WO2005105989A1

WO2005105989A1 - I-dmoi derivatives with enhanced activity at 37°c and use thereof.

Info

Publication number: WO2005105989A1
Application number: PCT/IB2005/001585
Authority: WO
Inventors: Jean-Charles Epinat; Emmanuel Lacroix
Original assignee: Cellectis
Priority date: 2004-04-30
Filing date: 2005-04-27
Publication date: 2005-11-10
Also published as: CA2564513A1; US8211685B2; EP1743026A1; JP2007535322A; EP1743026B1; EP1591521A1; US20080271166A1

Abstract

I-DmoI derivatives with enhanced cleavage activity at 37°C, said mutant comprising a sequence of a mutant of a I-DmoI endonuclease or a chimeric 5 derivative thereof including at least the first I-DmoI domain, said sequence comprising the substitution of at least : (i) one of the residues in positions 4, 20, 49, 52, 92, 94 and/or 95 of said first I-DmoI domain, and/or (ii) one of the residues in positions 101, 102, and/or 109 of the linker or the beginning of the second domain of I-DmoI, if present. 10 Polynucleotide encoding said derivatives, cell, animal or plant comprising said polynucleotide and use thereof for isolating meganucleases with new DNA target specificity.

Description

Ϊ-Dmo I DERIVATIVES WITH ENHANCED ACTIVITY AT 37°C AND USE THEREOF The present invention relates to 1-Dmol derivatives with enhanced cleavage activity at 37°C compared to I-Dmol which is essentially active at high temperature (> 50°C) and displays little or no activity at 37°C. The invention also relates to a polynucleotide encoding said derivatives, to a cell, an animal or a plant comprising said polynucleotide and to their use for isolating meganucleases with new DNA target specificity. Meganucleases are endonucleases, which recognize large (12-45 bp) DNA target sites. In the wild, meganucleases are essentially represented by homing endonucleases, a family of very rare-cutting endonucleases. It was first characterized by the use (in vivo) of the protein I-Scel (Omega nuclease), originally encoded by a mitochondrial group I intron of the yeast Saccharomyces cerevisiae. Homing endonucleases encoded by introns ORF, independent genes or intervening sequences (inteins) present striking structural and functional properties that distinguish them from "classical" restriction enzymes (generally from bacterial system R/MII). They have recognition sequences that span 12-40 bp of DNA, whereas "classical" restriction enzymes recognize much shorter stretches of DNA, in the 3-8 bp range (up to 12 bp for rare-cutter). Therefore, the homing endonucleases present a very low frequency of cleavage, even in the human genome. Furthermore, general asymmetry of homing endonuclease target sequences contrasts with the characteristic dyad symmetry of most restriction enzyme recognition sites. Several homing endonucleases encoded by introns ORF or inteins have been shown to promote the homing of their respective genetic elements into allelic intronless or inteinless sites. By making a site-specific double-strand break in the intronless or inteinless alleles, these nucleases create recombinogenic ends, which engage in a gene conversion process that duplicates the coding sequence and leads to the insertion of an intron or an intervening sequence at the DNA level. Homing endonucleases fall into 4 separated families on the basis of pretty well conserved amino acids motifs. For review, see Chevalier and Stoddard (Nucleic Acids Research, 2001, 29, 3757-3774). One of them is the dodecapeptide family (dodecamer, DOD, D1-D2, LAGLEDADG, P1-P2). This is the largest family of proteins clustered by their most general conserved sequence motif: one or two copies (vast majority) of a twelve-residue sequence: the dodecapeptide. Homing endonucleases with one dodecapeptide (D) are around 20 kDa in molecular mass and act as homodimers. Those with two copies (DD) range from 25 kDa (230 amino acids) to 50 kDa (HO, 545 amino acids) with 70 to 150 residues between each motif and act as monomer. Cleavage is inside the recognition site, leaving 4 nt staggered cut with 3'OH overhangs. 1-Cez.I, and I-Crel (166 amino acids) illustrate the homing endonucleases with one dodecapeptide motif (mono-dodecapeptide). I-Dmol (194 amino acids, SWISSPROT accession number P21505), I-Scel, Pl-Pful and PI-Scel illustrate homing endonucleases with two dodecapeptide motifs. Structural models using X-ray crystallography have been generated for I-Crel (PDB code lg9y), l-Dmol (PDB code lb24), PI-Sce I, Pl-Pful. Structures of I-Crel and PI-Scel (Moure et al., Nat Struct Biol, 2002, 9: 764-70) bound to their DNA site have also been elucidated leading to a number of predictions about specific protein-DNA contacts. Despite an apparent lack of sequence conservation, structural comparisons indicate that LAGLIDADG proteins, should they cut as dimers (like I- Oel) or single chain proteins (like l-Dmol), adopt a similar active confoπnation. In all structures, the LAGLIDADG motifs are central and form two packed α-helices where a 2-fold (pseudo-) symmetry axis separates two monomers or apparent domains. For example, the LAGLIDADG motif corresponds to residues 13 to 21 in l-Crel, and to positions 12 to 20 and 109 to 117, in l-Dmol. On either side of the LAGLIDADG α- helices, a four β-sheet provides a DNA binding interface that drives the interaction of the protein with the half site of the target DNA sequence. l-Dmol is similar to I-Oel dimers, except that the first domain (residues 1 to 95) and the second domain (residues 105 to 194) are separated by a linker (residues 96 to 104) (Epinat et al., Nucleic Acids Res, 2003, 31: 2952-62). Recently, hybrid homing endonucleases were also developped, by fusing two LAGLIDADG nucleases l-Dmol and l-Crel. DmoCre (Epinat et al, precited and NCBI accession numbers CAE85311 and CAE85312) and E-Drel (Chevalier et al., Mol Cell, 2002, 10: 895-905) are two very similar proteins, consisting of the fusion of one of the two l-Dmol domains to l-Crel. For example, DmoCre consists of the residues 1 to 109 of l-Dmol fused to the residues 13 to 166 of l-Crel. The two hybrid or chimeric endonucleases differ only in the linker region, and are able to cleave novel, hybrid DNA targets, made of two moieties, one from the I- Crel cleavage site, the other from the I-Dmol cleavage site. Endonucleases are requisite enzymes for today's advanced genetic engineering techniques, notably for cloning and analyzing genes. Homing endonucleases are very interesting as rare-cutter endonucleases because they have a very low recognition and cleavage frequency in large genome due to the size of their recognition site. Therefore, the homing endonucleases are used for molecular biology and for genetic engineering. It has been shown that induction of double-stranded DNA cleavage at a specific site in chromosomal DNA induces a cellular repair mechanism, which leads to highly efficient recombination events at that locus (WO 96/14408 ; WO 00/46386 ; US 5,830,729 ; Choulika et al., Mol Cell Biol, 1995. 