| Literature DB >> 28781234 |
Takashi Yamano1, Bernd Zetsche2, Ryuichiro Ishitani1, Feng Zhang2, Hiroshi Nishimasu3, Osamu Nureki4.
Abstract
The RNA-guided Cpf1 (also known as Cas12a) nuclease associates with a CRISPR RNA (crRNA) and cleaves the double-stranded DNA target complementary to the crRNA guide. The two Cpf1 orthologs from Acidaminococcus sp. (AsCpf1) and Lachnospiraceae bacterium (LbCpf1) have been harnessed for eukaryotic genome editing. Cpf1 requires a specific nucleotide sequence, called a protospacer adjacent motif (PAM), for target recognition. Besides the canonical TTTV PAM, Cpf1 recognizes suboptimal C-containing PAMs. Here, we report four crystal structures of LbCpf1 in complex with the crRNA and its target DNA containing either TTTA, TCTA, TCCA, or CCCA as the PAM. These structures revealed that, depending on the PAM sequences, LbCpf1 undergoes conformational changes to form altered interactions with the PAM-containing DNA duplexes, thereby achieving the relaxed PAM recognition. Collectively, the present structures advance our mechanistic understanding of the PAM-dependent, crRNA-guided DNA cleavage by the Cpf1 family nucleases.Entities:
Keywords: CRISPR-Cas; Cas12a; Cpf1; crystal structure; protospacer adjacent motif
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Year: 2017 PMID: 28781234 PMCID: PMC5957536 DOI: 10.1016/j.molcel.2017.06.035
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970