T1 zinc fingerbased knockout punches for zebrafish genes. A potential answer comes from zinc finger nucleases zfns which have been demonstrated to efficiently block the activity of a gene by cleaving the human genome at a predetermined site and altering the genetic sequence via an errorprone dna repair process. One zinc finger binding domain recognizes and binds to a three nucleotide sequence, one can thus increase the binding specificity of a zfn by adding more zinc fingers. A novel tale nuclease scaffold enables high genome editing activity in. A zinc finger nuclease, transcription activatorlike effector nuclease, or laglidadg homing endonuclease transgene is transformed into. However, the factors that affect zfn protein stability and function are not yet clear. Recently, it has been shown that targeted mutagenesis using zincfinger nucleases zfns and transcription activatorlike effector nucleases talens can be used to generate knockout zebrafish lines for analysis of their function andor developing disease models. Zincfinger nucleases zfns are powerful tools for experimental gene manipulation. Plants developed by zfn3 european food safety authority. Zincfingers are small dnabinding proteins that mediate dnaprotein interactions within cells, playing an important role in regulation of dna expression. Rapid mutation of endogenous zebrafish genes using zinc finger. Zebrafish danio rerio is a fresh water fish that inhabits rivers in india, pakistan and other places in asia.
Efficient methods for targeted mutagenesis in zebrafish using zinc. Zinc fingerbased knockout punches for zebrafish genes. Zinc finger nucleases zfns, chimeric fusions between dnabinding zinc finger proteins and the nonspecific cleavage domain of the foki endonuclease, hold great promise for targeted mutagenesis in zebrafish, as demonstrated by two recent publications doyon et al. Here we describe a detailed protocol for constructing zfn expression vectors, for generating and introducing zfnencoding rnas into zebrafish embryos, and. It is one of three methods of changing the genome with engineered nucleases they have two parts. Zebrafish foxp2 zinc finger nuclease mutant has normal. Enhancing zincfingernuclease activity with improved. Construction and evaluation of zinc finger nucleases.
The former pages history now serves to provide attribution for that content in the latter page, and it must not be deleted so long as the latter page exists. Significantly, several of these new lines have been used to reveal novel. Mosaic g0 injected fish were identified using high resolution melt analysis hrma pcr of somatic dna finclip, and we describe our use of hrma pcr for screening and identification of mutants. However, the size of the zebrafish genome, the relatively long generation time, and. The schematic diagram of safety and toxicity testing of nutraceuticals by using the crisprcas system in zebrafish. Zinc finger nucleases zfns are a class of engineered dnabinding proteins that facilitate targeted editing of the genome by creating doublestrand breaks in dna at userspecified locations. The dna cleavingdomain fok 1 nuclease can then be used to create a doublestranded break in dna at the desired point fig. Each of these zfn pairs induces targeted insertions and deletions with high efficiency at its endogenous gene target in somatic zebrafish cells.
Zinc finger protein motif that forms a compact globular structure that coordinates one or more zn ions. The generation of genetically modified animals or plants with genetargeted deletions or modifications is a powerful tool to analyze gene function, study disease and produce organisms of economical interest. From an archive of 27 different zinc finger modules, we assembled more than 70 different zinc. The plant genome original research genome engineering of. We appreciate as much detail as possible and references as appropriate. Recent advances in genome engineering using zinc finger nucleases zfns and transcription activatorlike effector nucleases talens have facilitated the creation of targeted gene knockout mutations in zebrafish. Background customized zinc finger nucleases zfns form the basis. Zinc finger nucleases or zfn are a tool used to target genes and change dna. In principle these technologies are capable of targeting virtually any site in. Zinc fingers are manmade molecules made of a protein and zinc. Your guide to investing in zincfinger zfn gene editing if youre an investor whos heard of zincfinger proteins and gene editing but you arent sure what it all means, this can help answer. The diverse combinations and functions of zinc finger motifs make zinc finger proteins versatile in biological processes, including development, differentiation, metabolism and autophagy. Zinc finger nucleases zfns allow targeted gene inactivation in a wide range of model organisms.
Using open, we successfully engineered zfn pairs for five endogenous zebrafish. Precise genome modification in the crop species zea mays. Zfns are also used to create a new generation of genetic disease models called isogenic human disease models. The dna binding motif specified by the zinc fingers directs the zfn to. N2 the ability to manipulate the genome is critical to develop and test hypotheses based on genetics. Zincfinger nucleases zfns are artificial restriction enzymes generated by fusing a zinc finger dnabinding domain to a dnacleavage domain.
