Nucleic acid constructs containing orthogonal site selective recombinases (OSSRs)

Abstract

The present invention provides for a recombinant nucleic acid comprising a nucleotide sequence comprising a plurality of constructs, wherein each construct independently comprises a nucleotide sequence of interest flanked by a pair of recombinase recognition sequences. Each pair of recombinase recognition sequences is recognized by a distinct recombinase. Optionally, each construct can, independently, further comprise one or more genes encoding a recombinase capable of recognizing the pair of recombinase recognition sequences of the construct. The recombinase can be an orthogonal (non-cross reacting), site-selective recombinase (OSSR).

Description

FIELD OF THE INVENTION

This invention relates generally to the use of recombinases.

BACKGROUND OF THE INVENTION

Phage recombinases are splicing enzymes used by virions to insert or remove their genomic DNA from a host chromosome. The use of recombinases (or integrases) for genomic manipulation is well established. Site-specific recombinases are significant tools in a variety of applications in research, medicine, and biotechnology. Conditional gene targeting using site-specific recombinases has enabled the functional analysis of genes, which cannot be inactivated in the germline. Site-specific recombinases also allow the precise integration of open reading frames (ORFs) encoding proteins of interest into highly active gene loci in cell lines and transgenic animals. Recombinases are disclosed in the following references: Groth, Amy C.; Calos, Michele P. J. Mol. Biol (2004) 335, 667-678; Silver, Daniel P.; Livingston, David M. Molecular Cell (2001), 8, 233-243; Sauer, Brian; McDermott, Jeffrey. Nucleic Acids Research (2004) 32(20), 6086-6095; Yagil, Ezra; Dorgai, László; Weisberg, Robert A. J. Mol. Biol (1995) 252, 163-177; and, Dorgai, László; Yagil, Ezra; Weisberg, Robert A. J. Mol. Biol (1995) 252, 178-188.

SUMMARY OF THE INVENTION

The present invention provides for a recombinant nucleic acid comprising a nucleotide sequence comprising a plurality of constructs, wherein each construct independently comprises a nucleotide sequence of interest flanked by a pair of recombinase recognition sequences. Each pair of recombinase recognition sequences is recognized by a distinct recombinase. Optionally, each construct can, independently, further comprise one or more genes encoding a recombinase capable of recognizing the pair of recombinase recognition sequences of the construct.

The present invention provides for a recombinant nucleic acid comprising a first construct and a second construct; wherein the first construct comprises a nucleotide sequence encoding a first recognition sequence of a first recombinase, a second recognition sequence of the first recombinase, and a first nucleotide sequence of interest located between the first and second recognition sequence of the first recombinase; wherein the second construct comprises a nucleotide sequence encoding a first recognition sequence of a second recombinase, a second recognition sequence of the second recombinase, and a second nucleotide sequence of interest located between the first and second recognition sequence of the second recombinase; wherein the second construct is located downstream of the first construct; wherein the first recombinase and the second recombinase do not cross react with the recognition sequence of the other.

A recombinase that can be used in the present invention is an orthogonal (non-cross reacting), site-selective recombinase (OSSR). An OSSR is a recombinase that recognizes a specific recognition site or nucleotide sequence and does not cross-react with the recognition site or nucleotide sequence of another recombinase.

The present invention also provides for a recombinant vector comprising the recombinant nucleic acid. The present invention also provides for a vector or expression vector comprising a recombinant nucleic acid of the present invention.

The present invention further provides for a host cell comprising any of the recombinant nucleic acid or vector of the present invention. In some embodiments, the recombinant nucleic acid is integrated into a chromosome or replicon of the host cell. The host cell can be an eukaryotic or a prokaryotic cell.

The present invention further provides for a host organism comprising one or more host cells of the present invention. In some embodiments, all of the cells of the host organism comprise a recombinant nucleic acid of the present invention.

The present invention provides for a method of excising or deleting one or more nucleotide sequence of interest from a host cell, comprising: (a) providing a signal to a host cell to activate expression from a promoter in the host cell, wherein the host cell comprises a promoter upstream of a plurality of constructs, wherein each construct independently comprises a nucleotide sequence of interest flanked by a pair of recombinase recognition sequences; and (b) excising or deleting one or more nucleotide sequence of interest.

The present invention provides for a method of excising or deleting a first nucleotide sequence of interest from a host cell, comprising: (a) providing a signal to a host cell to activate expression from a promoter in the host cell, wherein the host cell comprises a promoter upstream of a first construct and a second construct; and (b) excising or deleting a first nucleotide sequence of interest; wherein the first construct comprises a nucleotide sequence encoding a first recognition sequence of a first recombinase, a second recognition sequence of the first recombinase, and the first nucleotide sequence of interest located between the first and second recognition sequence of the first recombinase; wherein the second construct comprises a nucleotide sequence encoding a first recognition sequence of a second recombinase, a second recognition sequence of the second recombinase, and a second nucleotide sequence of interest located between the first and second recognition sequence of the second recombinase; wherein the second construct is located downstream of the first construct; wherein the first recombinase and the second recombinase do not cross react with the recognition sequence of the other.

The present invention further provides for a system capable of noise canceling with non-coding interfering RNA suppression.

The present invention further provides for a system capable of noise canceling with dominant negative complexation.

The present invention further provides for a system comprising a switch that is controlled by the relative expression of two variable promoters

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing aspects and others will be readily appreciated by the skilled artisan from the following description of illustrative embodiments when read in conjunction with the accompanying drawings.

FIG. 1 shows an illustration of an exemplary recombinant nucleic acid of the present invention. Three representative constructs are shown. Each horizontal bar represents a separate ORF of interest. Each vertical bar represents a recombinase gene and the triangles with the same hatch marks indicate its corresponding recognition sites. In all figures, each “T” represents a transcription terminator element. In all figures, each L-shaped line with an arrow represents a promoter.

FIG. 2 shows an exemplary Potter Standard Plasmid. The name of such a plasmid is the form of “Vector-Part”. For example, a “Part” is defined as the sequence between BglII and BamHI sites. For example, a “Vector” is defined as the sequence between BamHI and BglII sites. As such, the “Vector” can be defined as a special part containing EcoRI and XhoI restriction sites. Any number of “Parts” and “Vectors” can be individually defined as basic parts or composite parts.

FIG. 3 shows an exemplary standard assembly. The nucleotide sequences from top to bottom are SEQ ID NOs:4-7, respectively.

FIG. 4 shows an exemplary Type I coding sequences, wherein the start and stop codons are placed directly adjacent to the BglII and BamHI sites, respectively. The start codons can be ATG, CTG, TTG, or GTG. The top nucleotide sequence is SEQ ID NO:8, and the bottom nucleotide sequence is SEQ ID NO:9.

FIG. 5 shows exemplary Type II-Type IV coding sequences (SEQ ID NOs:10-12, respectively). The coding sequences allow the construction of ORF fusions for chimeric and tagged proteins. GlySer scars separate junctions between fused peptides.

FIG. 6 shows an exemplary Ribosome Binding Site (RBS), and the spacing of a ribosome binding site relative to the start codon is fixed. Shown is a (likely) strong RBS. The nucleotide sequences from top to bottom are SEQ ID NOs:13-15, respectively.

FIG. 7 shows an exemplary promoter (SEQ ID NO:16). The transcriptional start site (+1) is located at the position directly 5′ to the BamHI site (whenever possible).

FIG. 8 shows an exemplary terminator. The transcriptional termination site is located at the position directly 5′ to the BamHI site (whenever possible). The top nucleotide sequence is SEQ ID NO:17, and the bottom nucleotide sequence is SEQ ID NO:18.

FIG. 9 shows an example of cross pairing (of three different recombinases) which should not result in excision.

FIG. 10 shows a screen based on excision events. In this example, reactive pairs are identified by replica plating from ampicillin (Amp)/chloramphenicol (Cm) plates to kanamycin (Kan)/Cm plates.

FIG. 11 shows a representative testing of cross pairs and simultaneous expression. A large number of constructs is required (ΣN for N recognition sites +2 per recombinase using a three plasmid system) and extensive cross testing.

FIG. 12 shows a representative fusebox expression cassette.

FIG. 13 shows a representative synthetic teleomere.

FIG. 14 shows a system capable of noise canceling with non-coding interfering RNA suppression.

FIG. 15 shows a system capable of noise canceling with dominant negative complexation.

FIG. 16 shows a system comprising a switch that is controlled by the relative expression of two variable promoters

FIG. 17 shows a sample gel showing a cross-test involving Cre, Dre, Cre-Dre and the various site combinations giving the expected results quite cleanly by colony PCR analysis

FIG. 18 shows an “or” gate of the present invention.

FIG. 19 shows the expected results for a circuit in an agar-plate based assay.

FIG. 20 shows the result of a cross testing method using an active site knockout of Dre (DreX-Y324F). Tyrosine Y324 is annotated as the active site tyrosine for this enzyme. However, after replacing this residue with phenylalanine, as determined in the sequencing result shown, activity of the enzyme is still observed. The nucleotide sequences depicted for “p15a-cm-ptet (RK) DreX” and “DreX Second Read” are SEQ ID NO:19. The nucleotide sequence depicted for “p15a-cm-ptet (RK) Dre” is SEQ ID NO:20.

FIG. 21 shows a flowchart for a plate based assay for searching for and using orthogonal site selective recombinases.

DETAILED DESCRIPTION

Before the present invention is described, it is to be understood that this invention is not limited to particular embodiments described, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims.

Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limits of that range is also specifically disclosed. Each smaller range between any stated value or intervening value in a stated range and any other stated or intervening value in that stated range is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included or excluded in the range, and each range where either, neither or both limits are included in the smaller ranges is also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the invention.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned herein are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited.

It must be noted that as used herein and in the appended claims, the singular forms “a”, “and”, and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a sequence” includes a plurality of such sequences, and so forth.

These and other objects, advantages, and features of the invention will become apparent to those persons skilled in the art upon reading the details of the invention as more fully described below.

In some embodiments, the recombinant nucleic acid comprises two or more constructs, three or more constructs, four or more constructs, five or more constructs, or ten or more constructs. In some embodiments, the recombinant nucleic acid comprises up to ten constructs.

