CSTZFN
CompoZr® Custom Zinc Finger Nuclease (ZFN)
ZFN plasmid and mRNA
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General description
Application
- Creation of gene knockouts in multiple cell lines
- Complete knockout of genes not amenable to RNAi
- Creation of knock-in cell lines with promoters, fusion tags or reporters integrated into endogenous genes
- Creation of cell lines that produce higher yields of proteins or antibodies
Features and Benefits
- Rapid design, assembly, and validation of a ZFN pair targeting your gene of interest
- Rapid and permanent disruption of, or integration into, any genomic loci
- Mutations made are permanent and heritable
- Works in a variety of mammalian somatic cell types
- Edits induced through a single transfection experiment
- Knockout or knock-in cell lines in as little as two months
- Single or biallelic edits occur in 1-20% of clone population
- No antibiotic selection required for screening
Components
- Best Performing ZFN Pair
- 10 Aliquots of Ready-to-Deliver ZFN Pair in mRNA form
- ZFN Pair in Plasmid Form
- Forward and Reverse Primers that allow for determination of rate of mutation and for screening of individual clones
- Positive Control DNA
- Used to determine a baseline cutting efficiency
Other Notes
Custom ZFN Service offering HERE
Legal Information
related product
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
Certificates of Analysis (COA)
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What is a Zinc Finger Nuclease (ZFN)?
A ZFN is a hybrid molecule that couples the DNA binding domain of a zinc-finger protein with the DNA-cleaving nuclease domain of the restriction endonuclease FokI. The DNA binding motif specified by the zinc fingers directs the ZFN to a specific (targeted) locus in the genome.
Why are these sometimes referred to as ZFN pairs?
A pair of ZFNs is required to cleave double-stranded DNA. This is a requirement of the FokI nuclease. FokI must dimerize to achieve a double strand break in the DNA. You will be provided with a pair of ZFNs for your target site that has been validated to cut at the endogenous chromosomal locus in a proxy cell line.
What specificity should be expected from a ZFN?
Due to the dimerization requirement of the FokI endonuclease, a pair of ZFNs is required to cause a double strand break. This strategy requires two different ZFNs to bind at the target site. Each ZFN recognizes a different 12-18 base pair target sequence, and these target sequences must be separated by 4-7 base pairs to allow formation of the catalytically active FokI dimer. These positional constraints drive a very high degree of specificity.
Will a ZFN knockout a gene in my cell line?
Yes. ZFNs for gene knockout typically target within the ORF of coding exons. The ZFN that is delivered to you for gene knockout will cause a targeted double strand breakage (DSB) in the genome of your cells. After the DNA is cut by the ZFN, the cell repairs the breakage by the natural process of non-homologous end joining (NHEJ). This is an imperfect repair process that usually results in the loss or gain of genetic information (typically tens of base pairs) at the site of the DSB. Due to the mutations caused by ZFN-mediated NHEJ, 1-20% of resulting clones are expected to have both copies of the target gene knocked out.
Will a ZFN insert a gene into my cell line?
Yes. To achieve targeted gene integration you must co-transfect your ZFN with a repair template, consisting of the gene to be inserted flanked by genomic sequence engineered to match (i.e., be homologous to) the sequence surrounding the intended ZFN cut site. After your ZFN cuts at the site specified by its sequence, the natural mechanism of homology dependent repair (HDR) takes over. The cell will recognize the homologous sequence in the repair template and insert the exogenous gene at the site of ZFN cleavage.
What is the best way to deliver the ZFN and the repair template into the cells?
The ZFN itself can be delivered as a plasmid or it can be transcribed into an mRNA transcript for delivery. We have found both plasmid and mRNA to be effective depending on cell type and, therefore, provide customers with ZFNs in both plasmid and mRNA form to test in their own cell lines. Repair templates are typically delivered into the cell as linear DNA. Regardless of form, mRNA, DNA, or plasmid, we have found that the use of nucleofection or electroporation generally produce the highest DNA cleavage efficiencies. Due to this increase in efficiency, we recommend using an electroporation or nucleofection delivery method if possible. Lipid-based transfection also works in many cases, but may result in lower efficiencies.