15, 1968-73; Cohen- Tannoudji et al., Mol Cell Biol, 1998. 18, 1444-8; Donoho et al, Mol Cell Biol, 1998, 18, 4070-8 ; Rouet et al, Mol Cell Biol, 1994, 14, 8096-106). Therefore, the introduction of the double-strand break is accompanied by the introduction of a targeting segment of DNA homologous to the region surrounding the cleavage site, which results in the efficient introduction of the targeting sequences into the locus (either to repair a genetic lesion or to alter the chromosomal DNA in some specific way). Alternatively, the induction of a double- strand break at a site of interest is employed to obtain correction of a genetic lesion via a gene conversion event in which the homologous chromosomal DNA sequences from another copy of the gene provide correct sequences to the (mutated) sequences where the double-strand break was induced. This latter strategy leads to the correction of genetic diseases either in which one copy of a defective gene causes the disease phenotype (such as occurs in the case of dominant mutations) or in which mutations occur in both alleles of the gene, but at different locations (as is the case of compound heterozygous mutations). Unfortunately, this method of genome engineering by induction of homologous recombination by a double-strand break is limited by the introduction of a recognition and cleavage site of a natural meganuclease at the position where the recombination event is desired. Despite the diversity of the homing endonuclease family, it is very unlikely to find a natural cleavage site in a sequence of interest. Thus, a lot of efforts have been devoted recently to develop meganucleases with novel specificities in living cells. However, the identification of novel specificities in living cells requires that the meganuclease activity is detectable at mesophilic temperatures. Thus, such assays can be used to look for derivatives of endonucleases such as I-Scel which is active at 30-37°C, but not with thermophilic endonuclease, displaying no or residual activity at 37°C. Therefore, to develop meganucleases with novel specificities in living cells, there is a need of new meganucleases which display significant activity at 37°C. l-Dmol is encoded by an intron from the hyperthermophile archae Desulfurococcus mobilis, and has been shown to be essentially active at high temperature (>50°C; Dalgaard et al., Proc Natl Acad Sci USA, 1993, 90: 5414-7), although some activity was also reported at lower temperature (Chevalier et al., Mol Cell, 2002, 10: 895-905). DmoCre is active essentially at high temperature (65°C) with little or no activity at 37°C (Epinat et al., precited). The inventors have isolated mutants of l-Dmol and DmoCre with an enhanced activity at 37°C, as determined by assays at 37°C. Such mutants carrying mutations in the first domain, the linker or the beginning of the second domain of I- Dmol can be used as initial scaffold for identifying new meganucleases with novel cleavage sites. Therefore, the invention concerns a polypeptide comprising a sequence of a mutant of a l-Dmol homing endonuclease or a chimeric derivative thereof including at least the first l-Dmol domain, said sequence comprising the substitution of at least : (i) one of the residues in positions 4, 20, 49, 52, 92, 94, and/or 95 of said first l-Dmol domain, and/or (ii) one of the residues in positions 101, 102, and/or 109 of the linker or the beginning of the second domain of l-Dmol, if present. According to the invention, the first l-Dmol domain corresponds to positions 1 to 95 in l-Dmol amino acid sequence, the l-Dmol linker to positions 96 to 104 and the beginning of the second l-Dmol domain to positions 105 to 109. In the present invention, unless otherwise mentioned, the residue numbers refer to the amino acid numbering of the l-Dmol sequence SWISSPROT number P21505 or the structure PDB code lb24. The polypeptide mutants according to the present invention represent new l-Dmol derivatives which are active at 37°C compared to l-Dmol which is essentially active at high temperature (> 50°C) and displays little or no activity at 37°C. The invention encompasses the polypeptides comprising or consisting essentially of the sequence as defined above. In particular, the invention encompasses : a) mutants of -wild-type- l-Dmol (l-Dmol mutants) consisting of the first l-Dmol domain as defined above and the second l-Dmol domain (positions 105 to 194), separated by the l-Dmol linker, and b) mutants of hybrid or chimeric l-Dmol (hybrid or chimeric-£>mo mutants) consisting of the fusion of the first l-Dmol domain as defined above, to a sequence of a dimeric LAGLIDADG homing endonuclease (l-Crel for example) or to a domain of another monomeric LAGLIDADG homing endonuclease. In addition, the first l-Dmol domain and the sequence or the domain of the other homing endonuclease may be separated by a linker, for example the l-Dmol linker. In addition to the monomeric mutants as defined in a) and b), the invention encompasses also heterodimeric mutants (heterodimeric-Z)røø mutants) wherein one polypeptide is a mutant of the first l-Dmol domain as defined above, and the other polypeptide is a dimeric LAGLIDADG homing endonuclease (I-Oel for example) or a domain of another monomeric LAGLIDADG homing endonuclease. The chimeric-Dmo or the heterodimeric-E>mσ mutants may include the sequence or the domain of a LAGLIDADG homing endonuclease selected from the group consisting of : I-Sce I, I-Chu I, l-Cre I, I-Csm I, Pl-Sce I, PI-Tli I, PI-Mtu I, I-Ceu I, I-Sce II, I-Sce III, HO, Pi-Civ I, Pl-Ctr I, PI-Aae I, PI-Bsu I, PI-Dha I, PI- Dra I, PI-Mav I, PI-Mch I, PI-Mfu I, PI-Mfl I, PI-Mga I, PI-Mgo I, PI-Min I, PI-Mka I, PI-Mle I, PI-Mma I, PI-Msh I, PI-Msm I, PI-Mth I, PI-Mtu I, PI-Mxe PI-Npu I, Pl-Pfu I, PI-Rma I, Pl-Spb I, PI-Ssp I, PI-Fac I, PI-Mja I, Pl-Pho I, Pi-Tag I, PI-Thy I, PI-Tko I, and PI-Tsp I; preferably, I-Sce I, I-Chu I, I-Dmo I, I-Csm I, P I-Sce I, PI- Pfu I, PI-Tli I, PI-Mtu I, and I-Ceu I; more preferably, 7-Cre I, Pl-Sce I, and Pl-Pfu I ; still more preferably I-Cre I. The polypeptide of the invention may include genetic modifications

