Structural Basis for the Canonical and Non-canonical PAM Recognition by CRISPR-Cpf1.

Mol Cell
Authors
Keywords
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.

Year of Publication
2017
Journal
Mol Cell
Volume
67
Issue
4
Pages
633-645.e3
Date Published
2017 Aug 17
ISSN
1097-4164
DOI
10.1016/j.molcel.2017.06.035
PubMed ID
28781234
PubMed Central ID
PMC5957536
Links
Grant list
DP1 MH100706 / MH / NIMH NIH HHS / United States
R01 DK097768 / DK / NIDDK NIH HHS / United States
R01 MH110049 / MH / NIMH NIH HHS / United States