How is the binding specificity of the ZFN tested?
The binding specificity of the zinc finger modules in the Sangamo archive have previously been characterized by a number of in-vitro methods (ELISA among others).
How has the cleavage ability of my ZFN been tested?
To test the cleavage ability of the ZFNs we use a mismatch-specific nuclease assay. In this assay, PCR primers are used to amplify across the ZFN cleavage site in genomic DNA extracted from ZFN-treated cells. The resulting PCR products, which are now a mixture of wild type and mutated amplicons, are then denatured and re-annealed. When wild type and mutant alleles of the PCR products re-anneal with each other a mismatch occurs. The fragments are then exposed to a mismatch-specific nuclease and the digested reaction is run on a gel to look for smaller migrating cleavage products that indicate cleaved mismatches. The smaller migrating cleavage products reflect the frequency of mutated alleles and are a measure of in vivo ZFN efficacy. Quantitation of the released fragments allows a calculation of the percentage of mutated genes in the population.
In which cell lines/organisms do the ZFNs work?
Sigma has a standard offering of ZFNs for Human, Mouse, and Rat. We expect the ZFN technology to work in most organisms. For instance, ZFNs have recently been shown to produce site-specific gene knockouts in Zebrafi sh (Doyon et al., Nature Biotechnology., May 25, 2008). The ZFNs for this particular application were tested in a yeast proxy system that accurately reflects ZFN activity in many other cell types.
I have a cell line I created by using a ZFN to knockout a gene. I would like to knockout a second gene in this cell line. Is this possible?
Yes, this is definitely a possibility. It has been shown that at least 3 different genes could be successively knocked out of the genome in the same cell line.
Can every gene be targeted by a ZFN?
Yes. Using our current library of 2-finger zinc finger modules, we believe we can produce a working ZFN for about every 200 bp on average, making genome wide coverage feasible. We plan to continue updating our library of zinc finger modules to increase the genomic coverage.
Should I expect off-target effects from my ZFN?
The ZFN reagents that we provide are unlikely to cause significant offtarget effects. The proprietary algorithm that Sigma uses to design the candidate ZFNs targets only sites that are unique within the genome. This, as well as the use of specially engineered obligate heterodimer FokI cleavage domains (Miller et al., Nature Biotechnology, July 25, 2007), helps guard against off-target effects for the ZFN you receive.
My cell line is very hard to transfect. Can I still use ZFNs?
Efficiency of delivery is very important. We have had great success with viral delivery of ZFNs, including AdV, AAV and lentivirus. If you have a viral delivery system available, then we can give guidance on how to apply it to the use of ZFNs.
Do the ZFNs remain in the cells after causing desired mutations?
No. The ZFNs are only expressed transiently but the genetic alteration is permanent. The transient nature of ZFNs also reduces the possibility of off-target effects.
When using Product CSTZFN, CompoZr® Custom Zinc Finger Nuclease, ZFN,do I need to use a selection marker for Targeted Gene Integration?
In many cases the efficiency of Targeted Gene Integration is >1% - even without selection. So selection markers are often not necessary. However, in certain circumstances, selection might be useful to have, e.g., when working with poorly transfectable cells.
Can Zinc Finger Nucleases be synthesized to a specific mitochondrial DNA sequence?
This is target dependent, however the simple answer is yes- as long as sequence content is fairly diverse with some GC content. There is already literature for targeting of mtDNAs with ZFNs.
Can Zinc Finger Nucleases be cloned in an inducible promoter?
Yes, though we don't have any examples or data around this. It is effectively a typical expression cassette so there should not be a problem. However, there are several potential outcomes. If a pair of catalytically active ZFN expression cassettes are stably integrated into a genome, any "leaky" expression could result in premature gene editing. Additionally, we should also consider the fact that we have no control over the type of modification incurred at the ZFN target site (assuming no donor is introduced). The outcomes might include small insertions and deletions resulting in frameshift (like we want) or it could result in an in-frame modification that may not necessarily yield functional gene knockout.
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