基于CRISPR靶标的单导RNA (sgRNA)用于乙型肝炎病毒诊断检测

J. Christian, Hartiyowidi Yuliawuri, Edvan Arifsaputra Suherman
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摘要

背景:印度尼西亚是东南亚地区乙型肝炎病例第二高的国家。聚集规律间隔短回文重复序列(CRISPR)-CRISPR相关蛋白12 (Cas12)可作为检测乙型肝炎感染的诊断工具。本研究旨在通过设计基于CRISPR靶标的单导RNA (sgRNA),建立一种乙型肝炎病毒的诊断方法。材料与方法:乙型肝炎病毒的preore / core基因序列从美国国家生物技术信息中心(NCBI)网站上收集。选择的序列提交Cas Designer和CRISPOR工具设计sgRNA。利用Benchling软件将得到的sgRNA在计算机上克隆到表达载体中。结果:23个核苷酸序列5'- GTAGTCAGTTATGTCAATGTTAA-3 '的GC含量为30%,帧外68.3,预测效率为76。根据分析,该序列没有错配。结论:这项初步研究将有助于设计一种基于crispr的印度尼西亚乙型肝炎病毒检测诊断试剂盒。然而,需要进一步的体外和体内研究来证明其潜力和效率。关键词:CRISPR-Cas12b,诊断,HBV, sgRNA
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CRISPR Target-based Single-guide RNA (sgRNA) for Diagnostic Testing of Hepatitis B Virus
Background: Indonesia is the second-highest country with hepatitis B cases in the South East Asian region. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated protein 12 (Cas12) could be developed as a diagnostic tool to detect hepatitis B infection. This study was aimed to develop a diagnostic method for hepatitis B virus by designing CRISPR target-based single-guide RNA (sgRNA).Materials and method: The preCore/Core-gene sequences of hepatitis B virus were collected from the National Center for Biotechnology Information (NCBI) website. The selected sequence was submitted to Cas Designer and CRISPOR tools to design sgRNA. The resulting sgRNA was cloned in silico into an expression vector using Benchling software.Results: The 23-nucleotide sequence 5'- GTAGTCAGTTATGTCAATGTTAA-3’ had 30% GC content, 68.3 out-of-frame and 76 predicted efficiencies. This sequence had no mismatch based on analysis.Conclusion: This preliminary study will help design a CRISPR-based diagnostic kit for the detection of hepatitis B virus in Indonesia. However, further in vitro and in vivo studies are required to demonstrate its potential and efficiency.Keywords: CRISPR-Cas12b, diagnostic, HBV, sgRNA 
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