(insertion, deletion, substitution, truncation) or chemical modifications in its sequence as defined above, which do not alter the cleavage activity of the resulting polypeptide at 37°C. The modifications may be situated within, or at one or both extremities of said polypeptide. Said modifications include with no limitation: - insertion of one or more residues at the NH₂ terminus and/or COOH terminus, for example: a methionine residue is introduced at the NH₂ terminus, a tag (epitope or polyhistidine sequence) is introduced at the NH terminus and/or COOH terminus; said tag is useful for the detection and/or the purification of said polypeptide, and/or - substitution of one or more residues, for example in positions 1, 47, 51, 55, and/or 107 (MIA, L47A, H51A, L55D, I107L) of the first domain, the linker or the beginning of the second domain of l-Dmol. The cleavage activity of the l-Dmol derivative of the invention may be measured by a direct repeat recombination assay (figure 4), at 37°C, in yeast or mammalian cells, using a reporter vector. The reporter vector comprises two truncated, non-functional copies of a reporter gene (LacZ gene) and a cleavage site within the intervening sequence, cloned in a yeast (figure 3) or a mammalian expression vector (figure 8). The cleavage site (figure 1) is either a l-Dmol cleavage site (l-Dmol mutants) or a hybrid DNA target, made of two moieties, one from the cleavage site of the LAGLIDADG homing endonuclease as defined above, the other from the l-Dmol cleavage site (hybrid l-Dmol mutants). Expression of a meganuclease which is active at 37°C induces cleavage and recombination of the reporter vector, resulting in functional reporter gene expression that can be monitored by appropriate assay. According to an advantageous embodiment of said polypeptide: - the asparagine in position 4 is changed to isoleucine (N4I), - the glycine in position 20 is changed to serine or alanine (G20S or