In some embodiments, the recombinant nucleic acid further comprises a third construct comprising a nucleotide sequence encoding a first recognition sequence of a third recombinase, a second recognition sequence of the third recombinase, and a third nucleotide sequence of interest located between the first and second recognition sequence of the third recombinase. In some embodiment, the recombinant nucleic acid further comprises a fourth, fifth, or/and etc. construct(s), each construct comprising a nucleotide sequence encoding a first recognition sequence of a unique recombinase, a second recognition sequence of the unique recombinase, and a nucleotide sequence of interest located between the first and second recognition sequence of the unique recombinase, wherein the unique recombinase is a recombinase is distinct of any of the other recombinase which recognizes a recognition sequence within the recombinant nucleic acid.

See FIG. 1 for one embodiment of the invention.

The use of recombinases for manipulation of genomic sequences is well known to those skilled in the art. Commonly, the recombinase is used as follows: a target DNA containing a selection marker is initially inserted into a chromosome at a desired location. Following selection, an OSSR is used to extract the selection marker. In this method, the toolkit of two recombinases and one selection marker can be used repeatedly to significantly modify the organism under study. The orthogonality of the recombinase is important to prevent destructive or unpredictable recombination events.

A recombinase that can be used in the present invention is an orthogonal (non-cross reacting), site-selective recombinase (OSSR). An OSSR is a recombinase that recognizes a specific recognition site or nucleotide sequence and does not cross-react with the recognition site or nucleotide sequence of another recombinase. In some embodiments, each recombinase recognizes a pair of identical DNA sequences is that is about 50 to 60 basepair in length. In some embodiments, the recombinase recognizes a pair of identical DNA sequences is that is about 52 to 58 basepair in length. In some embodiments, the recombinase recognizes a pair of identical DNA sequences is that is about 53, 54, 55, 56 or 57 basepair in length. If only two sites are present, and they are oriented in the same direction on a DNA strand, the sequence between the sites is excised into a loop, with one recognition site remaining on the annealed DNA and one site incorporated into the loop. If more than two sites are present, or the orientation between sites is different, multiple activities can occur, including flipping and mis-annealing of the genomic DNA.

To be useful for the present invention, the recombinase and its recognition sites must display the following properties: (1) Engineered recognition sites should be unique to the cell (that is, no native genomic sequence matches the recognition site). (2) Recombinases must not bind to the recognition sites associated with other recombinases. (3) Recombinases bound to a recognition site must not be able to bind to the “partner” recombinase associated with a different recognition site. (The functional unit of a recombinase is a dimer of dimers. For example, dimer AA normally binds to site a. This then interacts with another dimer AA bound to a different site a to cause a recombination event. If dimer AA recognizes site a, and dimer BB recognizes site b, if AA is capable of binding to BB in the presence of a and b, a cross reaction would occur.) (4) Recognition sites should be kept to a total of two per cell per recombinase in all cases where this is possible during the operation of the invention. FIG. 9 shows an example of cross pairing (of three different recombinases) which should not result in excision. FIG. 10 shows a screen based on excision events. FIG. 11 shows a representative testing of cross pairs and simultaneous expression.

Recombinases useful for this invention include, but are not limited to, to the recombinases listed in Table 1.

