Taurida Academy, V.I. Vernadsky Crimean Federal University, Vernadsky Avenue 4, 295007 Simferopol, Crimea.
Medical Academy named after S.I. Georgievsky, V.I. Vernadsky Crimean Federal University, Lenin Avenue 5/7, 295051 Simferopol, Crimea.
Molecules. 2018 May 29;23(6):1302. doi: 10.3390/molecules23061302.
Antisense oligonucleotides (ASO), short single-stranded polymers based on DNA or RNA chemistries and synthesized in vitro, regulate gene expression by binding in a sequence-specific manner to an RNA target. The functional activity and selectivity in the action of ASOs largely depends on the combination of nitrogenous bases in a target sequence. This simple and natural property of nucleic acids provides an attractive route by which scientists can create different ASO-based techniques. Over the last 50 years, planned and realized applications in the field of antisense and nucleic acid nanotechnologies have produced astonishing results and posed new challenges for further developments, exemplifying the essence of the post-genomic era. Today the majority of ASOs are chemically modified and/or incorporated within nanoparticles to enhance their stability and cellular uptake. This review critically analyzes some successful cases using the antisense approach in medicine to address severe diseases, such as Duchenne muscular dystrophy and spinal muscular atrophy, and suggests some prospective directions for future research. We also examine in detail the elaboration of unmodified insect-specific DNA insecticides and RNA preparations in the areas of agriculture and forestry, a relatively new branch of ASO that allows circumvention of the use of non-selective chemical insecticides. When considering the variety of successful ASO modifications with an efficient signal-to-noise ratio of action, coupled with the affordability of in vitro oligonucleotide synthesis and post-synthesis procedures, we predict that the next half-century will produce a fruitful yield of tools created from effective ASO-based end products.
反义寡核苷酸(ASO)是基于 DNA 或 RNA 化学合成的短单链聚合物,通过与 RNA 靶标以序列特异性方式结合来调节基因表达。ASO 的功能活性和作用选择性在很大程度上取决于靶序列中含氮碱基的组合。核酸的这种简单而自然的特性为科学家提供了一种有吸引力的途径,可以创建不同的基于 ASO 的技术。在过去的 50 年中,反义技术和核酸纳米技术领域中计划和实现的应用取得了惊人的成果,并为进一步的发展提出了新的挑战,体现了后基因组时代的本质。如今,大多数 ASO 都经过化学修饰和/或包含在纳米颗粒中,以提高其稳定性和细胞摄取能力。本综述批判性地分析了一些成功案例,这些案例使用反义方法在医学上治疗严重疾病,如杜氏肌营养不良症和脊髓性肌萎缩症,并为未来的研究提出了一些前瞻性方向。我们还详细研究了在农业和林业领域中未修饰的昆虫特异性 DNA 杀虫剂和 RNA 制剂的详细阐述,这是 ASO 的一个相对较新的分支,它允许规避使用非选择性化学杀虫剂。考虑到具有高效信号噪声比的多种成功 ASO 修饰,再加上体外寡核苷酸合成和合成后程序的可负担性,我们预测,下一个半世纪将产生丰富的基于有效 ASO 的最终产品的工具。