G20A), - the lysine in position 49 is changed to arginine (K49R), - the isoleucine in position 52 is changed to phenylalanine (I52F), - the alanine in position 92 is changed to threonine (A92T), - the methionine in position 94 is changed to lysine (M94K), - the leucine in position 95 is changed to glutamine (L95Q), - the phenylalanine in position 101 (if present) is changed to cysteine (FlOlC), - the asparagine in position 102 (if present) is changed to isoleucine (N 1021), and/or - the phenylalanine in position 109 (if present) is changed to isoleucine (FI 091). According to another advantageous embodiment of said polypeptide, it is a mutant of l-Dmol comprising the substitution of at least one of the residues in positions 49, 52, 92, 95 and/or 101. Preferably, said l-Dmol mutant comprises at least: the substitution of the isoleucine in position 52, preferably to phenylalanine (I52F), and one or two additional substitutions of the residues in positions 49, 92, 95 and/or 101, as defined above. More preferably, it comprises the substitutions selected from the group consisting of: a) K49R, I52F and L95Q, b) I52F and L95Q, or c) I52F, A92T and FIOIC. Preferably, said l-Dmol mutant derives from the sequence SEQ ID

NO: 1, 2 or 3, most preferably from sequence SEQ ID NO: 1. According to another advantageous embodiment of said polypeptide, it is a mutant of a chimeric-£⁾mo endonuclease consisting of the fusion of the first I- Dmol domain, to a sequence of a dimeric LAGLIDADG homing endonuclease or to a domain of another monomeric LAGLIDADG homing endonuclease, said mutant comprising the substitution of at least: (i) one of the residues in positions 4, 20, and/or 94, and/or (ii) one of the residues in positions 102 or 109, if present. Preferably, the first l-Dmol domain is at the NH₂-terminus of the chimeric-Dmo endonuclease; consequently, the sequence or the domain of the other LAGLIDADG homing endonuclease is at the COOH-terminus of said chimeric--9mo endonuclease. Preferably, said chimeric- mo mutant comprises a linker, preferably a l-Dmol linker consisting of at least 6 consecutive residues from the fragment 96 to 104 of I-DmoI. Preferably, said chimeric-Dmo mutant derives from I-Crel (DmoCre), more preferably from a sequence selected from the group consisting of the sequences SEQ ID NO: 5 to 8. Preferably, said chimeric-Dmo mutant comprises the substitutions selected from the group consisting of: a) G20S, b) G20A, c) M94K and N102I, or d) N4I and F 1091. According to another advantageous embodiment of said polypeptide it is a mutant of an heterodimeric-Z⁾mo endonuclease wherein one polypeptide comprises the sequence of the first I-Dmo-I domain, said sequence comprising the substitution of at least one of the residues in positions 4, 20, 49, 52, 92, 94, and/or 95 as defined above, and the other polypeptide comprises a sequence of a dimeric LAGLIDADG homing endonuclease or a domain of another monomeric LAGLIDADG homing endonuclease. Preferably, said dimeric LAGLIDADG homing endonuclease is I- Crel. The invention also concerns a polynucleotide encoding a polypeptide as defined above. The invention also concerns a vector comprising said polynucleotide. The term "vector" refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of preferred vector is an episome, i.e., a nucleic acid capable of extra-chromosomal replication. Preferred vectors are those capable of autonomous replication and/or expression of nucleic acids to which they are linked. Vectors capable of directing the expression of genes to which they are operatively linked are referred to herein as "expression vectors. A vector according to the present invention comprises, but is not limited to, a YAC (yeast artificial chromosome), a BAC (bacterial artificial), a baculo virus vector, a phage, a phagemid, a cosmid, a viral vector, a plasmid, a RNA vector or a linear or circular DNA or RNA molecule which may consist of chromosomal, non chromosomal, semi-synthetic or synthetic DNA. In general, expression vectors of utility in recombinant DNA techniques are often in the form of "plasmids" which refer generally to circular double stranded DNA loops which, in their vector form are not bound to the chromosome. Large numbers of suitable vectors are known to those of skill in the art. Viral vectors include retrovirus, adenovirus, parvovirus (e.g. adenoassociated viruses), coronavirus, negative strand RNA viruses such as ortho- myxovirus (e. g., influenza virus), rhabdovirus (e. g., rabies and vesicular stomatitis virus), paramyxovirus (e. g. measles and Sendai), positive strand RNA viruses such as picomavirus and alphavirus, and double stranded DNA viruses including adenovirus, herpesvirus (e. g., Herpes Simplex virus types 1 and 2, Epstein-Barr virus, cytomega- lovirus), and poxvirus (e. g., vaccinia, fowlpox and canarypox). Other viruses include Norwalk virus, togavirus, flavivirus, reoviruses, papovavirus, hepadnavirus, and hepatitis virus, for example. Vectors can comprise selectable markers, for example: neomycin phosphotransferase, histidinol dehydrogenase, dihydrofolate reductase, hygromycin phosphotransferase, herpes simplex virus thymidine kinase, adenosine deaminase, glutamine synthetase, and hypoxanthine-guanine phosphoribosyl transferase for eukaryotic cell culture ; TRPl for S. cerevisiae; tetracycline, rifampicin or ampicillin resistance in E. coli. Preferably said vectors are expression vectors, wherein a sequence encoding a polypeptide of the invention is placed under control of appropriate transcriptional and translational control elements to permit production or synthesis of said protein. Therefore, said polynucleotide is comprised in an expression cassette. More particularly, the vector comprises a replication origin, a promoter operatively linked to said encoding polynucleotide, a ribosome site, an RNA-splicing site (when genomic DNA is used), a polyadenylation site and a transcription termination site. It also can comprise an enhancer. Selection of the promoter will depend upon the cell in which the polypeptide is expressed. The invention also concerns a prokaryotic or eukaryotic host cell which is modified by a polynucleotide or a vector as defined above, preferably an expression vector. The invention also concerns a non-human transgenic animal or a transgenic plant, characterized in that all or part of their cells are modified by a polynucleotide or a vector as defined above. As used herein, a cell refers to a prokaryotic cell, such as a bacterial cell, or eukaryotic cell, such as an animal, plant or yeast cell. The polynucleotide sequence encoding the polypeptide of the invention may be prepared by any method known by the man skilled in the art. For example, it is amplified from a cDNA template, by polymerase chain reaction with specific primers. Preferably the codons of said cDNA are chosen to favour the expression of said protein in the desired expression system. The recombinant vectors comprising said polynucleotide may be obtained and introduced in a host cell by the well-known recombinant DNA and genetic engineering techniques. The polypeptide of the invention may be obtained by culturing the host cell containing an expression vector comprising a polynucleotide sequence encoding said polypeptide, under conditions suitable for the expression of the polypeptide, and recovering the polypeptide from the host cell culture. The invention also concerns the use of a polypeptide, a polynucleotide, a vector, a cell, an animal or a plant as defined above for the selection and/or the screening of meganucleases with novel DNA target specificity. For example, the polynucleotide according to the invention may be mutagenized and the resulting mutants may be cloned in an appropriate expression vector and selected and/or screened for their ability to cleave a novel DNA target. The cleavage activity of the resulting mutants may be measured by any appropriate mean. For example, it is measured by a direct repeat recombination assay, at 37°C, in yeast or mammalian cells, using a reporter vector. The reporter vector comprises two truncated, non-functional copies of a reporter gene (LacZ gene) and a novel cleavage site within the intervening sequence, cloned in a yeast or a mammalian expression plasmid. Expression of a meganuclease able to cleave the novel DNA target induces cleavage and recombination of the reporter plasmid, resulting in functional reporter gene expression that can be monitored by an appropriate assay. The present invention will be further illustrated by the additional description and drawings which follows, which refers to examples illustrating the I-