TABLE 1
Recombinases.
#	Name	Host	Organism	Gene	Accession
1	BSu_xerC	Bacillus subtilis	chromosome	codV	P39776
2	BSu_xerD	Bacillus subtilis	chromosome	ripX	P46352
3	BSu_ydcL	Bacillus subtilis	chromosome	ydcL	A69774
4	CBu_tnpA	Clostridium butyricum	chromosome	tnpA	S40097
5	Col1D	Escherichia coli	plasmid F	D	P06615
6	CP4-57	Escherichia coli	chromosome	Int	P32053
7	Cre	Escherichia coli	phage P1	Int	P06956
8	D29	Mycobacterium smegmatis	phage D29	Int	AAC18476
9	DLP12	Escherichia coli	phage DLP12	Int	P24218
10	DNo_int	Dichelobacter nodosus	chromosome	Orf	AAB00935
11	ECo_fimB	Escherichia coli	chromosome	fimB	P04742
12	ECo_fimE	Escherichia coli	chromosome	fimE	P04741
13	ECo_orf	Escherichia coli	chromosome	b2442	A65019
14	ECo_xerC	Escherichia coli	chromosome	xerC	C37841
15	ECo_xerD	Escherichia coli	chromosome	xerD	P21891
16	HIn_orf	Haemophilus influenzae	chromosome	orf1572	P46495
17	HIn_rci	Haemophilus influenzae	chromosome	rci	P45198
18	HIn_xerC	Haemophilus influenzae	chromosome	xerC	P44818
19	HIn_xerD	Haemophilus influenzae	chromosome	xerD	P44630
20	HK22	Escherichia coli	phage HK022	int	AAF30377
21	HP1	Haemophilus influenzae	phage HP1	int	P21442
22	L2	Acholeplasma sp.	phage L2	int	AAA87961
23	L5	Mycobacterium tuberculosis	phage L5	int	CAA79409
24	L54	Staphylococcus aureus	phage L54	int	P20709
25	Lambda	Escherichia coli	phage lambda	int	AAA96562
26	LLe_orf	Lactobacillus leichmannii	chromosome	orf	CAA55635
27	LLe_xerC	Lactobacillus leichmannii	chromosome	xerC	CAA59018
28	phi10MC	Oenococcus oeni	phage phi10MC	int	AAD00268
29	MJa_orf	Methanococcus jannaschi	chromosome	orf	Q57813
30	MLe_xerD	Mycobacterium leprae	chromosome	xerD	S72959
31	MPa_int	Mycobacterium paratuberculosis	chromosome	int	AAA88834
32	MTu_int	Mycobacterium tuberculosis	chromosome	int	B70965
33	MTu_xerC	Mycobacterium tuberculosis	chromosome	xerC	Q10815
34	MV4	Lactobacillus delbrueckii	phage MV4	int	AAC48859
35	MX8	Myxococcus xanthus	phage Mx8	int	AAC48895
36	pAE1	Alcaligenes eutrophus	plasmid pAE1	orf	AAA87238
37	pCL1	Chlorobium limicola	plasmid pCL1	fim	AAB36935
38	pDU1	Nostoc sp.	plasmid pDU1	orf	AAA17517
			plasmid
39	pMEA	Amycolatopsis methanolica	pMEA300	orf	AAB00469
			plasmid
40	RSp_EF	Rhizobium sp.	pNG234a	EF	P55429
			plasmid
41	RSp_GC	Rhizobium sp.	pNG234a	GC	P55459
			plasmid
42	RSp_QK	Rhizobium sp.	pNG234a	QK	P55632
			plasmid
43	RSp_RA	Rhizobium sp.	pNG234a	RA	AAB92467
			plasmid
44	RSp_RB	Rhizobium sp.	pNG234a	RB	P55635
			plasmid
45	RSp_RC	Rhizobium sp.	pNG234a	RC	P55636
			plasmid
46	RSp_RD	Rhizobium sp.	pNG234a	RD	P55637
			plasmid
47	RSp_RE	Rhizobium sp.	pNG234a	RE	P55638
			plasmid
48	RSp_RF	Rhizobium sp.	pNG234a	RF	P55639
49	pSAM2	Streptomyces ambofaciens	plasmid pSAM2	orf	P15435
50	pSDL2	Salmonella dublin	plasmid pSDL2	resV	A38114
51	pSE101	Saccharopolyspora erythraea	plasmid pSE101	orf	S41725
52	pSE211	Saccharopolyspora erythraea	plasmid pSE211	orf	P22877
53	pWS58	Lactobacillus delbrueckii	plasmid pWS58	orf	CAA90472
54	phi-11	Staphylococcus aureus	phage phi11	int	AAA32198
55	phi-13	Staphylococcus aureus	phage phi13	int	S52761
56	phi-80	Escherichia coli phage	phage phi80	int	CAA27683
57	phi-adh	Lactobacillus gasseri	phage phi-adh	int	JN0535
58	phi-CTX	Pseudomonas aeruginosa	phage phiCTX	int	CAA74224
59	phi-g1e	Lactobacillus sp.	phage phi-g1e	int	T13182
60	phi-LC3	Lactococcus lactis	phage phiLC3	int	A47085
61	phi-R73	Escherichia coli	phage phi-R73	int	A42465
62	P186	Escherichia coli	phage 186	int	AAC34175
63	P2	Escherichia coli	phage P2	int	AAD03297
64	P21	Escherichia coli	phage P21	int	AAC48886
65	P22	Salmonella typhimurium	phage P22	int	AAF75002
66	P4	Escherichia coli	phage P4	int	CAA29379
67	P434	Escherichia coli	phage 434	int	P27078
68	PAe_xerC	Pseudomonas aeruginosa	chromosome	sss	AAG08665
69	PMi_fimB	Proteus mirabilis	chromosome	fimB	CAB61438
			plasmid IncI2
70	R721	Escherichia coli	(R721)	rcb	G45252
			plasmid IncI1
71	Rci	Escherichia coli	(R64)	rci	P10487
72	SF6	Shigella flexneri	phage Sf6	int	P37317
73	SLP1	Streptomyces coelicolor	plasmid SLP1	orf	CAC08268
74	IntI3	Serratia marcescens	chromosome	orf	BAA08929
75	SsrA	Methanosarcina acetivorans	plasmid pC2A	ssrA	AAB39744
76	SSV1	Sulfolobus sp.	phage SSV1	int	CAA30211
77	T12	Streptococcus pyogenes	phage T12	int	AAC488867
78	IntI1	Escherichia coli	transposon Tn21	int	AAA82254
			transposon
79	Tn4430	Bacillus thuringiensis	Tn4430	int	CAA30491
			transposon
80	Tn5041	Pseudomonas sp.	Tn5041	orfI	CAA67462
			transposon
81	Tn5252	Streptococcus pneumoniae	Tn5252	int	A55863
			transposon
82	Tn5276	Lactobacillus lactis	Tn5276	int	C55205
			transposon
83	Tn554a	Staphylococcus aureus	Tn554	tnpA	P06696
			transposon
84	Tn554b	Staphylococcus aureus	Tn554	tnpB	P06697
85	IntI2	Escherichia coli	transposon Tn7	int	CAA05031
			transposon
86	Tn916	Entercoccus faecalis	Tn916	int	P22886
87	Tuc	Lactobacillus lactis	phage Tuc2009	int	AAA32608
88	BZo_int	Bergeyella zoohelcum	chromosome	orf	AAA50502
89	ASp_xisA	Anabaena sp.	chromosome	xisA	P08862
90	ASp_xisC	Anabaena sp.	chromosome	xisC	Q44217
91	FLP	Saccharomyces cerevisiae	plasmid 2μ	FLP	J01347
92	pKD1	Kluyveromyces lactis	plasmid pKD1	FLP	P13783
93	pSB2	Zygosaccharomyces bailii	plasmid pSB2	FLP	M18274
94	pSB3	Zygosaccharomyces bisporus	plasmid pSB3	FLP	P13784
95	pSM1	Zygosaccharomyces fermentati	plasmid pSM1	FLP	P13770
96	pSR1	Zygosaccharomyces rouxii	plasmid pSR1	FLP	P13785
97	HPy_xerC	Helicobacter pylori	chromosome	xerC	C64604
98	HPy_xerD	Helicobacter pylori	chromosome	xerD	C64644
99	Eco_Rac	Escherichia coli	chromosome	int	P76056
100	Eco_Qin	Escherichia coli	chromosome	int	P76168
101	CP4-6	Escherichia coli	chromosome	orf	P71928
102	E14	Escherichia coli	chromosome	int	P75969
103	MGo_orf	Mycobacterium gordonae	chromosome	orf	AAB54012
104	MLe_xerC	Mycobacterium leprae	chromosome	xerC	CAB10656
105	MTu_xerD	Mycobacterium tuberculosis	chromosome	xerD	CAB10958
106	pEAF	Escherichia coli	plasmid EAF	rsv	AAC44039
107	PF1_xerC	Pseudomonas fluorescens	chromosome	sss	T10461
108	PWi_orf	Protothera wickerhamii	mitochondria	ymf42	T11912
109	Sfi21	Streptococcus thermophilus	phage Sfi21	int	AAD44095
110	phi-r1t	Lactobacillus lactis	phage r1t	int	AAB18676
111	STy_xerC	Salmonella typhimurium	chromosome	xerC	P55888
112	STy_xerD	Salmonella typhimurium	chromosome	xerD	P55889
113	SSp_orf	Synechocystis sp.	chromosome	orf	BAA16682
114	DNo_orf	Dichelobacter nodosus	chromosome	orf	AAB00935
115	VCh_orf	Vibrio cholerae	chromosome	orf	AAC44230
		Methanothermobacter
116	MMa_xerC	marburgensis	chromosome	xerC	D69219
117	ECo_orf2	Escherichia coli	chromosome	intB	P39347
118	SIn_orf	Salmonella infantis	chromosome	orf	J03391
119	BK-T	Lactococcus lactis	phage BK-T	int	T13262
120	phi-42	Staphylococcus aureus	phage phi42	int	AAA91615
121	FRAT1	Mycobacterium sp.	phage FRAT1	int	P25426
122	HZe_vlf1	Helicoverpa zea	chromosome	vlf1	AAA58702
123	pKW1	Kluveromyces waltii	plasmid pKW1	FLP	X56553
124	CBu_tnpB	Clostridium butyricum	chromosome	tnpB	S40098
125	S2	Haemophilus influenzae	phage S2	int	CAA96221
126	NBU1	Bacteroides uniformis	plasmid NBU1	int	AAF74437
			transposon
127	Tn1545	Streptococcus pneumoniae	Tn1545	int	P27451
128	T270	Streptococcus pyogenes	phage T270	int	AAA85500
129	PMi_xerC	Proteus mirabilis	chromosome	xerC	AAB87500
130	PMi_xerD	Proteus mirabilis	chromosome	xerD	AAB87499
131	phiV	Shigella flexneri	phage V	int	AAB72135
132	O1205	Streptococcus thermophilus	phage O1205	int	T13289
			transposon
133	Tn4556	Streptomyces fradiae	Tn4556	int	P20184
134	MS6	Mycobacterium sp.	phage Ms6	int	AAD03774
			plasmid
135	pFAJ	Rhodococcus erythropolis	pFAJ2600	pmrA	AAC45806
136	SMa_xerC	Serratia marcescens	chromosome	xerC	AAC46276
			plasmid
137	pTiA6	Agrobacterium tumefaciens	pTiA6NC	int	AAB91569
138	AAe_orf	Aquifex aeolicus	chromosome	int	G70397
			transposon
139	Tn557	Staphylococcus aureus	Tn557	int	AAC28969
140	EAe_int	Enterobacter aerogenes	chromosome	int	AAB95339
141	SF2	Shigella flexneri	phage Sf2	int	AAC39270
142	ECo_yfdB	Escherichia coli	chromosome	yfdB	P37326
143	RP3	Streptomyces rimosus	phage RP3	int	X80661
144	VWB	Streptomyces venezuelae	phage VWB	int	CAA03882
145	SEx_vlf1	Spodoptera exigua	chromosome	vlf1	AAF33611
146	STy_rci	Salmonella typhimurium	chromosome	rci	AAC38070
147	PPu_orf	Pseudomonas putida	chromosome	orf	CAA06238
148	A2	Lactobacillus casei	phage A2	int	CAA73344
149	pECE1	Aquifex aeolicus	plasmid ece1	int	AAC07955
150	MLo_int	Mesorhizobium loti	chromosome	intS	AAC24508
151	SRu_orf	Selenomonas ruminantium	chromosome	orf	BAA24921
152	pQPRS	Coxiella burnetti	plasmid pQPRS	int	CAA75853
153	PRe_orf	Panagrellus redivivus	chromosome	orf	CAA43185
154	CEl_orf	Caenorhabditis elegans	chromosome	orf	Z82079
155	IntI4	Vibrio cholerae	chromosome	intI4	AAF71178
156	SMu_orf	Streptococcus mutans NG8	chromosome	orfA	AAC17173
157	phiU	Rhizobium leguminosarum	phage phiU	int	BAA25885
158	PHo_xerC	Pyrococcus horikoshii	chromosome	xerC	B71194
159	RCa_orf1	Rhodobacter capsulatus	chromosome	orf1	T03499
160	RCa_orf2	Rhodobacter capsulatus	chromosome	orf2	T03567
			transposon
161	Tn5382	Enterococcus faecium	Tn5382	int	AAC34799
		Methanothermobacter
162	psiM2	marburgensis	phage PsiM2	int	T12745
163	STy_orf	Salmonella typhimurium	chromosome	orf	T03001
164	MTu_orf	Mycobacterium tuberculosis	chromosome	Rv2659c	G70966
165	TPa_xerC	Treponema pallidum	chromosome	codV	AAC65375
166	TPa_xerD	Treponema pallidum	chromosome	xprB	AAC65379
167	CTr_xerC	Chlamydia trachomatis	chromosome	xerC	AAC67942
168	CTr_xerD	Chlamydia trachomatis	chromosome	xerD	AAC68462
169	phiPVL	Staphylococcus aureus	phage phiPVL	int	BAA31902
170	pNL1	Sphingomonas aromaticivorans	plasmid pNL1	int	AAD03886
171	CP4-157	Escherichia coli O157:H7	chromosome	int	AAC31482
172	SAu_xerD	Staphylococcus aureus	chromosome	xerD	AAC64162
173	YPe_orf	Yersinia pestis	chromosome	orf	AAC69581
174	RPr_xerD	Rickettsia prowazekii	chromosome	xerD	B71693
175	RPr_xerC	Rickettsia prowazekii	chromosome	xerC	B71643
176	VCh_SXT	Vibrio cholerae	chromosome	orf	AAF93686
177	AAc_orf	Actinob. actinomycetemcomitans	chromosome	orf	AAC70901
178	MAV1	Mycoplasma arthritidis	chromosome	int	AAC33780
179	fOg44	Oenococcus oeni	phage fOg44	int	AAD10711
180	SFX	Shigella flexneri	phage SFX	int	AAD10295
			transposon
181	Tn4371	Ralstonia eutropha	Tn4371	int	CAA71790
182	HPy_orf	Helicobacter pylori	chromosome	orf	A71869
183	CPn_xerC	Chlamydia pneumoniae	chromosome	xerD	BAA99231
184	CPn_xerD	Chlamydia pneumoniae	chromosome	xerC	BAA98236
185	K139	Vibrio cholerae	phage K139	int	AAD22068
186	PPu_orf2	Pseudomonas putida	chromosome	orf	BAA75916
			plasmid
187	pPZG	Pantoea citrea	pPZG500	int	AAD21210
188	H19J	Escherichia coli	phage H19J	int	CAB38715
189	phi304L	Corynebacterium glutamicum	phage phi304L	int	CAB38562
190	SCo_orf	Streptomyces coelicolor	chromosome	orf	T36198
191	phi16	Corynebacterium glutamicum	phage phi16	int	CAA73074
192	BHa_xerC	Bacillus halodurans	chromosome	codV	BAB06184
193	XFa_xerC	Xylella fastidiosa	chromosome	xerC	AAF84292
194	BHa_xerD	Bacillus halodurans	chromosome	xerD	BAB05248
195	PAe_xerD	Pseudomonas aeruginosa	chromosome	xerD	AAG07125
196	VCh_xerC	Vibrio cholerae	chromosome	xerC	AAF93305
197	VCh_xerD	Vibrio cholerae	chromosome	xerD	AAF95562
198	NMa_xerC	Neisseria meningitidis ser. A	chromosome	xerC	CAB83879
199	NMb_xerC	Neisseria meningitidis ser. B	chromosome	xerC	AAF42202
200	XFa_xerD	Xylella fastidiosa	chromosome	xerD	AAF84234
201	CMu_xerC	Chlamydia muridarum	chromosome	xerC	AAF73578
202	SAu_xerC	Staphylococcus aureus	chromosome	xerC	AAF89877
