Compositions, systems, and methods for genome editing
This disclosure provides compositions, recombinant expression constructs, and engineered systems that include a polynucleotide including or encoding a Cas12a tracrRNA, and methods for their use. The materials and methods of the disclosure are especially suited to sequence-specific genome editing of eukaryotic genomic sequences.
1. A DNA expression system comprising
(a) DNA sequence for a first promoter; and
(b) operably linked and heterologous to the first promoter, a DNA encoding a first RNA molecule comprising a Cas12a tracrRNA and comprising a restriction endonuclease cleavage site that is suitable for insertion of a sequence coding for a functional RNA moiety, wherein the Cas12a tracrRNA comprises a sequence selected from the group consisting of SEQ ID NOs:1, 3, 6, 139-146, and 149-169; and
(c) optionally, a terminator 3′ to and operably linked to the DNA encoding the first RNA molecule.
2. The DNA expression system of claim 1 , further comprising:
(d) optionally, a DNA sequence for a second promoter;
(e) operably linked and heterologous to the first promoter or the second promoter, a DNA encoding a Cas12a crRNA capable of hybridizing with a segment of the first RNA molecule; and
(f) optionally, a terminator 3′ to and operably linked to the DNA encoding the Cas12a crRNA.
3. The DNA expression system of claim 2 , wherein the first promoter and the DNA encoding the first RNA molecule and the DNA encoding the Cas12a crRNA are contained in a single construct.
4. The DNA expression system of claim 2 , comprising the second promoter operably linked to the Cas12a crRNA, wherein the first promoter and the DNA encoding the first RNA molecule are contained in a first construct, and the second promoter and the DNA encoding the Cas12a crRNA are contained in a second construct, and wherein the first construct and the second construct are provided (a) in a single vector, or (b) in separate vectors.
5. The DNA expression system of claim 2 , wherein the DNA encoding the Cas12a crRNA comprises a 3′ extension.
6. The DNA expression system of claim 1 , wherein the Cas12a tracrRNA further comprises a 5′ extension.
7. The DNA expression system of claim 2 , wherein the Cas12a crRNA is capable of complexing with a Cas12a nuclease to form a Cas12a ribonucleoprotein complex.
8. The DNA expression system of claim 7 , wherein the Cas12a nuclease is:
(a) a Cas12a nuclease identified from the genome of a bacterial species selected from the group consisting of Francisella tularensis 1, Prevotella albensis , Lachnospiraceae bacterium MC2017 1, Butyrivibrio proteoclasticus , Peregrinibacteria bacterium GW2011_GWA2_33_10, Parcubacteria bacterium GW2011_GWC2_44_17 , Smithella sp. SCADC, Acidaminococcus sp. BV3L6, Lachnospiraceae bacterium MA2020, Candidatus Methanoplasma termitum, Eubacterium eligens, Moraxella bovoculi 237, Leptospira inadai , Lachnospiraceae bacterium ND2006, Porphyromonas crevioricanis 3, Prevotella disiens and Porphyromonas macacae ; or
(b) a Cas12a nuclease selected from the group consisting of LbCas12a, AsCas12a, FnCas12a, and a deactivated Cas12a nuclease; or
(c) a Cas12a nuclease having at least 80% sequence identity with a sequence selected from the group consisting of SEQ ID NOs:11, 107-114, 116-136, and 172; or
(d) a Cas12a nuclease variant selected from the group consisting of (1) a variant LbCpf1 that differs from a wild-type LbCpf1 sequence (SEQ ID NO:135) in containing at least one point mutation selected from the group consisting of G309P, Y312F, M474I, D523N, Q531K, C930A, D937N, V954F/Q, M975L, A984E, I994L, T1006K, I1014V, V1055N/D, L1065F/Y, Y1180F, V1209G, I1229L, V801 I, Y802I, D850A, E943A, and D1198A; (2) a variant AsCpf1 that differs from a wild-type AsCpf1 sequence (SEQ ID NO:134) in containing at least one point mutation selected from the group consisting of L320P, V980A, Q987N, T1004F/Q, K1035E, T1057K, D1107N, F1117Y, N1291 L, D908A, E993A, and D1263A; and (3) a variant FnCpf1 that differs from a wild-type FnCpf1 sequence (SEQ ID NO:172) in containing at least one point mutation selected from the group consisting of 1339P, L342F, Q588K, F1017Q, K1047E, N1118D, F1128Y, L867I, D917A, E1006A, and D1255A.