Dmo I derivatives according to the invention. It should be understood however that these examples are given only by way of illustration of the invention and do not constitute in anyway a limitation thereof. - figure 1 represents l-Crel, l-Dmol, and hybrid C1D2 and C2D2 DNA target cut sites (SEQ ID NO: 10- 13), - figure 2 represents the map of the yeast expression vector pCLS0542, used for the screening of the I-Crel and DmoCre mutants, - figure 3 represents the map of the yeast reporter plasmid denominated pCLS0050 ; it contains CUT8, e.g. an I-Oel and an l-Dmol cleavage site as well as an URA3 selectable marker between two direct repeats internal the LacZ gene, - figure 4 represents the principle of the recombination assay to detect meganuclease-induced recombination in yeast or mammal cells. Recombination occurs mostly by Single-Strand-Annealing (SSA). prom: promoter, ter: terminator, - figure 5 represents the characterization of mutants obtained by random mutagenesis of l-Dmol sequence (SEQ ID NO: l). l-Dmol and a set of l-Dmol mutants are tested against an l-Dmol target at 37°C as described in example 1. DmoCre and pCL0S542 (empty vector) are also tested against an l-Dmol target whereas I-Scel is tested against a target with an I-Scel cleavage site. A-V: l-Dmol mutants A: K26N, Δ95; B: N4K, I52F, I60V; C: I52F, L95Q ; D, I, J, M, P: wt (= I- Dmol); E: I19F, I52F, L55Q, F101C; F: Y13C, T76N G, H, O: I52F; K, U: K49R, I52F, L95Q; L: non determined; N: M94L, L95Q; Q, R: I52F, F101C S, T: D7V, I52F; V: I52F, A92T, F101C; 1: I-Scel; 2: pCLS0542; 3: l-Dmol wild type, 4: DmoCre, - figure 6 illustrates an example of l-Dmol mutant. The amino acid sequence of the Dl mutant ( 49R, I52F, L95Q; SEQ ID NO: 4) is aligned with that of the initial l-Dmol sequence (SEQ ID NO: 1) used to generate the mutants. l-Dmol 1B24 (SEQ ID NO:2): sequence corresponding to the structure code lb24 in the PDB protein structure data base. l-Dmol P21505 (SEQ ID NO:3): sequence corresponding to the number P21505 in the SWISSPROT sequence data base. Residue number for I- Dmol mutants refers to the amino acid numbering of the sequence SWISSPROT P21505 or the structure code PDB lb24. For example, K49R mutation corresponds to the mutation of the residue in position 50 of SEQ ID NO:4. - figure 7 represents the characterization of mutants obtained by directed mutagenesis l-Dmol and a set l-Dmol mutants obtained by directed mutagenesis are tested against an l-Dmol target at 37°C as described in example 1. DmoCre and pCLS0542 (empty vector) are also tested against an l-Dmol target whereas I-Scel is tested against a target with an I-Scel cleavage site. A-V: l-Dmol mutants; A: G20S ; B: K49R ; C: I52F; D: A92T ; E: L95Q ; F: F101C ; G K49R/I52F ; H: K49R/A92T ; I: K49R L95Q ; J: K49R/F101C ; K: I52F/A92T ; L I52F/L95Q ; M: I52F/F101C ; N: A92T/L95Q ; O: A92T/F101C ; P: L95Q/F101C; 1 I-Scel; 2: pCLS0542; 3: l-Dmol wild type; 4: 4: K49R, I52F, L95Q; 5: I52F, A92T, F101C; 6: DmoCre, - figure 8 represents the structure of a reporter plasmid for mammalian cell assay. The pCLS0808 plasmid contains l-Dmol cleavage site between two small direct repeats within the LacZ gene. - figure 9 illustrates an example of DmoCre mutant. The amino acid sequence of the DC G20S mutant (A1V, G20S; SEQ ID NO: 9) is aligned with that of the initial DmoCre sequence (DmoCre vl; SEQ ID NO: 5) used for the generation of the mutants. DmoCre v4 (SEQ ID NO: 6): sequence corresponding to the DmoCre construct described in Epinat et al, precited. Residue number for DmoCre mutants refer to the amino acid numbering of the sequence SWISSPROT P21505 or the structure PDB lb24. For example, A1V mutation corresponds to the mutation of the. residue in position 2 of SEQ ID NO: 9. - figure 10 represents the cleavage profile of a set of mutants in yeast. Here, the CUT8 (l-Dmol+l-Crel cleavage sites), l-Dmol, C1D2 and C2D2 cleavage sites are assayed. In each panel, I-Sce I is also assayed with an I-Sce I cleavage site, for positive control. All the other proteins are assayed with the target indicated on the right of the panel. A: I-Scel; B: empty expression vector; C: l-Dmol; D: K49R, I52F, L95Q l-Dmol mutant (see example 1); E: I52F, A92T, F101C I-Dmol mutant (see example 1); F: DmoCre. 1: G20S ; 2: K49R ; 3: 152F ; 4: A92T ; 5: L95Q ; 6: F101C 7: 49M52F ; 8: K49R A92T ; 9: K49R/L95Q ; 10: K49R/F101C ; 11: 152F/A92T 12: I52F/L95Q ; 13: I52F/F101C ; 14: A92T/L95Q ; 15: A92T/F101C ; 16 L95Q/F101C.