203	NMa_xerD	Neisseria meningitidis ser. B	chromosome	xerD	AAF41164
204	NMb_xerD	Neisseria meningitidis ser. A	chromosome	xerD	CAB84234
205	CMu_xerD	Chlamydia muridarum	chromosome	xerD	AAF39124
206	PAb_xerD	Pyrococcus abysii	chromosome	xerD	A75153
207	pI3	Deinococcus radiodurans	plasmid pI3	ResU	AAF44051
			plasmid
208	pTiSAK	Agrobacterium tumefaciens	TiSAKURA	orf36	BAA87661
209	HPj_xerC	Helicobacter pylori J	chromosome	xerC	B71910
210	TMa_xerC	Thermotoga maritima	chromosome	xerC	D72312
211	CJe_xerD	Campylobacter jejuni	chromosome	xerD	CAB73128
212	APe_xerD	Aeropyrum pernix	chromosome	xerD	G72672
213	PSy_orf	Pseudomonas syringae	chromosome	orfF	CAB96970
214	MM1	Streptococcus pneumoniae	phage MM1	int	CAB96616
215	XNi_vlf1	Xestia nigrum	chromosome	vlf1	AAF05239
216	PXy_vlf1	Plutella xylostella	chromosome	vlf1	AAG27387
217	pXO1-132	Bacillus anthracis	plasmid pXO1	132	D59107
			transposon
218	Tn4555	Bacteroides fragilis	Tn4555	int	AAB53787
219	DRa_xer	Deinococcus radiodurans	chromosome	xerD	G75636
220	BJa_int	Bradyrhizobium japonicum	chromosome	intA	AAF64651
221	BHa_orf4	Bacillus halodurans	chromosome	BH2349	BAB06068
222	pXO1-103	Bacillus anthracis	plasmid pXO1	103	G59103
223	PAe_orf2	Pseudomonas aeruginosa	chromosome	orf2	AAG04117
			plasmid
224	pLGV440	Chlamydia trachomatis	pLGV440	orf8	P08788
			transposon
225	Tn5520	Bacteroides fragilis	Tn5520	bipH	AAC80279
226	pNL1_tnpA	Sphingomonas aromaticivorans	plasmid pNL1	tnpA	AAD03922
227	CTr_orf	Chlamydia trachomatis	chromosome	orf1	S44160
228	BHa_orf1	Bacillus halodurans	chromosome	BH3551	BAB07270
229	phi-933W	Escherichia coli	phage 933W	int	AAD25406
230	CPs_orf1	Chlamydia psittaci	chromosome	orf	B39999
231	VCh_orf2	Vibrio cholerae	chromosome	VC1758	AAF94908
232	DRa_orf2	Deinococcus radiodurans	chromosome	orf2	F75611
233	pCPnE1	Chlamydophila pneumoniae	plasmid pCPnE1	orf2	CAA57585
234	ECo_intB	Escherichia coli	chromosome	intB	AAD37509
235	UUr_xerC	Ureaplasma urealyticum	chromosome	xerC	AAF30630
236	HK97	Escherichia coli	phage HK97	int	AAF31094
237	TPW22	Lactococcus sp.	phage TPW22	int	AAF12706
238	APSE-1	Acyrthosiphon pisum	phage APSE-1	int	AAF03981
			plasmid
239	pURB500	Methanococcus maripaludis	pURB500	int	AAC45247
240	SFl_int	Shigella flexneri	chromosome	int	AAD44730
241	UUr_xerD	Ureaplasma urealyticum	chromosome	ripX	AAF30551
242	Wphi	Escherichia coli	phage Wphi	int	CAB54522
243	BHa_orf2	Bacillus halodurans	chromosome	BH2364	BAB06083
244	SEn_int	Salmonella enterica	chromosome	intI5	AAG03003
245	pCP1	Deinococcus radiodurans	plasmid pCP1	xerD	AAF12667
246	SCo_int	Streptomyces coelicolor	chromosome	int	CAB71253
247	PRi1724	Agrobacterium rhizogenes	plasmid pRi1724	orf9	BAB16128
248	SCo_traS	Streptomyces coelicolor	chromosome	traS	T35465
249	HPy_orf1	Helicobacter pylori	chromosome	orf	A71870
250	XFa_orf1	Xylella fastidiosa	chromosome	XF2530	AAF85328
251	UUr_codV	Ureaplasma urealyticum	chromosome	codV	AAF30942
252	pXO1-18	Bacillus anthracis	plasmid pXO1	18	B59093
253	CPs_orf2	Chlamydia psittaci	chromosome	orf2	A39999
254	SPBc2	Bacillus subtilis	phage SPBc2	yopP	T12850
255	D3	Pseudomonas aeruginosa	phage D3	int	AAF04808
256	XFa_orf2	Xylella fastidiosa	chromosome	XF1642	AAF84451
257	XFa_orf3	Xylella fastidiosa	chromosome	XF0678	AAF83488
			plasmid
258	pLGV440-2	Chlamydia trachomatis	pLGV440	N1	S01180
259	pB171	Escherichia coli	plasmid pB171	rsvB	BAA84906
260	DRa_orf3	Deinococcus radiodurans	chromosome	orf	C75509
261	CPZ-55	Escherichia coli	phage CPZ-55	int	P76542
			transposon
262	ICESt1	Streptococcus thermophilus	ICESt1	int	CAB70622
263	pGP7-D	Chlamydia trachomatis	plasmid pGP7-D	TCA01	AAF39715
264	XFa_orf4	Xylella fastidiosa	chromosome	XF1718	AAF84527
265	HIn_orf2	Haemophilus influenzae	chromosome	int	AAF27347
266	DNo_orf2	Dichelobacter nodosus	chromosome	intC	CAB57348
			transposon
267	NBU2	Bacteroides fragilis	NBU2	intN2	AAF74726
			plasmid Col1B-
268	pCol1B	Shigella sonnei	P9	resA	BAA75108
269	PSy_orf4	Pseudomonas syringiae	chromosome	orf	CAC14205
			transposon
270	Tn4652	Pseudomonas putida	Tn4652	orf5	AAD44277
			plasmid
271	pLGV440-3	Chlamydia trachomatis	pLGV440	orf7	P10561
272	pF	Escherichia coli	plasmid F	int	BAA97902
273	BHa_orf3	Bacillus halodurans	chromosome	BH4039	BAB07758
274	XFa_orf5	Xylella fastidiosa	chromosome	XF2132	AAF84931
			plasmid
275	pNRC100_1	Halobacterium sp.	pNRC100	H0618	T08273
276	SDy_orf	Shigella dysenteriae	chromosome	int	AAF28112
277	pQpRS_2	Coxiella burnetti	plasmid pQpRS	orf410	CAA75839
278	PMu_rci	Pasteurella multocida	chromosome	rci	AAF68420
279	SPBc2	Bacillus subtilis	phage SPBc2	yomM	AAC13009
280	PPa_int	Pseudomonas pavonaceae	chromosome	intP	CAB65361
			plasmid
281	pKLC102	Pseudomonas aeruginosa	pKLC102	xerC	AAG02084
282	XFa_orf6	Xylella fastidiosa	chromosome	XF0631	AAF83441
283	SCo_orf3	Streptomyces coelicolor	chromosome	int	CAC14368
284	LLa_orf	Lactococcus lactis	chromosome	orf3	AAF86683
285	MSp_orf	Mycobacterium sp.	chromosome	intM	CAB65286
286	pNL1_tnpB	Sphingomonas aromaticivorans	plasmid pNL1	tnpB	AAD03921
287	XFa_orf7	Xylella fastidiosa	chromosome	XF0968	AAF83778
288	ECo_orf5	Escherichia coli	chromosome	int	AAF06962
289	AGe_vlf1	Anticarsia gemmatalis	chromosome	vlf-1	AAD54607
290	pLH1	Lactobacillus helveticus	plasmid pLH1	orf195	CAA10964
291	SAu_orf2	Staphylococcus aureus	chromosome	orf	AAG29618
292	LDi_vlf1	Lymantria dispar	chromosome	vlf-1	AAC70272
293	OPs_v1f1	Orgyia pseudotsugata	chromosome	vlf-1	AAC59079
294	SCo_orf2	Streptomyces coelicolor	chromosome	int	CAC08306
295	BBu_orf	Borrelia burgdorferi	chromosome	orf6	AAC34963
296	pNOB8	Sulfolobus sp.	plasmid pNOB8	orf101	T31031
297	pMT1	Yersinia pestis	plasmid pMT1	T1101	T15016
298	ACa_vlf1	Autographica californica	chromosome	vlf-1	AAA66707
299	VCh_orf3	Vibrio cholerae	chromosome	VC0821	AAF96190
300	BMo_vlf1	Bombyx mori	chromosome	vlf-1	AAC63749
301	phi-PV83	Staphylococcus aureus	phage PV83	int	BAA97808
302	PGi_orf	Porphyromonas gingivalis	chromosome	orf6	BAA35089
303	AFu_orf	Archaeoglobus fulgidus	chromosome	AF0082	B69260
304	pCHL1	Chlamydia trachomatis	plasmid pCHL1	orf7	AAA91567
305	pR27	Salmonella typhi	plasmid R27	orf	AAF70020
306	APe_orf	Aeropyrum pernix	chromosome	APE0818	E72674
307	PSy_orf2	Pseudomonas syringiae	chromosome	orfA	CAB96965
			plasmid
308	pNRC100_2	Halobacterium sp.	pNRC100	H0928	T08297
309	MJa_orf2	Methanococcus jannaschi	chromosome	MJ0770	Q58180
310	phi16-3	Rhizobium sp.	phage 16-3	int	CAB54831
311	pCP32-1	Borrelia burgdorferi	plasmid cp32-1	BBP37	AAF07426
312	SAl_orf	Streptomyces albus	chromosome	orf	AAD46512
			plasmid
313	pNRC100_3	Halobacterium sp.	pNRC100	H1373	T08333
314	VCh_orf4	Vibrio cholerae	chromosome	VC0185	AAF93361
315	Tec2	Euplotes crassus	transposon Tec2	orf2B	AAA91341
316	Tec1	Euplotes crassus	transposon Tec1	orf2B	AAA91341
317	PPu_orf3	Pseudomonas putida	chromosome	orf101	CAB54061
318	pCP32	Borrelia hermsii	plasmid cp32	orf6	AAF28881
319	NMe_int	Neisseria meningitidis	chromosome	int	CAB84481
320	pCP32-4	Borrelia burgdorferi	plasmid cp32-4	BBR38	AAF07512
321	pCP18	Borrelia burgdorferi	plasmid cp18	orf6	AAB63432
322	pCP18-2	Borrelia burgdorferi	plasmid cp18-2	orf27	AAF29799
			transposon
323	Tn5401	Bacillus thuringensis	Tn5401	int	P27451
324	SMi_xerD	Streptococcus mitis	chromosome	xerD	CAC19443
325	SPn_xerD	Streptococcus pneumoniae	chromosome	xerD	CAC19448
326	EFa_orf	Enterococcus faecium	chromosome	intD	AAG42074
			phage VT1-
327	VT1	Escherichia coli O157:H7	Sakai	int	BAB19626
328	psiM100	Methanothermobacter wolfeii	phage psiM100	int	AAG39942
329	CP-933C	Escherichia coli O157:H7	phage 933C	Z1835	AAG55933
330	CP-933I	Escherichia coli O157:H7	phage 933I	Z0324	AAG54584
331	CP-933M	Escherichia coli O157:H7	phage 933M	Z1323	AAG55457
332	CP-933U	Escherichia coli O157:H7	phage 933U	intU	AAG57039
333	CP-933T	Escherichia coli O157:H7	phage 933T	intT	AAG56898
334	CP-933N	Escherichia coli O157:H7	phage 933N	intN	AAG55869
335	CP-9330	Escherichia coli O157:H7	phage 933O	intO	AAG56112
336	bIL310	Lactococcus lactis	phage bIL310	orf1	AAK08405
337	bIL311	Lactococcus lactis	phage bIL311	int	AAK08433
338	SPy_orf5	Streptococcus pyogenes	chromosome	int4	AAK34767
339	bIL309	Lactococcus lactis	phage bIL309	int	AAK08349
340	bIL312	Lactococcus lactis	phage biL312	int	AAK08454
341	SPy_orf2	Streptococcus pyogenes	chromosome	int3	AAK33851
342	SPy_orf4	Streptococcus pyogenes	chromosome	int2	AAK34288
343	bIL286	Lactococcus lactis	phage bIL286	int	AAK08288
344	LLa_xerD	Lactococcus lactis	chromosome	xerD	AAK04743
345	LLa_ymfD	Lactococcus lactis	chromosome	ymfD	AAK05330
346	SPy_orf3	Streptococcus pyogenes	chromosome	spy1196	AAK34058
347	SPy_orf1	Streptococcus pyogenes	chromosome	spy0365	AAK33410
348	LLa_orf2	Lactococcus lactis	chromosome	ynbA	AAK05376
349	ECo_orf7	Escherichia coli O157:H7	chromosome	Z4313	AAG58098
350	ECo_orf6	Escherichia coli O157:H7	chromosome	Z1120	AAG55265
351	pMLa	Mesorhizobium loti	plasmid pMLa	mll9356	BAB54967
352	pMLb	Mesorhizobium loti	plasmid pMLb	mlr9649	BAB54839
353	pRi_orf2	Rhizobium rhizogenes	plasmid pRi	ri136	BAB16255
354	MLo_orf1	Mezorhizobium loti	chromosome	mll8495	BAB54366
355	MLo_orf2	Mezorhizobium loti	chromosome	mll7973	BAB53631
356	MLo_orf3	Mezorhizobium loti	chromosome	mlr7741	BAB54140
357	MLo_orf4	Mezorhizobium loti	chromosome	mlr6952	BAB53138
358	SEn_orf2	Salmonella enterica	chromosome	int2	AF261825
359	MLo_orf5	Mezorhizobium loti	chromosome	mll5763	BAB52151
360	ECo_orf8	Escherichia coli	chromosome	ILG1	AAK49816
361	MLo_orf6	Mezorhizobium loti	chromosome	mlr0958	BAB48432
362	CCr_orf1	Caulobacter crescentus	chromosome	CC2681	AAK24647
363	MLo_orf7	Mezorhizobium loti	chromosome	mll4043	BAB50796
364	MLo_orf8	Mezorhizobium loti	chromosome	mll0487	BAB48065
365	MLo_orf9	Mezorhizobium loti	chromosome	mlr0475	BAB48054
366	phi-ETA	Staphylococcus aureus	phage phi-ETA	orf1	BAA97587
367	CCr_xerD	Caulobacter crescentus	chromosome	CC3006	AAK24968
368	CCr_xerC	Caulobacter crescentus	chromosome	CC0344	AAK22331
369	pRVS1	Vibrio salmonicida	plasmid pRVS1	int	CAC35342
370	phiSLT	Staphylococcus aureus	phage phi-SLT	int	BAB21695
371	SSo_xer	Sulfolobus solfataricus	chromosome	xerCD	AAK40704
			transposon
372	CW459	Clostridium perfringens	CW459	int459	AAK17958
373	MPu_xerC	Mycoplasma pulmonis	chromosome	MY5310	CAC13704
374	TVo_xerC	Thermoplasma volcanium	chromosome	xerC	BAB59407
375	TAc_xerC	Thermoplasma acidophilum	chromosome	Tal314	CAC12435
376	TVo_orf1	Thermoplasma volcanium	chromosome	orf1	BAB59869
377	SEn_orf2	Salmonella enterica	chromosome	S020	AAK02039
378	PMu_xerC	Pasteurella multocida	chromosome	xerC	AAK03785
379	PMu_xerD	Pasteurella multocida	chromosome	xerD	AAK02177
380	MLo_xerD	Mesorhizobium loti	chromosome	mlr3575	NP_104652
381	DRa_orf4	Deinococcus radiodurans	chromosome	xerD	AA-F12544
382	HSp_orf1	Halobacterium sp.	chromosome	ssrA	AAG19292
383	PMu_orf1	Pasteurella multocida	chromosome	slpA	AAK03853
384	PGi_xerC	Porphyromonas gingivalis	chromosome	PG1732
385	PGi_xerD	Porphyromonas gingivalis	chromosome	PG0386
386	RCa_orf3	Rhodobacter capsulatus	chromosome	orf	U57682
387	MLo_orf10	Mesorhizobium loti	chromosome	mlr9321	NP_085850
388	MLo_orf11	Mesorhizobium loti	chromosome	mlr9323	NP_085851
389	MLo_orf12	Mesorhizobium loti	chromosome	mlr9324	NP_085852
390	MLo_orf13	Mesorhizobium loti	chromosome	mll9328	NP_085856
391	MLo_orf14	Mesorhizobium loti	chromosome	mll9329	NP_085857
392	MLo_orf15	Mesorhizobium loti	chromosome	mll9330	NP_085858
393	MLo_orf16	Mesorhizobium loti	chromosome	mll9331	NP_085859

