Approaches to study CRISPR RNA biogenesis and the key players involved

•crRNA biogenesis relies on diverse endoribonucleases depending on the system.•Most CRISPR-Cas systems employ dedicated, specialized Cas nucleases such as Cas6.•Some systems use cellular host-encoded endoribonucleases, e.g. RNase III or RNase E.•High throughput techniques and molecular methods allow...

Full description

Saved in:
Bibliographic Details
Published inMethods (San Diego, Calif.) Vol. 172; pp. 12 - 26
Main Authors Behler, Juliane, Hess, Wolfgang R.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.02.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•crRNA biogenesis relies on diverse endoribonucleases depending on the system.•Most CRISPR-Cas systems employ dedicated, specialized Cas nucleases such as Cas6.•Some systems use cellular host-encoded endoribonucleases, e.g. RNase III or RNase E.•High throughput techniques and molecular methods allow the identification of crRNAs.•Biochemical and genetic methods are used to characterize crRNA processing nucleases. Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins provide an inheritable and adaptive immune system against phages and foreign genetic elements in many bacteria and archaea. The three stages of CRISPR-Cas immunity comprise adaptation, CRISPR RNA (crRNA) biogenesis and interference. The maturation of the pre-crRNA into mature crRNAs, short guide RNAs that target invading nucleic acids, is crucial for the functionality of CRISPR-Cas defense systems. Mature crRNAs assemble with Cas proteins into the ribonucleoprotein (RNP) effector complex and guide the Cas nucleases to the cognate foreign DNA or RNA target. Experimental approaches to characterize these crRNAs, the specific steps toward their maturation and the involved factors, include RNA-seq analyses, enzyme assays, methods such as cryo-electron microscopy, the crystallization of proteins, or UV-induced protein-RNA crosslinking coupled to mass spectrometry analysis. Complex and multiple interactions exist between CRISPR-cas-encoded specific riboendonucleases such as Cas6, Cas5d and Csf5, endonucleases with dual functions in maturation and interference such as the enzymes of the Cas12 and Cas13 families, and nucleases belonging to the cell’s degradosome such as RNase E, PNPase and RNase J, both in the maturation as well as in interference. The results of these studies have yielded a picture of unprecedented diversity of sequences, enzymes and biochemical mechanisms.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:1046-2023
1095-9130
DOI:10.1016/j.ymeth.2019.07.015