Hunan Provincial Key Laboratory of Phytohormones and Growth Development, College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China.
Guangdong Provincial Key Laboratory of Plant Epigenetics, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Molecules. 2021 Oct 25;26(21):6432. doi: 10.3390/molecules26216432.
MicroRNA160 plays a crucial role in plant development by negatively regulating the auxin response factors (ARFs). In this manuscript, we design an automatic molecule machine (AMM) based on the dual catalytic hairpin assembly (D-CHA) strategy for the signal amplification detection of miRNA160. The detection system contains four hairpin-shaped DNA probes (HP1, HP2, HP3, and HP4). For HP1, the loop is designed to be complementary to miRNA160. A fragment of DNA with the same sequences as miRNA160 is separated into two pieces that are connected at the 3' end of HP2 and 5' end of HP3, respectively. In the presence of the target, four HPs are successively dissolved by the first catalytic hairpin assembly (CHA1), forming a four-way DNA junction (F-DJ) that enables the rearrangement of separated DNA fragments at the end of HP2 and HP3 and serving as an integrated target analogue for initiating the second CHA reaction, generating an enhanced fluorescence signal. Assay experiments demonstrate that D-CHA has a better performance compared with traditional CHA, achieving the detection limit as low as 10 pM for miRNA160 as deduced from its corresponding DNA surrogates. Moreover, non-target miRNAs, as well as single-base mutation targets, can be detected. Overall, the D-CHA strategy provides a competitive method for plant miRNAs detection.
miRNA160 通过负调控生长素响应因子(ARFs)在植物发育中发挥着关键作用。在本手稿中,我们设计了一种基于双催化发夹组装(D-CHA)策略的自动分子机器(AMM),用于 miRNA160 的信号放大检测。该检测系统包含四个发夹状 DNA 探针(HP1、HP2、HP3 和 HP4)。对于 HP1,其环设计为与 miRNA160 互补。与 miRNA160 具有相同序列的 DNA 片段被分成两部分,分别连接到 HP2 的 3'端和 HP3 的 5'端。在存在靶标的情况下,四个 HP 首先被第一个催化发夹组装(CHA1)溶解,形成四向 DNA 结(F-DJ),从而使 HP2 和 HP3 末端分离的 DNA 片段重新排列,并作为集成的靶标类似物启动第二个 CHA 反应,产生增强的荧光信号。测定实验表明,与传统的 CHA 相比,D-CHA 具有更好的性能,对于其相应的 DNA 替代物,能够实现低至 10 pM 的 miRNA160 检测限。此外,还可以检测非靶 miRNAs 以及单碱基突变靶标。总的来说,D-CHA 策略为植物 miRNAs 的检测提供了一种有竞争力的方法。