Targeted mutagenesis in zebrafish using customized zinc finger. There are various options for designing and assembling zfn and. Zfns induce a targeted doublestrand break in the genome that is repaired to generate small insertions and deletions. Here, we adapt this technology to create targeted mutations in the zebrafish germline in vivo. Stability of zinc finger nuclease protein is enhanced by. Your guide to investing in zincfinger zfn gene editing.
This approach is an outcome of the zinc finger consortium, a collaboration across multiple academic labs interested in promoting the application of zfps as a research tool. In the past two decades, zebrafish has become one of the preferred in vivo model organisms for studying diverse processes like embryogenesis 8, 9, autophagy, behaviour 11, 12 and sleep. Zfns are artificial restriction enzymes that cause doublestranded breaks at defined points within the genome. Zebrafish is a powerful model for the study of vertebrate development. Using zinc finger nucleases for efficient and heritable. By taking advantage of endogenous dna repair machinery, these reagents can be used to. Zincfinger nucleases make the cut in hiv to control hiv. In most vertebrate model systems direct genomic manipulation at a specific locus is still not feasible. Our zinc finger nuclease zfn technology is based on a naturally occurring class of proteins called zinc finger dnabinding proteins zfps, which recognize and bind to specific sequences of dna. Text andor other creative content from this version of zinc finger nuclease was copied or moved into zinc finger nuclease treatment of hiv with this edit. However, construction of targetspecific zfns is technically challenging.
Zinc finger nuclease an overview sciencedirect topics. Zinc finger proteins are the largest transcription factor family in human genome. Zfns consist of an engineered array of zinc fingers fused to the nonspecific foki nuclease domain and function as. You may not transfer the product, its components, or any materials made through the use of this product, including modified animals, to any third party without prior written approval of sigma and without the transferee entering into a material transfer agreement with sigma. Please use this form to recommend updates to the information in zfin. However, one drawback that limits the utility of this model organism is the lack of technology to efficiently generate targeted mutations in genes of interest. Microinjection and homologous recombination inembryonic stem es cells, are robust but overallinefficient.
The scope for improvement of yield and disease resistance of crop plants by genetic engineering has been limited by the lack of an efficient method. Part of the methods in molecular biology book series mimb, volume 11. Label license agreement zinc finger nuclease zfn 2. To facilitate the application of zfns within the zebrafish community. Targeted mutagenesis in zebrafish using customized zinc. Foley je, yeh jr, maeder ml, reyon d, sander jd, peterson rt, joung jk 2009 rapid mutation of endogenous zebrafish genes using zinc finger nucleases made by oligomerized pool engineering open. Background zinc finger nucleases zfns are powerful tools for gene therapy and genetic engineering. Only a few percent of the injected eggs giving rise totransgenic animals. Heritable targeted gene disruption in zebrafish using.
Zinc finger nucleases zfns provide a system to introduce genomic lesions at a specific site in vertebrate cell lines. Zinc finger proteins in cancer progression journal of. Zfns were engineered that recognize sequences in the zebrafish ortholog of. The european commission requested that the efsa panel on genetically modified organisms deliver a scientific opinion related to risk assessment of plants developed using the zinc finger nuclease 3 technique zfn3 which allows the integration of genes in a predefined insertion site in the genome of the recipient species. Zinc finger engineering the zinc finger consortium. The characterization of zfn protein stability and the development of simple methods to improve zfn function would facilitate the application of this promising technology.
There is a need to develop more genetic tools for approaching new species along with the model organisms. Recently, zebrafish has sparked interest in other branches of the biomedical research. Zebrafish danio rerio is a fresh water fish that inhabits rivers in india, pakistan. Zfn proteins and their recognition sites within the zebrafish kdrl and. Wolfgang wende, toni cathomen, alfred pingoud, a novel zincfinger nuclease platform with a sequencespecific cleavage module. Pdf genome editing in zebrafish using highfidelity cas9. A dnabinding domain comprised of a chain of twofinger modules, each. Efficient methods for targeted mutagenesis in zebrafish. The world now has two major technologies for targeted editing of the genome. Genome editing in zebrafish using highfidelity cas9 nucleases.
