AUTHOR=Filippova Julia A. , Matveeva Anastasiya M. , Zhuravlev Evgenii S. , Balakhonova Evgenia A. , Prokhorova Daria V. , Malanin Sergey J. , Shah Mahmud Raihan , Grigoryeva Tatiana V. , Anufrieva Ksenia S. , Semenov Dmitry V. , Vlassov Valentin V. , Stepanov Grigory A. TITLE=Are Small Nucleolar RNAs “CRISPRable”? A Report on Box C/D Small Nucleolar RNA Editing in Human Cells JOURNAL=Frontiers in Pharmacology VOLUME=10 YEAR=2019 URL=https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.01246 DOI=10.3389/fphar.2019.01246 ISSN=1663-9812 ABSTRACT=
CRISPR technologies are nowadays widely used for targeted knockout of numerous protein-coding genes and for the study of various processes and metabolic pathways in human cells. Most attention in the genome editing field is now focused on the cleavage of protein-coding genes or genes encoding long non-coding RNAs (lncRNAs), while the studies on targeted knockout of intron-encoded regulatory RNAs are sparse. Small nucleolar RNAs (snoRNAs) present a class of non-coding RNAs encoded within the introns of various host genes and involved in post-transcriptional maturation of ribosomal RNAs (rRNAs) in eukaryotic cells. Box C/D snoRNAs direct 2’-O-methylation of rRNA nucleotides. These short RNAs have specific elements in their structure, namely, boxes C and D, and a target-recognizing region. Here, we present the study devoted to CRISPR/Cas9-mediated editing of box C/D snoRNA genes in