The CRISPR-Cas13a Gemini System for noncontiguous target RNA activation

• Published in: Nature communications Vol. 15; no. 1; p. 2901
• Main Authors: Zhao, Hongrui, Sheng, Yan, Zhang, Tenghua, Zhou, Shujun, Zhu, Yuqing, Qian, Feiyang, Liu, Meiru, Xu, Weixue, Zhang, Dengsong, Hu, Jiaming
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 04.04.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 14/10; 14/19; 14/3; 14/34; 14/35; 38/77; 631/154/140; 631/1647/2196; 631/337/4041; 631/61/32; Biomarkers; Colorimetry; CRISPR; Crystal structure; Diagnosis; Editing; Epstein-Barr virus; Genetic modification; Genome editing; Humanities and Social Sciences; Mammalian cells; miRNA; multidisciplinary; Ribonucleic acid; RNA; Science; Science (multidisciplinary); Target detection; Transgenes
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-024-47281-w

Simultaneous multi-target detection and multi-site gene editing are two key factors restricting the development of disease diagnostic and treatment technologies. Despite numerous explorations on the source, classification, functional features, crystal structure, applications and engineering of CRISPR-Cas13a, all reports use the contiguous target RNA activation paradigm that only enables single-target detection in vitro and one-site gene editing in vivo. Here we propose a noncontiguous target RNA activation paradigm of Cas13a and establish a CRISPR-Cas13a Gemini System composed of two Cas13a:crRNA binary complexes, which can provide rapid, simultaneous, highly specific and sensitive detection of two RNAs in a single readout, as well as parallel dual transgene knockdown. CRISPR-Cas13a Gemini System are demonstrated in the detection of two miRNAs (miR-155 and miR-375) for breast cancer diagnosis and two small RNAs (EBER-1 and EBER-2) for Epstein-Barr virus diagnosis using multiple diagnostic platforms, including fluorescence and colorimetric-based lateral flow systems. We also show that CRISPR-Cas13a Gemini System can knockdown two foreign genes (EGFP and mCherry transcripts) in mammalian cells simultaneously. These findings suggest the potential of highly effective and simultaneous detection of multiple biomarkers and gene editing of multiple sites. CRISPR-Cas13a based methods currently use contiguous target RNA activation, which only enables single-target detection or editing. Here the authors propose a noncontiguous target RNA activation approach which can provide rapid, simultaneous and sensitive detection of two RNAs in a single readout, as well as parallel dual transgene knockdown.