Example 1: Characterization of l-Dmol mutants with an enhanced activity at 37°C. DNA manipulations were performed using classical methods, according to standard procedures as those described in Current Protocols in Molecular Biology (Frederick M. AUSUBEL, 2000, Wiley and son Inc, Library of Congress, USA). 1) Material and methods Plasmids A set of l-Dmol mutants expression plasmids were constructed by random or directed mutagenesis of the l-Dmol coding sequence (SEQ ID NO: 1) and subcloning of the resulting sequences into the yeast expression plasmid pCLS0542

(galactose inducible promoter, LEU2 selectable marker and 2 micron origin of replication, figure 2). A reporter plasmid was constructed according to the strategy described in Epinat et al., precited; pCLS0050 comprises a modified LacZ gene with two direct repeats of 825 base pairs separated by l,3kb containing a URA3 selectable marker and a l-Dmol cleavage site (figure 3).

Yeast assay Yeast of a (FYBL2/7B: a, ura3A851, trpIA63, leu2AI, lys2A202) and alpha (FYC2/6A: alpha, trplA63, leu2Al, his3A200) mating type, transformed respectively with the reporter plasmid and the l-Dmol mutant expression plasmid, were grown overnight in selective medium. Then, 2 μl of a and alpha yeast culture were mixed in a final volume of 25 μl of YPD medium (rich media, glucose source) and incubated over night at 30°C without shaking. 2 μl of the suspension was laid on selective medium, for selection of the diploids, with galactose as a carbon source, for induction of strong meganuclease expression. Plates were incubated 24 hours at 30°C and 48 hours at 37°C, before X-Gal staining. For staining, a classic qualitative X-Gal Agarose Overlay Assay was used. Each plate was covered with 2.5 ml of 1% agarose in 0.1 M Sodium Phosphate buffer, pH 7.0, 0.2% SDS, 12% Dimethyl Formamide (DMF), 14 mM β-mercaptoethanol, 0.4% X-Gal, at 60°. Plates were incubated at 37°C.

