rise to a broad distribution of pause durations as observed in experiments. Importantly, we find that this single mechanism naturally generates two populations of pauses that are distinct both in duration and trajectory: long-time pauses with the expected behavior of diffusive backtracks, and a new class of short-time backtracks with characteristics similar to those of the ubiquitous pause. These characteristics include an apparent force insensitivity and immobility of the polymerase. Based on these results and a quantitative comparison to published pause trajectories measured with optical tweezers, we suggest that a significant fraction of short pauses are simply due to backtracking.
RNA聚合酶是将遗传信息从DNA转录为RNA的蛋白质分子机器。RNA分子的延伸常常被暂停打断,其详细性质仍存在争议。在这里,我们探讨长暂停背后的核心机制——回溯,是否也能解释通常归因于普遍存在的暂停状态的短暂停。为此,我们将回溯建模为一种力偏置随机游走,从而产生实验中观察到的广泛的暂停持续时间分布。重要的是,我们发现这一单一机制自然地产生了两类在持续时间和轨迹上都不同的暂停:具有扩散性回溯预期行为的长时间暂停,以及一类新的具有与普遍存在的暂停相似特征的短时间回溯。这些特征包括聚合酶明显的力不敏感性和不动性。基于这些结果以及与用光学镊子测量的已发表的暂停轨迹的定量比较,我们认为相当一部分短暂停仅仅是由于回溯造成的。