In some embodiments, the suitable recombinases are the recombinases listed as numbers 7, 12, 93, 95, 97, and 98 in Table 1.

A method to identify an OSSR is by determining by identifying the catalytic residues. Identifying orthogonality is done by preparing a plasmid containing a gene of interest (such as Kanamycin resistance) that is flanked by putative recombinase recognition sites. Co-transformation of a cell with this plasmid and a plasmid containing the putative recombinase will either result in excision of the gene of interest or no reaction. If a reaction occurs, the cell will then be susceptible to treatment with Kanamycin. This is identifiable by replica plating of viable colonies onto an agar plate containing Kanamycin.

In some embodiments, an integration construct is constructed that can be integrated into a genome using lambda red (a promiscuous recombinase). The integration construct would comprise a promoter blocked by a terminator, with the terminator flanked by recognition sites of one of the six recombinases. By making competent cell stocks of each cell line, each recombinase gene is added as a plasmid and then the activity of the reporter gene is measured. This would determine if each protein was capable of working on multiple sequences.

The paper “DNA recombination with a heterospecific Cre homolog identified from comparison of the pac-c1 regions of P1-related phages” (Sauer and McDermott, Nucleic Acids Research, 2004, Vol. 32, No. 20, 6086-6095; hereby incorporated by reference) performed a similar experiment using a multi-copy plasmid to check cross reactivity between the recombinase Cre and a homolog protein labeled Dre. A marker for Zeomycin resistance was placed between the recognition sites, and then cell lines were transformed with a separate plasmid containing the recombinase under study, either Cre or Dre. By growing these cells in the presence or absence of the antibiotic, a perfect record of viability was reported. When using the non-cross reacting gene, a perfect record of death was reported when using the appropriate gene to remove the resistance marker. This screen addresses point (2) listed above, that a recombinase will not bind to the recognition sites of another. However, this screen does not determine whether a mixed recognition site package (site cre, GENE, site dre, as well as the reverse) is capable of initiating recombination.

The recombinant nucleic acids of the invention can be constructed using methods well known to one skilled in the art. One such method includes the “West Coast BioBricks System” (BioBricks) for which separate constructs have been made for many recognition sites, promoters, resistance markers, and other biological device pieces. These pieces allow sequential assembly of complicated constructs. Exemplary components useful for the BioBricks system are shown in FIGS. 2-9. Coding Sequences (C) are complete open reading frames (type I), or sequences encoding polypeptides but lacking either a stop codon (type II), a start codon (type III), or both (type IV). Ribosome Binding Sites (RBS) are sequences encoding a ribosome binding site, fused 5′ to an ORF part. Terminators (TT) are sequence causing transcription termination.

One can use the BioBricks system to make constructs similar to those described in the referenced paper, with many different recognition sites flanking an antibiotic resistance marker. All relevant combinations will be made for each construct. For example, for recombinases A, B, and C that recognize sites a, b, and c, respectively, the following constructs can be made:

• • a Resistance Marker1a//Resistance Marker 2
  • a Resistance Marker1b//Resistance Marker 2
  • a Resistance Marker1c//Resistance Marker 2
  • b Resistance Marker1a//Resistance Marker 2
  • b Resistance Marker1b//Resistance Marker 2
  • b Resistance Marker1c//Resistance Marker 2
  • c Resistance Marker1a//Resistance Marker 2
  • c Resistance Marker 1b//Resistance Marker 2
  • c Resistance Marker1c.//Resistance Marker 2.

