Kuznedelov, KonstantinMekler, VladimirLemak, SofiaTokmina-Lukaszewska, MonikaDatsenko, Kirill AJain, IshitaSavitskaya, EkaterinaMallon, JohnShmakov, SergeyBothner, BrianBailey, ScottYakunin, Alexander FSeverinov, Konstantin2017-02-142017-02-142016-10Kuznedelov, Konstantin , Vladimir Mekler, Sofia Lemak, Monika Tokmina-Lukaszewska, Kirill A Datsenko, Ishita Jain, Ekaterina Savitskaya, John Mallon, Sergey Shmakov, Brian Bothner, Scott Bailey, Alexander F Yakunin, and Konstantin Severinov. "Altered stoichiometry Escherichia coli Cascade complexes with shortened CRISPR RNA spacers are capable of interference and primed adaptation." Nucleic Acids Research (October 2016). DOI:https://dx.doi.org/10.1093/nar/gkw914.1362-4962https://scholarworks.montana.edu/handle/1/12611The Escherichia coli type I-E CRISPR-Cas system Cascade effector is a multisubunit complex that binds CRISPR RNA (crRNA). Through its 32-nucleotide spacer sequence, Cascade-bound crRNA recognizes protospacers in foreign DNA, causing its destruction during CRISPR interference or acquisition of additional spacers in CRISPR array during primed CRISPR adaptation. Within Cascade, the crRNA spacer interacts with a hexamer of Cas7 subunits. We show that crRNAs with a spacer length reduced to 14 nucleotides cause primed adaptation, while crRNAs with spacer lengths of more than 20 nucleotides cause both primed adaptation and target interference in vivo Shortened crRNAs assemble into altered-stoichiometry Cascade effector complexes containing less than the normal amount of Cas7 subunits. The results show that Cascade assembly is driven by crRNA and suggest that multisubunit type I CRISPR effectors may have evolved from much simpler ancestral complexes.en-UShttp://creativecommons.org/licenses/by-nc/4.0/legalcodeArticle