2) Results l-Dmol mutants with a putative enhanced cleavage activity were generated and assayed in yeast for their ability to induce the specific recombination of a reporter plasmid containing a SSA (Single Strand Annealing) β-galactosidase target. In diploids, expression of an active meganuclease induces cleavage and recombination of the reporter plasmid resulting in a functional LacZ gene that can be monitored by X-Gal staining (Figure 4). Profile of the different clones is shown in Figure 5. Fifteen clones (B, C, E, G, H, K, L, N, O, Q-V) display a blue coloration, ranging from light (Q-T) to dark (C, K, L) blue. Sequencing of the plasmid transformed into these yeast clones showed that the positives present at least nine different sequences (one sequence could not be recovered), each containing the substitution of one ore more residues in positions 49, 52, 92, 95 and/or 101. Results are summarized in Table I. An example of mutant l-Dmol protein corresponding to the sequence SEQ ID NO: 4, is shown in Figure 6. Table I: l-Dmol mutant and cleavage activity in yeast cells at 37°C

^♦Numeration of the amino acids is according to PDB code lt>24 or SWISSPROT P21505. K49R mutation means amino acid 49 is K in l-Dmol wild-type and R in the mutant. Since mutants displayed often several mutations (example: K49R,

I52F, L95Q), in order to assess the impact of each individual substitution, single mutants were generated. A G20S mutant was also generated. This mutant confers an enhanced activity to the DmoCre protein at 37°C (see example 2), and since l-Dmol and DmoCre share the same NH2-terminal aminoacids (see example 2), this mutation could be expected to result in a similar effect with l-Dmol. Characterization of these mutants is shown in Figure 7 and results are summarized in Table I. Several mutants containing the substitution of at least one of the residues in position 52, 95, 49, 92 and/or 101, were shown to have indeed an enhanced activity in yeast at 37°C. Interestingly, the G20S mutation has no effect on l-Dmol activity at 37°C. The activity of the mutants was also detected at 37°C in an in vitro cleavage assay according to the procedure described in Epinat et al., precited.

Example 2; Characterization of chimeric-Z>i^,«o (DmoCre) mutants with an enhanced activity at 37°C. 1) Material and methods - plasmids The mutant l-Dmol coding sequences were transferred in a vector designed for expression in mammalian cells (pTriex4-hygro, NOVAGENE). A mammalian version of the reporter plasmid was constructed using a strategy similar to that described in Epinat et al., precited (figure 8); the promoter and the termination sequences of the yeast plasmid were replaced by an EFlα promoter and a BGH polyadenylation sequence. - Mammalian cells assays CHO cells were co-transfected by the reporter plasmid and the I- Dmol mutant expression plasmid with Superfect transfection reagent, according to the supplier (Qiagen) protocol. 72 hours after transfection, cells were rinsed twice with PBS1X and incubated in lysis buffer (Tris-HCl lOmM pH7.5, NaCl 150mM, Triton XI 00, 0.1 %, BSA, 0.1 mg/ml, protease inhibitors). Lysate was centrifuged and the supernatant used for protein concentration determination and β-galactosidase liquid assay. Typically, 30 μl of extract were combined with 3 μl Mg 100X buffer (MgCl₂ lOOmM, β-mercaptoethanol 35%), 33μl ONPG 8 mg/ml and 234μl sodium phosphate 0.1M pH7.5. After incubation at 37°C, the reaction was stopped with 500μl of 1M Na₂CO₃ and OD was measured at 415nm. The relative β-galactosidase activity is determined as a function of this OD, normalized by the reaction time, and the total protein quantity. 2) Results DmoCre is a chimeric protein including the NH₂-terminal moiety of l-Dmol fused to an I-Oel domain which cleaves hybrid DNA target with an half I- Crel cleavage site and a half l-Dmol site (C1D2, C2D2, figure 1). DmoCre is essentially active at 65°C, with little or no activity at 37°C (Epinat, Arnould et al. 2003, Nucleic Acids Res 31: 2952-62). DmoCre mutants with a putative enhanced activity at 37°C were generated and assayed in yeast with procedures similar to those described in example 1, except that five different reporter plasmids were used: the plasmid bearing CUT8 (Figure 3), and four similar plasmids that contain a single cleavage site, this site being either an I-Crel site, either an l-Dmol site, either C1D2, either C2D2 (Figure 1). In addition, the DmoCre mutants were also tested in mammalian cells using a mammalian version of both the expression and the reporter plasmid. The DmoCre mutants are summarized in Table II. Table II: DmoCre mutants and cleavage activity in yeast and mammalian cells at 37°C

umerat on o t e am no acids s according tol-Dmol sequence SWISSPROT PDB code lb24. G20S mutation means amino acid 20 is G in DmoCre and S in the mutant One example of DmoCre mutant protein sequence (SEQ ID NO: 9) is displayed on figure 9. The majority of the mutants contain the G20S mutation, which by itself results in the strongest activity, as demonstrated with the dark blue staining obtained with the G20S mutant (figure 10). A similar cleavage profile could be observed in yeast and CHO cells, with the majority of the mutants being able to cut the C1D2 and C2D2 target. However, a few out of them did also cut an I-Oel DNA target, which suggest that these specific mutants could have a relaxed activity. Figure 10 also features mutants obtained by directed mutagenesis, such as I52F, L95Q. Such mutations were observed to result in an enhanced activity in l-Dmol at 37°C. Since DmoCre contains the NH2 -terminal moiety of l-Dmol (up to amino acid 109) it could be expected that a I52F, L95Q (for example) version of DmoCre would also have an enhanced activity at 37°C. This was actually not observed, and none of these mutants had any effect on the activity of DmoCre at 37°C. Those results show that proposing mutations that could improve the activity of an enzyme based on results obtained on another molecule is not trivial even if the two proteins have a lot of common features.