As described above, Marker 1 is removable but Marker 2 is not. Stocks of competent cells are made for each construct. These cells are then transformed with plasmids containing one or more recombinases each to cover all potential combinations. Those plasmids should also harbor resistance marker 3. These transformations are then be plated on agar plates containing antibiotics 2 and 3, and incubated to give rise to resultant colonies. Using the replica plating technique, colonies are then transferred to a plate containing antibiotic 1. Colonies are counted to assess viability.

In some embodiments, the recombinant nucleic acid further comprises a promoter that is upstream of the constructs and is capable of transcribing one or more of the constructs in a suitable host cell.

In some embodiments, the recombinant nucleic acid further comprises one or more target nucleotide sequences that are downstream of the constructs, wherein the one or more target sequences are transcribed when all of the constructs are deleted or excised. The target nucleotide sequences can encode an ORF, interference RNA, antisense RNA, or the like.

In some embodiments, the nucleotide sequence of interest comprises one or more ORF, interference RNA, antisense RNA, or the like, or one or more a terminator, or both thereof.

In some embodiments, the ORF encodes a polypeptide. The polypeptide can be a selective marker, an enzyme, a polypeptide that causes the death of the host cell in which the recombinant nucleic acid is located, or the like.

In some embodiments, each construct can further comprise a terminator located between the nucleotide sequence of interest and the second recognition sequence.

In some embodiments, the construct is located or inserted within two ORFs, that when the construct is excised from the recombinant nucleic acid, the two ORFs form a single ORF encoding a polypeptide of a certain biological function. In some embodiments, the certain biological function is one that causes the death of a host cell comprising the recombinant nucleic acid.

In some embodiment of the present invention, the recombinant nucleic acid comprises a synthetic telomere. The synthetic telomere is one application of multiple OSSRs that function as a counting mechanism for host cell, such as a bacteria, such as E. coli. The synthetic telomere makes use of cell cycle sensitive, low level expression of recombinases that, over time, cleaves inhibitory sequences from the genome, and concludes in the expression of a target gene. Such a device requires OSSRs that do not prevent miscounting, or worse, genomic scrambling. In some embodiments, the synthetic telomere is capable of a time dependence that based on the number of OSSRs present. The recombinases can be used to remove a section of the recombinant nucleic acid, such as DNA. Using the synthetic telomere, nucleotide sequence is removed as it is processed, preventing it from being read or interfering with the counting mechanism.

In some applications of the synthetic telomere, the synthetic telomere can function as a fuse that “burns down” until it reaches its target (i.e., the promoter becomes adjacent or operably linked to a gene or nucleotide sequence) and causes the expression of the gene or nucleotide sequence. The expression of the gene or nucleotide sequence can in turn directly or indirectly cause the activation or up regulation of the expression of one or more genes, and/or the repression or down regulation of the expression of one or more genes.

A synthetic teleomere functions as follows: (1) A suitable signal from the cell causes the transcription of the first recombinase. The second recombinase cannot be transcribed because of the presence of a terminator element. (2) Once the recombinase is translated and folded, the gene for the recombinase and the associated terminator element are excised by a recombination event. This DNA loop will be broken down by the host cell. (3) The next time the initiating signal fires, the second recombinase is transcribed. The third recombinase cannot be transcribed because of the presence of a terminator element. (4) The process repeats until all recombinase-terminator elements have been removed, and a reporter gene at the end of the sequence is expressed.

The synthetic teleomere acts as a time delay between the activation of transcription and the expression of a target gene. However, if the signal pulses are associated with a distinct phenomenon, such as cell cycles, night and day, or chemical washes, the invention now serves as a counting mechanism (albeit one that always counts down).

The present invention also provides for a recombinant vector comprising the recombinant nucleic acid. The recombinant nucleic acid can be a double-stranded or single-stranded DNA, or RNA. In some embodiments, the recombinant nucleic acid is integrated into a chromosome of a host cell. In some embodiments, the recombinant nucleic acid can further comprise sequences sufficient for having the recombinant nucleic acid stably replicate in a host cell. The recombinant nucleic acid can be replicon capable of stable maintenance in a host cell. In some embodiments, the replicon is a plasmid. The present invention also provides for a vector or expression vector comprising a recombinant nucleic acid of the present invention.

It will, be apparent to one of skill in the art that a variety of recombinant vectors can be utilized in the practice of aspects of the invention. As used herein, “vector” refers to polynucleotide elements that are used to introduce recombinant nucleic acid into cells for either expression or replication. Selection and use of such vehicles is routine in the art. An “expression vector” includes vectors capable of expressing DNAs that are operatively linked with regulatory sequences, such as promoter regions. Thus, an expression vector refers to a recombinant DNA or RNA construct, such as a plasmid, a phage, recombinant virus or other vector that, upon introduction into an appropriate host cell, results in expression of the cloned DNA. Appropriate expression vectors are well known to those of skill in the art and include those that are replicable in eukaryotic cells and/or prokaryotic cells and those that remain episomal or those that integrate into the host cell genome.

Selectable markers can also be included in the recombinant expression vectors. A variety of markers are known which are useful in selecting for transformed cell lines and generally comprise a gene whose expression confers a selectable phenotype on transformed cells when the cells are grown in an appropriate selective medium. Such markers include, for example, genes that confer antibiotic resistance or sensitivity.

Methods for introducing the recombinant vectors of the present invention into suitable hosts are known to those of skill in the art and typically include the use of CaCl₂ or other agents, such as divalent cations, lipofection, DMSO, protoplast transformation, conjugation, and electroporation.

Activating expression from the promoter results in the expression of the first recombinase which in turn proceeds to recognize the two recognition sequence of the first recombinase and excise or delete the first nucleotide sequence of interest. Activating expression of each respective recombinase results in the recognition of the two recognition sequence of the respective recombinase and the excision or deletion of the corresponding nucleotide sequence of interest.

In some embodiments, the method further comprises: introducing a recombinant nucleic acid into a host cell prior to the providing step, wherein the recombinant nucleic acid comprises at least the first construct and the second construct.

The present invention further provides for a compositions and methods attenuating signal (non-coding RNA interference and Dominant-Negative complexation) by coupling to the activation of a recombinase, an enzyme which can toggle a DNA element between two states. A target DNA element can be designed to, the difference between the two states is essentially arbitrary and almost unlimited. It is not necessary that the same gene product be produced in both states. When used in traditional systems, these signal attenuation methods are limited by the fact that the intensity of the desired output is directly tied to the level of attenuation. When recombinases are used in traditional systems, they are typically limited by the noise generated in attempting to control the recombinase gene, which can cause the switch to enter the improper state. It has not been previously demonstrated that these various devices can be operated in concert to both: (1) have greater control over the properties of both devices, and (2) produce unique genetic devices that would not be possible without the marriage of these functions.

Non-coding RNA interference is a method of preventing protein expression from a given mRNA. by the introduction of a second, non-coding RNA (hereafter ncRNA) that renders the target mRNA unreadable by the protein synthesis machinery. A number of design styles have been used to demonstrate this, but the key component is that the non-coding RNA typically binds the coding RNA in a 1:1 ratio. Thus, an effect is produced in direct proportion with the number of readable copies, where readable copies=(mRNA−(non-coding RNA)), modulated by the binding constant. This system is itself subject to noise near the equivalence point, but is otherwise a very tuneable system.

Dominant-Negative complexation involves intentional production of a non-functional version of the active enzyme (usually a point mutation in the active site) that attenuates the active enzyme in two ways: (1) Competition for the binding site, and (2) Interference in the formation of functional multimers. In both cases, the level of attenuation is a function of concentration of the active enzyme relative to inactive enzyme. However, in systems where every subunit of a complex must be functional to produce an active enzyme (as with recombinases), the multimer effect allows even small amounts of inactive protein to nullify an otherwise-active complex. The intensity of this effect is increased as the number of monomers required in the active complex grows (recombinases are functional tetramers.) Of particular importance is that the recombinase reaction is fully reversible if it does not go to completion! Therefore, a “mixed” multimer of functional and non-functional monomers will not produce a side-product, but will instead continue to suppress function of active multimers by competing for the binding site.

Recombinases are unique among DNA manipulating enzymes for several reasons: (1) The output of their function is digital. When properly designed, the two states can be assigned any arbitrary function. The intensity or type of activation event has no mandatory influence on the two states in any way. It is even possible to toggle a switch between a “sensitive” and “insensitive” state, so that the output can be made dependent or independent to any other control mechanism. (2) The mechanism of action allows for large numbers of recombinases to be used without concern for exhausting available sites or causing cross reactions between multiple sites. Thus one well-designed circuit could easily be adapted for a different output, and multiple circuits could be used in the same cell. This is important in the construction of logic circuits or decision trees that require multiple events recognized over time before a final state is reached. (3) In addition to not interfering with each other, recombinases have a very limited set of required interactions to perform their function: they need to bind identical monomers and bind to DNA. By not involving any other cellular machinery in their function, the system is simplified and the risk of side reactions and cell overload is reduced.

Two different modes of use are possible, integrated/excised or “facing left”/“facing right”. To simplify, further circuits are described using the “facing left”/“facing right” convention although this system works with both designs. The main difference between the two modes is that integrated/excised is less reversible and thus less likely to be scrambled. However, it functions by removing a DNA element, so genetic information is lost permanently when the switch is activated. Alternatively, the “facing left/facing right” circuit is reusable, but can lead to scrambling of the switch if not properly controlled.

A system, for noise canceling in recombinase circuits, works as follows (FIG. 14):

1. A constitutive promoter is followed by a non-coding, interfering RNA, producing that RNA at a set level.

2. An inducible promoter is followed by a recombinase gene. This mRNA is interfered with by the product of promoter 1.

3. Leaky expression of the inducible promoter does not lead to recombinase expression, and the switch remains “unflipped”

4. Induction of promoter 2 produces recombinase mRNA in sufficient quantity that it cannot entirely be inhibited, and recombinase is produced.

5. The produced recombinase “flips” the switch.

Another system follows a similar plan, but uses a Dominant-Negative enzyme (FIG. 15):

1. A constitutive promoter is followed by an active-site knockout of a recombinase, producing RNA and protein at a set level.

2. An inducible promoter is followed by a functional recombinase.

3. Leaky expression of the inducible promoter does not lead to recombinase function, and the switch remains “unflipped”.

4. Induction of promoter 2 produces recombinase in sufficient quantity that (a) functional tetramers form and (b) can compete with non-functional tetramers for DNA binding sites.