Here, we evaluate a straightforward modular assemblybased approach for zfn construction and gene inactivation in zebrafish. The consortium is committed to developing resources, software, and other tools for engineering zinc fingers and for performing genome engineering that are robust, userfriendly, and publicly available. Zinc finger nuclease zfn technology has recently been introduced to the zebrafish system as a complementary reverse genetic strategy to induce targeted mutations. A number of recent papers have shown how this technology can be applied effectively to models of human gene therapy. Zincfinger nucleases zfns allow targeted gene inactivation in a wide range of. The nucleases used in our platform provide high specificity and optimized digestion conditions possible. Until recently, the generation of animals with gene targeted manipulations has been accomplished by homologous recombination hr in embryonic stem es cells or cloning through. Evaluation and application of modularly assembled zinc. Significant target genes and useful methods of zfn delivery have been reported. The dsb is induced by a zinc finger nuclease zfn4,5, which is a designed, sequence specific endonuclease that can be customized to cleave a userchosen dna target. Consensus sequence 2 cys held in beta sheet and 2 his in alpha helix tetrahedrally coordinated to zn ion.
Targeted gene inactivation in zebrafish using engineered. Based on our advanced techniques and rich experience, creative biolabs provides zincfinger nuclease service for our global clients, especially those who are currently working on drug target validation. Genome editing with engineered zinc finger nucleases. In this example, the sequence of events for producing a targeted mutant are shown. Zinc finger nucleases as tools to understand and treat. Zinc finger nuclease that disables ccr5 gene may offer potential new hiv treatment approach. In the study published in science titled knockout rats via embryo microinjection of zinc finger nucleases, geurts, et al. Researchers create first targeted knockout rats using zinc. Each zinc finger nuclease zfn consists of two functional domains. In this paper we generated and screened zinc finger nucleases zfns against zebrafish foxp2 using a modified bacterial 1hybrid screen. Pdf zincfinger nucleases zfns allow targeted gene inactivation in a wide range of model organisms. Zinc finger domains can be engineered to target desired dna sequences and this enables zincfinger nucleases to target unique sequences within complex genomes.
A zfn is a hybrid molecule that couples the dna binding domain of a zincfinger protein with the dnacleaving nuclease domain of the restriction endonuclease foki. One of the more advanced selectionbased design strategies currently in use is referred to as the open oligomerized pool engineering design 18,19. Engineered zinc finger nucleases zfns are broadly useful and powerful reagents for genome manipulation 1 6. Zinc finger nuclease that disables ccr5 gene may offer. Zincfinger nucleases zfns are programmable nucleases that have opened the door to the genome editing era. This is not an easy task and it is a great challenge for comparative biology. Over the last few decades, increasing evidence reveals the potential roles of zinc finger proteins in cancer progression. We engineer zfns for precision, efficiency, and specificity, which we believe are the critical. The easiest type of editing to do with a zfn is to inactivate a gene, says dana carroll. This biological diversity and evolutionary pathways are recognized by comparing organisms with available model organisms. Zinc finger nucleases are useful to manipulate the genomes of many plants and animals. New emerging tools such as crispr and zinc finger nucleases allowing.
A novel zincfinger nuclease platform with a sequencespecific cleavage module benno schierling. Targeted mutagenesis in zebrafish using crispr rnaguided. Zinc finger nuclease technology market report offers accurate regionwise market projections and forecasts, market share, size, segmentwise analysis, regulatory framework assessment, opportunities and challenges for stakeholders, and impact of key industry trends. We describe here the use of zinc finger nucleases zfns for somatic and germline disruption of genes in zebrafish danio rerio, where targeted mutagenesis was previously intractable. The construction of zfns recognizing a target sequence of interest is laborious, and has not been widely used recently. This video provides a brief description of how zincfinger nucleases function and can be utilized to alter a dna of interest. Zincfinger nucleases zfns drive efficient genome editing by introducing a doublestrand break into the targeted gene. A zfn designed to create a dna doublestrand break dsb in the target locus is composed of two. This modification of the cellular dna is permanent and can fully block gene function. In this video we discuss zinc finger nucleases, which are an important tool for cutting dna. Choosing the right nuclease for the task chapter pdf available in methods in molecular biology clifton, n. Zinc finger simple english wikipedia, the free encyclopedia. Zincfinger nucleases zfns are enzymes got by fusing a zinc finger to a dna cleavage enzyme called a fokl.
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