Claims

CLAIMS 1°) A polypeptide, characterized in that it comprises a sequence of a mutant of a l-Dmol endonuclease or a chimeric derivative thereof including at least the first l-Dmol domain, said sequence comprising the substitution of at least : (i) one of the residues in positions 4, 20, 49, 52, 92, 94 and/or 95 of said first l-Dmol domain, and/or (ii) one of the residues in positions 101, 102, and/or 109 of the linker or the beginning of the second domain of l-Dmol, if present. 2°) The polypeptide according to claim 1, characterized in that : the asparagine in position 4 is changed to isoleucine (N4I); the glycine in position 20 is changed to serine or alanine (G20S or G20A); the lysine in position 49 is changed to arginine (K49R); the isoleucine in position 52 is changed to phenylalanine (I52F); the alanine in position 92 is changed to threonine (A92T); the methionine in position 94 is changed to lysine (M94K); the leucine in position 95 is changed to glutamine (L95Q); the phenylalanine in position 101 (if present) is changed cysteine (F101C); the asparagine in position 102 (if present) is changed to isoleucine (N102I), and/or the phenylalanine in position 109 (if present) is changed to isoleucine (F109I). 3°) The polypeptide according to claim 1 or claim 2, characterized in that it is a mutant of l-Dmol comprising the substitution of at least one of the residues in positions 49, 52, 92, 95 and/or 101. 4°) The polypeptide according to claim 3, characterized in that said l-Dmo I mutant comprises at least: the substitution of the isoleucine in position 52, preferably to phenylalanine (I52F), and one or two additional substitutions of the residues in positions 49, 92, 95 and/or 101. 5°) The polypeptide according to claim 4, characterized in that it comprises the substitutions selected from the group consisting of: a) K49R, I52F and L95Q, b) I52F and L95Q or c) I52F, A92T and FIOIC. 6°) The polypeptide according to anyone of claims 3 to 5, characterized in that it derives from the sequence SEQ ID NO: 1, 2 or 3. 7°) The polypeptide according to claim 1 or claim 2, characterized in that it is a mutant of a chimeric-_Dmo endonuclease consisting of the fusion of the first l-Dmo I domain to a sequence of a dimeric LAGLIDADG homing endonuclease or to a domain of another monomeric LAGLIDADG homing endonuclease, said mutant comprising the substitution of at least: (i) one of the residues in positions 4 or 20 and/or 94, and/or (ii) one of the residues in positions 102 or 109, if present. 8°) The polypeptide according to claim 7, characterized in that the first l-Dmol domain is at the NH₂-terminus of said chimeric-Dmo endonuclease. 9°) The polypeptide according to claim 7 or 8, characterized in that it comprises a linker, preferably a l-Dmol linker consisting of at least 6 consecutive residues from the fragment 96 to 104 of l-Dmol. 10°) The polypeptide according to anyone of claims 7 to 9, characterized in that it comprises the substitutions selected from the group consisting of: a) G20S, b) G20A, c) M94K and N102I, or d) N4I and F109I. 11°) The polypeptide according to anyone of claims 7 to 10, characterized in that said dimeric LAGLIDADG homing endonuclease is l-Crel. 12°) The polypeptide according to anyone of claims 11, characterized in that it derives from the sequence SEQ ID NO: 5 to 8. 13°) The polypeptide according to claim 1 or claim 2, characterized in that it is a mutant of an heterodimeric--Dmo endonuclease wherein one polypeptide comprises the sequence of the first l-Dmol domain, said sequence comprising the substitution of at least one of the residues in positions 4, 20, 49, 52, 92, 94, and/or 95, and the other polypeptide comprises a sequence of a dimeric LAGLIDADG homing endonuclease or a domain of another monomeric LAGLIDADG homing endonuclease. 14°) The polypeptide according to claim 13, characterized in that said dimeric LAGLIDADG homing endonuclease is l-Crel 15°) The polypeptide according to anyone of claims 1 to 14, characterized in that it comprises a tag at its NH₂ and/or COOH terminus 16°) A polynucleotide, characterized it is encoding the polypeptide according to anyone of claims 1 to 15. 17°) A vector, characterized in that it comprises the polynucleotide according to claim 16. 18°) A host cell, characterized in that it is modified by the polynucleotide according to claim 16 or the vector according to claim 17. 19°) A non-human transgenic animal, characterized in that all or part of its cells are modified by the polynucleotide according to claim 16 or the vector according to claim 17. 20°) A transgenic plant, characterized in that all or part of its cells are modified by the polynucleotide according to claim 16 or the vector according to claim 17. 21°) Use of a polypeptide according to anyone of claims 1 to 15, a polynucleotide according to claim 16, a vector according to claim 17, a cell according to claim 18, an animal according to claim 19 or a plant according to claim 20, for the selection and/or the screening of meganucleases with novel DNA target specificity.