The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Programmable RNA detection with CRISPR-Cas12a
Open accessAbstract
Cas12a, a CRISPR-associated protein complex, has an inherent ability to cleave DNA substrates and is utilized in diagnostic tools to identify DNA molecules. We demonstrate that multiple orthologs of Cas12a activate trans-cleavage in the presence of split activators. Specifically, the PAM-distal region of the crRNA recognizes RNA targets provided that the PAM-proximal seed region has a DNA target. Our method, Split Activator for Highly Accessible RNA Analysis (SAHARA), detects picomolar concentrations of RNA without sample amplification, reverse-transcription, or strand-displacement by simply supplying a short DNA sequence complementary to the seed region. Beyond RNA detection, SAHARA outperforms wild-type CRISPR-Cas12a in specificity towards point-mutations and can detect multiple RNA and DNA targets in pooled crRNA/Cas12a arrays via distinct PAM-proximal seed DNAs. In conclusion, SAHARA is a simple, yet powerful nucleic acid detection platform based on Cas12a that can be applied in a multiplexed fashion and potentially be expanded to other CRISPR-Cas enzymes.
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A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity
Jinek, M., Chylinski, K., Fonfara, I., Hauer, M., Doudna, J. A., & Charpentier, E. (2012) · Science · doi:10.1126/science.1225829 · Cited by 17,116
Deciphering key features in protein structures with the new ENDscript server
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CRISPR Provides Acquired Resistance Against Viruses in Prokaryotes
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Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System
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CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity
Chen, J. S., Ma, E., Harrington, L. B., Da Costa, M., Tian, X., Palefsky, J. M., & Doudna, J. A. (2018) · Science · doi:10.1126/science.aar6245 · Cited by 4,507
MicroRNA Gene Expression Deregulation in Human Breast Cancer
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Nucleic acid detection with CRISPR-Cas13a/C2c2
Gootenberg, J. S., Abudayyeh, O. O., Lee, J. W., Essletzbichler, P., Dy, A. J., Joung, J., Verdine, V., Donghia, N., Daringer, N. M., Freije, C. A., et al. (2017) · Science · doi:10.1126/science.aam9321 · Cited by 3,844
CRISPR–Cas12-based detection of SARS-CoV-2
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Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6
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Small CRISPR RNAs Guide Antiviral Defense in Prokaryotes
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Metadata
- Authors
- Rananaware, S. R., Vesco, E. K., Shoemaker, G. M., Anekar, S. S., Sandoval, L. S. W., Meister, K. S., Macaluso, N. C., Nguyen, L. T., & Jain, P. K.
- Venue
- Nature Communications
- Published
- 2023-09-05
- Volume
- 14
- Issue
- 1
- Pages
- 5409-5409
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W4386440508
- Cited by
- 266
- References
- 54
- FWCI
- 19.88
- Type
- journal article
- Language
- en
- Open access
- gold
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- Rananaware, S. R., Vesco, E. K., Shoemaker, G. M., Anekar, S. S., Sandoval, L. S. W., Meister, K. S., Macaluso, N. C., Nguyen, L. T., & Jain, P. K. (2023). Programmable RNA detection with CRISPR-Cas12a. Nature Communications. https://doi.org/10.1038/s41467-023-41006-1
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