The Future of Decoding Non-Standard Nucleotides: Leveraging Nanopore Sequencing for Expanded Genetic Codes

Hyunjin Shim
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Abstract

Expanding genetic codes from natural standard nucleotides to artificial non-standard nucleotides marks a significant advancement in synthetic biology, with profound implications for biotechnology and medicine. Decoding the biological information encoded in these non-standard nucleotides presents new challenges, as traditional sequencing technologies are unable to recognize or interpret novel base pairings. In this perspective, we explore the potential of nanopore sequencing, which is uniquely suited to decipher both standard and non-standard nucleotides by directly measuring the biophysical properties of nucleic acids. Nanopore technology offers real-time, long-read sequencing without the need for amplification or synthesis, making it particularly advantageous for expanded genetic systems like Artificially Expanded Genetic Information Systems (AEGIS). We discuss how the adaptability of nanopore sequencing and advancements in data processing can unlock the potential of these synthetic genomes and open new frontiers in understanding and utilizing expanded genetic codes.
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解码非标准核苷酸的未来:利用纳米孔测序扩展遗传密码
将遗传密码从天然标准核苷酸扩展到人工非标准核苷酸标志着合成生物学的重大进展,对生物技术和医学有着深远的影响。解码这些非标准核苷酸编码的生物信息带来了新的挑战,因为传统的测序技术无法识别或解读新型碱基配对。在这一视角中,我们探讨了纳米孔测序技术的潜力,该技术通过直接测量核酸的生物物理特性,在破译标准核苷酸和非标准核苷酸方面具有独特的优势。纳米孔技术提供实时长读数测序,无需扩增或合成,因此对人工扩增遗传信息系统(AEGIS)等扩增遗传系统特别有利。我们将讨论纳米孔测序的适应性和数据处理的进步如何释放这些合成基因组的潜力,并为理解和利用扩展遗传密码开辟新的前沿。
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