9. The DNA expression system of claim 1 , wherein the first promoter has a DNA sequence selected from the group consisting of SEQ ID NOs:16-71.
10. A method of tethering a functional RNA molecule to a Cas12a crRNA, the method comprising hybridizing
(a) a functional RNA molecule comprising a Cas12a tracrRNA and a functional RNA moiety, wherein the Cas12a tracrRNA comprises a sequence selected from the group consisting of SEQ ID NOs:1, 3, 6, 139-146, and 149-169; and
(b) a Cas12a crRNA that is capable of hybridizing with a segment of the functional RNA molecule;
thereby tethering the functional RNA molecule to the Cas12a crRNA.
11. The method of claim 10 , wherein the functional RNA molecule is provided by transcription of a DNA molecule comprising a DNA molecule encoding the Cas12a tracrRNA and a DNA molecule encoding the functional RNA moiety, wherein the DNA molecule encoding the functional RNA moiety is or has been inserted at a restriction endonuclease cleavage site in or adjacent to the DNA molecule encoding the Cas12a tracrRNA.
12. The method of claim 10 , wherein the functional RNA moiety is
at least one RNA selected from the group consisting of:
(a) an RNA sequence for annealing to a donor polynucleotide;
(b) an RNA sequence for annealing to a 3′ extension to the crRNA;
(c) a terminator sequence;
(d) an RNA aptamer;
(e) a ribozyme;
(f) an RNA comprising a detectable label;
(g) an RNA bar-coding sequence; and
(h) an RNA sequence forming at least partially double-stranded RNA.
13. The method of claim 10 , wherein the Cas12a crRNA further comprises a 3′ extension.
14. The method of claim 10 , wherein the Cas12a crRNA is complexed with, or is capable of complexing with, a Cas12a nuclease to form a Cas12a ribonucleoprotein complex containing the functional RNA molecule.
15. The method of claim 14 , wherein the Cas12a nuclease is:
(a) a Cas12a nuclease identified from the genome of a bacterial species selected from the group consisting of Francisella tularensis 1, Prevotella albensis , Lachnospiraceae bacterium MC2017 1, Butyrivibrio proteoclasticus , Peregrinibacteria bacterium GW2011_GWA2_33_10, Parcubacteria bacterium GW2011_GWC2_44_17 , Smithella sp. SCADC, Acidaminococcus sp. BV3L6, Lachnospiraceae bacterium MA2020, Candidatus Methanoplasma termitum, Eubacterium eligens, Moraxella bovoculi 237, Leptospira inadai , Lachnospiraceae bacterium ND2006, Porphyromonas crevioricanis 3, Prevotella disiens and Porphyromonas macacae ; or
(b) a Cas12a nuclease selected from the group consisting of LbCas12a, AsCas12a, FnCas12a, and a deactivated Cas12a nuclease; or
(c) a Cas12a nuclease having at least 80% sequence identity with a sequence selected from the group consisting of SEQ ID NOs:11, 107-114, 116-136, and 172; or
(d) a Cas12a nuclease variant selected from the group consisting of (1) a variant LbCpf1 that differs from a wild-type LbCpf1 sequence (SEQ ID NO:135) in containing at least one point mutation selected from the group consisting of G309P, Y312F, M474I, D523N, Q531K, C930A, D937N, V954F/Q, M975L, A984E, I994L, T1006K, I1014V, V1055N/D, L1065F/Y, Y1180F, V1209G, I1229L, V801 I, Y802I, D850A, E943A, and D1198A; (2) a variant AsCpf1 that differs from a wild-type AsCpf1 sequence (SEQ ID NO:134) in containing at least one point mutation selected from the group consisting of L320P, V980A, Q987N, T1004F/Q, K1035E, T1057K, D1107N, F1117Y, N1291L, D908A, E993A, and D1263A; and (3) a variant FnCpf1 that differs from a wild-type FnCpf1 sequence (SEQ ID NO:172) in containing at least one point mutation selected from the group consisting of I339P, L342F, Q588K, F1017Q, K1047E, N1118D, F1128Y, L867I, D917A, E1006A, and D1255A.