دورية أكاديمية

CRISPR-Cas12a exploits R-loop asymmetry to form double-strand breaks

التفاصيل البيبلوغرافية
العنوان: CRISPR-Cas12a exploits R-loop asymmetry to form double-strand breaks
المؤلفون: Cofsky, Joshua C, Karandur, Deepti, Huang, Carolyn J, Witte, Isaac P, Kuriyan, John, Doudna, Jennifer A
المساهمون: Howard Hughes Medical Institute, National Science Foundation
المصدر: eLife ; volume 9 ; ISSN 2050-084X
بيانات النشر: eLife Sciences Publications, Ltd
سنة النشر: 2020
المجموعة: eLife (E-Journal - via CrossRef)
الوصف: Type V CRISPR-Cas interference proteins use a single RuvC active site to make RNA-guided breaks in double-stranded DNA substrates, an activity essential for both bacterial immunity and genome editing. The best-studied of these enzymes, Cas12a, initiates DNA cutting by forming a 20-nucleotide R-loop in which the guide RNA displaces one strand of a double-helical DNA substrate, positioning the DNase active site for first-strand cleavage. However, crystal structures and biochemical data have not explained how the second strand is cut to complete the double-strand break. Here, we detect intrinsic instability in DNA flanking the RNA-3′ side of R-loops, which Cas12a can exploit to expose second-strand DNA for cutting. Interestingly, DNA flanking the RNA-5′ side of R-loops is not intrinsically unstable. This asymmetry in R-loop structure may explain the uniformity of guide RNA architecture and the single-active-site cleavage mechanism that are fundamental features of all type V CRISPR-Cas systems.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.7554/elife.55143
الإتاحة: https://doi.org/10.7554/elife.55143Test
https://cdn.elifesciences.org/articles/55143/elife-55143-v2.pdfTest
https://cdn.elifesciences.org/articles/55143/elife-55143-v2.xmlTest
https://elifesciences.org/articles/55143Test
حقوق: http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.C3378865
قاعدة البيانات: BASE
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