Worcester Michael, Manoj Femila, Kuhlman Thomas E
Department of Physics and Astronomy, University of California.
Department of Physics and Astronomy, University of California; Microbiology Program, University of California.
J Vis Exp. 2023 Jan 20(191). doi: 10.3791/64825.
Here, a protocol is outlined to perform live, real-time imaging of transposable element activity in live bacterial cells using a suite of fluorescent reporters coupled to transposition. In particular, it demonstrates how real-time imaging can be used to assess the effects of the accessory protein TnpB on the activity of the transposable element IS608, a member of the IS200/IS605 family of transposable elements. The IS200/IS605 family of transposable elements are abundant mobile elements connected with one of the most innumerable genes found in nature, tnpB. Sequence homologies propose that the TnpB protein may be an evolutionary precursor to CRISPR/Cas9 systems. Additionally, TnpB has received renewed interest, having been shown to act as a Cas-like RNA-guided DNA endonuclease. The effects of TnpB on the transposition rates of IS608 are quantified, and it is demonstrated that the expression of TnpB of IS608 results in ~5x increased transposon activity compared to cells lacking TnpB expression.
本文概述了一种方案,该方案使用一套与转座偶联的荧光报告基因,对活细菌细胞中转座元件的活性进行实时成像。特别地,它展示了如何利用实时成像来评估辅助蛋白TnpB对转座元件IS608活性的影响,IS608是IS200/IS605转座元件家族的成员。IS200/IS605转座元件家族是丰富的可移动元件,与自然界中发现的数量最多的基因之一tnpB相关。序列同源性表明,TnpB蛋白可能是CRISPR/Cas9系统的进化前体。此外,TnpB最近重新受到关注,已被证明可作为一种类似Cas的RNA引导的DNA内切酶。对TnpB对IS608转座率的影响进行了量化,结果表明,与缺乏TnpB表达的细胞相比,IS608的TnpB表达导致转座子活性增加约5倍。