5. The functional recombinase tetramers “flip” the switch.

Note that system requires lower levels of its inhibitory product to cause inhibition. This makes it stronger, but also harder to titrate exact levels. The above two systems allow for noise canceling. By replacing promoter 1 with an inducible promoter, the threshold of activation is no longer a static value, and the amount of induction required for flipping the switch changes based on the cellular environment. This is summarized for both types of systems in FIG. 16. This is an extremely useful and powerful device. The inducible promoters can be of any type, with particular applications that can be tied to the activation and deactivation of different metabolic pathways in the cell because of the sensitivity of measuring relative abundance. The flipping of switches can be tied to growth, or change in carbon or nitrogen source. The systems can be based on either attenuation method.

With careful system construction any two promoters can have an output tied to a change in their expression level ratio rather than in absolute abundance, if they dominant-negative system is used. This is because various ribosome binding sites can be used to alter the relationship between RNA level and protein level to a range where the system responds.

The invention having been described, the following examples are offered to illustrate the subject invention by way of illustration, not by way of limitation.

Example 1

A Fusebox Expression Cassette

An embodiment of the invention is a nucleic acid comprising a nucleotide sequence comprising: promoter—ribosome binding site—recognition site 1a—terminator—recognition site 1b—recognition site 2a—terminator—recognition site 2b—gene of interest, the gene of interest cannot be expressed until the sequence is removed of terminators by treatment with both recombinase 1 and recombinase 2. The expression cassettes for recombinase 1 and 2 do not need to be part of the named construct, nor do they need to be activated simultaneously (hence the name “fusebox”). Once each of the recombinases is activated a single time, it activates a permanent change in cellular state, bringing the cell closer to the expression of the gene of interest. Such a system would allow for multiple, non-simultaneous “checkpoints” to be identified before the gene of interest would be expressed. FIG. 12 shows a representative fusebox expression cassette. A system like this allows for the one-time recognition of multiple signals that result in a permanent change in the cell state. The two (or more) signals do not need to occur simultaneously. This system requires no feedback loop and is low load on the cell.

Example 2

A Synthetic Telomere

FIG. 13 shows a representative synthetic teleomere. This device employs recombinases to catalyze the excision of their own gene from a genomic insert. Only one recombinase can be expressed per promoter cycle, resulting in a change in cell state after a given number of events.

Example 3

Cross Testing of Recombinases and Circuit Design

This example demonstrates the efficacy of the cross testing method, initiation the development of our compatibility grid, and the design a circuit using the information thus gained.

Three of the most commonly used (in recombinant systems) recombinases are tested: cre, dre, and FlpSc (here the Sc annotation means from S. cerevisiae), each paired with one of their better characterized att sites:

lox, acted on by Cre:
(SEQ ID NO: 1)
ATAACTTCGTATAGCATACATTATACGAAGTTAT,
rox, acted on by Dre:
(SEQ ID NO: 2)
TAACTTTAAATAATGCCAATTATTTAAAGTTA,
and
frt:
(SEQ ID NO: 3)
TTTGAAGTTCCTATTCCGAAGTTCCTATTCTCTAGAAAGTATAGG
AACTT.

As multiple sequences for multiple att sites appear across publications, an internal reference code is prepared for each att site. For example, the above sites are referred to as CreA, DreA, and ScA, respectively. This allows keeping track of the various sequences independent of their references while still retaining the reference and sequence information for later publication. It should also be noted that each recombinase has more than a single att site. Most have either two or four, although for commonly used proteins like lox, more are known. These sites need to be cross-tested against each other as well as with att sites that putatively respond to a different recombinase. Such experiments produce independent, non-cross reactive effects across an entire genome with a single enzyme.

Two separate classes of constructs are prepared:

Recombinase constructs: p15A origin, Cm resistance, pTET promoter, and one or two recombinases in an operon.

Att excision constructs: ColE1 origin, Amp resistance, pLacUV5 promoter, attx—Red Fluorescent Protein—atty, where attx and atty are various att recognition sites described above.

These vectors are then co-transformed into E. coli strain DH10B, outgrown for one hour in SOC media, and plated on LB plates containing Ampicillin, Chloroamphenicol, IPTG (to induce RFP expression) and aTc (to induce recombinase expression). Although RFP is induced, the constructs are tested using colony PCR to determine if the corresponding part of the test construct is short, indicating an excision product, or long, indicating that RFP has not been excised. These tests can also be performed using more recombinases and att sites, as well as different copy number of the target plasmid and multiple excision targets, including Kan resistance and removal of a terminator that is blocking beta-galactosidase production (i.e. an “on” switch).

Below, these pairs are drawn out in a grid. The grid is filled in with the expected behavior of each crosstest. Table 2 shows the expected cutting patterns for various combinations of recombinases and att sites.

	TABLE 2
	CreA-	DreA-	ScA-	CreA-	DreA-	CreA-
	CreA	DreA	ScA	ScA	ScA	DreA
Cre	cut	no cut	no cut	no cut	no cut	no cut
Dre	no cut	cut	no cut	no cut	no cut	no cut
FlpSc	no cut	no cut	cut	no cut	no cut	no cut
Cre-Dre	cut	cut	no cut	no cut	no cut	no cut
Dre-FlpSc	no cut	cut	cut	no cut	no cut	no cut
Cre-FlpSc	cut	no cut	cut	no cut	no cut	no cut

As can be see in the right half of Table 2, the absence of cutting on “mis-matched” att sites is critical to the function of our recombinase circuits. While it would be difficult to test greater numbers of recombinases or sites simultaneously, we hope to map out possible conflicts by analyzing each pairwise combination. If future discrepancies arise in more complicated systems, using this information will allow us to more readily identify the cause of the incompatability.

FIG. 14 is a sample gel showing the results the above cross tests. The cross-tests involving Cre, Dre, Cre-Dre and the various site combinations give the expected results quite cleanly by colony PCR analysis. FIG. 14 combines three separate gels and is coded to show the excision behavior of the recombinases on the left when expressed in the presence of the att sites shown above, where those att sites are flanking an RFP production cassette. As standards, there are an unexcisable RFP cassette that can be amplified using the same PCR primers as in the experiment, as well as a “pseudoscar” PCR product that corresponds to the size of a CreA scar after a successful CreA-CreA excision. The PCR primers are universal to the test construct and bind outside of the att sites in order to perform this analysis.

In each set of experiments, the desired behavior is observed. Most importantly, when Cre and Dre are co-expressed, the mixture can correctly excise a CreA-CreA construct, a DreA-DreA construct, but shows no activity on a CreA-DreA construct. This was not necessarily true because the proteins are so similar that antibodies raised to Cre will bind to Dre in a western blot. The exact reason for this relationship is not known, but may have to do with the nature of the Holliday junction resolution (i.e., which nucleotides immediately flank the recombination site) rather than the protein quaternary structure.

A number of cross tests are also performed using FlpSc. Surprisingly, FlpSc is a “bad partner” in crosstests involving Cre. Since FlpSc and Cre are not even in the same sub-family, this behavior is not expected. This result may be related to copy number or att site choice or FlpSc is a less accessible enzyme for advanced circuit design.

The current data of the compatibility grid is in Table 3 below.

	TABLE 3
	CreA-	DreA-	ScA-	CreA-	DreA-	CreA-
	CreA	DreA	ScA	ScA	ScA	DreA
Cre	cut	no cut	some	no cut	no cut	no cut
			cut
Dre	no cut	cut	no cut	no cut	no cut	no cut
FlpSc	some	no cut	cut	no cut	no cut	no cut
	cut
Cre-Dre	cut	cut	no cut	no cut	no cut	no cut
Dre-FlpSc	no cut	cut	cut	N/D	N/D	N/D
Cre-FlpSc	cut	no cut	cut	N/D	N/D	N/D

It currently appears that both Cre and Dre show some cross activity on at least one att site that is normally associated with the other protein. Although it may be possible to work around this problem by using alternate aft sites, other behaviors of FlpSc suggest that screening other recombinases will prove more immediately fruitful. When FlpSc is co-expressed with another protein, we have been unable to obtain a PCR product when we analyze the colonies. FlpSc may be reacting between sites on multiple plasmids, a behavior reported in the literature for Cre and Dre, but this not yet conclusively verified. The inclusion of copy number variation experiments and changing the reporter to Kanamycin resistance and testing for cell survivability, as described previously, may resolve this.

Using the information obtained regarding the compatibilities of Cre and Dre recombinases, an “or” gate is designed as shown in FIG. 15. In this circuit, neither gene A nor gene B can be expressed from their promoters because of the presence of a strong, bi directional terminator in the middle. By differentially expressing either cre or dre, either the white att sites or the striped att sites will excise, respectively. This will allow one of the two target genes to express, but will prevent expression of the other gene by removing its promoter. As described herein, one can control cell fate by differential recombinase expression and can also build towards more complex circuits as additional compatible parings are determined. This circuit for the desired activity can be tested in an agar-plate based assay, where, in the image shown in FIG. 19. The agar-plate based assay comprises the following: Gene A—RFP, Gene B—GFP, promoters in top construct are lacUV5, cre promoter is pTET and dre promoter is pBAD. An agar plate is grown to a lawn, then small disks of filter paper that have been soaked in either aTC (to induce pTET) or arabinose (to induce pBAD) are added to either side of this dish. After diffusion of the inducer, one expects to see a plate as shown below, where no cells produce both fluorescent proteins. As a control, one directly expresses GFP from pBAD and RFP from pTET, in which case the entire plate should express both proteins.

Example 4

New Aft Sites that Make an Orthogonal Pair but Still Respond to an Existing Recombinase

As discussed above, the following describes a method for discovering new att sites that make an orthogonal pair but still respond to an existing recombinase. For example, there are many pairs of sites known that the Cre recombinase can act on, but that the individual sites themselves are not competent to resolve, and thus form exclusive pairs. The information gained from performing the crosstesting work, together with sequence information of the known competent pairs of att sites allows one to determine which residues of the crossover region of the att sites generate this site-match specificity that is independent of the recombinase recognition affinity. Increasing the number of att sites that respond to a single recombinase has great potential for introducing genome-wide modifications in a living organism simultaneously and without side-reactions in response to a single stimulus event. Such a tool would be useful both in optimization of fermentative production of small molecules and in the control of genetically engineered organisms in the field, for example plants that begin breaking down their own cellulose in response to a certain signal.

A primary concern in the use of recombinase based circuits is that since the input signal intensity is effectively decoupled from the output signal intensity (i.e. a different promoter can be used for the recombinase and the target gene, as shown in the “or” gate circuit), there may be problems with noise and fidelity. Unlike traditional promoter systems which respond to a variety of inducer concentrations, a recombinase circuit can be a “single fire” system: as soon as the target DNA sequence is excised (or inverted, in some designs), the new circuit becomes active and typically cannot be undone in a controlled fashion. As such controlling more complex circuits requires compensation for this sensitivity and unidirectional. Allowing the att sites and inverted DNA sections to remain in the cell is more likely to scramble the circuit than to allow for the generation of more intricate pathways. However, since the system is effectively completely irreversible, a mechanism is needed to prevent noisy signal from cutting our circuits. This can be done by expressing dominant negative recombinases along side the functional circuits, as described herein, that is using dominant-negative repression and non-coding RNA interference for tuning recombinase based genetic circuits to allow for decoupling of input and output signal strengths by setting a threshold effect (i.e. band-pass filter).

In a simple system, dominant negative recombinase monomers can be expressed with a constitutive promoter of known output. This drastically reduces the chance that 4 functional monomers can access the target sequence and fire until they are in a concentration in excess of the dominant negative monomers. One then measures the ratio of inactive to active monomers that allows activation. Over time, any circuit could fire regardless of the amount of inactive monomer present, so one can test these constructs in longitudinal experiments to assess their stability, which is especially relevant for field applications. The dominant negative recombinases are expected to be specific for their parent construct. Thus, expressing CreX (where the X signifies the inactive dominant-negative mutant) inhibits the activity of Cre but not Dre, while expressing DreX inhibits the activity of Dre and not Cre. By differentially expressing both CreX and DreX, one is able to set independent thresholds for the activity of each enzyme. This type of behavior is useful for therapeutic applications, where a “tumor-hunter” bacteria must carefully calibrate multiple signals in identifying a tumor before it is allowed to initiate production of a toxic chemical.

In another application, the dominant-negative mutant is put under control of a variable strength promoter, while the active recombinase is also under control of a variable strength promoter. As before, when thee construct is tuned so that the initial active:inactive ratio is below the activity threshold, it will not fire. In this case however, since both promoter strengths are changing, the difference in initial promoter strength can be lower (while protein copy number difference is maintained through differences in ribosome binding site strength). This allows the use of native promoter mechanisms to control a circuit in response to a change in cell physiology. This allows access to more “hands-off” circuits, where a cell responds to natural changes in its own environment rather than induced changes (i.e., adding IPTG or arabinose), and to do so in such a way where a strong response can still be generated by use of the active recombinase causing a much stronger promoter to join up to a target DNA.

This approach is also useful in that, in many circuit designs, one can think of a circuit as being made of “cheap” DNA and “expensive” proteins. In other words, it is energetically costly to maintain a protein gradient of activator and repressor pairs, but energetically cheaper to maintain the DNA that encodes those proteins and the DNA that encodes the target DNA elements they act upon. Since recombinases can induce a permanent change in the DNA of a cell without the constant presence of the protein, circuits can be designed that excise both the recombinase and the dominant negative mutant when they are no longer needed, lowering the protein burden on the cell, and only then expressing the next set of necessary proteins. Using this “sliding window” approach allows the circuit to progress towards completion without an exponential increase in protein production to maintain it.

A knockout of Dre, named DreX(Y324F) is prepared. Tyrosine Y324 is annotated as the active site tyrosine for this enzyme. However, after replacing this residue with phenylalanine, as determined in the sequencing result shown below, one still observes activity of the enzyme using our crosstesting method described herein. See FIG. 20. Activity identical to the native Dre even when DreX(Y324F) is expressed alone. This annotation as the active site residue is incorrect and have moved on to knocking out additional tyrosine residues in Dre, Cre, and FlpSc. This process continues until active site knockouts are identified. One then determines the activation threshold for each pair, determines if the dominant negative pairs are exclusive through crosstesting, and initiates longitudinal studies to determine the fidelity of the thresholds through time.

Example 5

Method of Searching for and Using Orthogonal Site Selective Recombinases

Seven recombinases (Cre, Dre, FlpSc, FlpZb, FlpZf, ΦC31, and Bxb1, where Sc Zb and Zf are different species of yeast) are analyzed for compatibility (ability to act specifically and independently upon their own attachment, att, sites when present in a single cell) in an experimental system (see Tables 4-7). Each is able to produce the desired recombination product using its cognate att sites in our system. Cre is compatible with Dre under some conditions, although some recombination is observed upon sequences flanked by mismatched CreA-DreA att sites (half-sites). This is the only half-site combination that resulted in an excision product. Analysis of the CreA and DreA sites suggest that a functional Holliday junction could be formed, although the identity of the cleavage product has not been determined. Dre and FlpSc are compatible under all conditions, while FlpSc and Cre demonstrated cross-reactivity. The remaining four recombinases show high levels of cross reactivity with non-cognate att sites.

The incompatibility between Cre and Dre is easily resolvable by changing the bases of the crossover region to make CreA and DreA an incompatible pair (one that cannot form a holiday junction that permits strand exchange.) The incompatibility between FlpSc and Cre may not be resolvable, but this pairing (and many additional enzymes and binding sites) is currently being testing using a plate based assay that significantly increases our analytical throughput. A flowchart of this process is shown in FIG. 21.

TABLE 4
	CreA-	DreA-	ScA-	ZbA-	ZfA-	ΦC31B	Bxb1B-
	CreA	DreA	ScA	ZbA	ZfA	ΦC31B	Bxb1B
Cre	12/12	0/12	12/12	12/12	12/12	12/12	12/12
Dre	0/12	12/12	0/12	12/12	12/12	12/12	11/12
FlpSc	10/12	0/11	12/12	8/8	8/8	12/12	10/11
FlpZb	12/12	12/12	12/12	12/12	12/12	12/12	12/12
FlpZf	12/12	12/12	11/12	12/12	12/12	12/12	12/12
ΦC31	12/12	12/12	12/12	12/12	11/12	12/12	11/12
Bxb1	10/12	7/10	10/11	12/12	12/12	12/12	8/8
X/Y - fraction of colonies with observed excision
Bold = desired
Normal = undesired

TABLE 5
Cre and Dre appear to form a highly compatible pair, as do
Dre and FlpSc. FlpSc and Cre cross react, and all other
combinations show a high incidence of background activity. Only
Cre, Dre, and FlpSc are further analyzed for cross-compatability.
X/Y - fraction of colonies with observed excision
Bold = desired
Normal = undesired

TABLE 6
Cross compatability tests are performed by expression
one or two enzymes in the presence of either “full” targets
(2 identical att sites) or “half” targets (2 non identical att sites).
The first 9 boxes are carried over from Table 5.
X/Y - fraction of colonies with observed excision
Bold = desired
Normal = undesired

TABLE 7
The blue shaded boxes show that while Dre does not change it's
behavior under any new conditions, Cre alone is able to recombine
one CreA site + one DreA site. Further analysis of these att sites
suggests a change in the crossover region will resolve this problem.
Cre and FlpSc continue to show cross-cutting behavior in the presence
of Dre. However, neither Cre nor FlpSc show activity on Cre cognate
sites when co-expressed (creA-creA column/Cre-FlpSc row).
X/Y - fraction of colonies with observed excision
Bold = desired
Normal = undesired

While the present invention has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications may be made to adapt a particular situation, material, composition of matter, process, process step or steps, to the objective, spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto.

Claims

1. A recombinant nucleic acid comprising a nucleotide sequence comprising (a) a plurality of constructs comprising a first pair of recombinase recognition sequences which is recognized by a first recombinase, wherein the first pair of recombinase recognition sequences flank a first terminator, and a second pair of recombinase recognition sequences which is recognized by a second recombinase, wherein the second pair of recombinase recognition sequences flank a second terminator, (b) a promoter upstream of the plurality of constructs capable of transcribing the plurality of constructs, wherein each construct independently comprises a nucleotide sequence of interest flanked by a pair of recombinase recognition sequences, wherein each pair of recombinase recognition sequences is recognized by a recombinase that does not cross-react with the recombinase recognition sequences of another construct, and the two recombinase recognition sequences of each pair are oriented in the same direction to each other, and (c) a target gene downstream of the plurality of constructs; wherein the first recombinase and the second recombinase are (i) Escherichia coli Cre and Dre, or (ii) Dre and Saccharomyces cerevisiae FLP.

2. The recombinant nucleic acid of claim 1 wherein each construct independently further comprises one or more genes encoding a recombinase capable of recognizing the pair of recombinase recognition sequences of the construct.

3. A vector comprising the recombinant nucleic acid of claim 1.

4. An ex vivo host cell comprising the vector of claim 3.

5. The recombinant nucleic acid of claim 1, wherein the target gene encodes an open reading frame (ORF), interference RNA, or antisense RNA.

6. The recombinant nucleic acid of claim 5, wherein the target gene encodes the ORF and the ORF encodes a selective marker, an enzyme, or a polypeptide that cause the death of a host cell.

7. The recombinant nucleic acid of claim 1, wherein the nucleotide sequences of interest are terminators.

8. The recombinant nucleic acid of claim 1, wherein each nucleotide of interest comprises (i) an open reading frame (ORF) of a recombinase which recognizes the pair of recombinase recognition sequences flanking the nucleotide of interest, and (ii) a terminator downstream of the ORF.

9. The recombinant nucleic acid of claim 8, wherein the target gene encodes an open reading frame (ORF) and the ORF encodes a polypeptide that cause the death of a host cell.

10. The recombinant nucleic acid of claim 1, wherein the first pair of recombinase recognition sequences flank a first gene encoding the first recombinase wherein the first gene is upstream of the first terminator, and the second pair of recombinase recognition sequences flank a second gene encoding the second recombinase wherein the second gene is upstream of the second terminator.