Genome editing has emerged as one of the most exciting new areas of therapeutic development. A variety of tools exist for genome editing. Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 has emerged as the most popular genome editing tool, due to its’ efficiency and ease of use. Co-transfection of Cas9 mRNA with a guide RNA results in a double stranded break that can be repaired by non-homologous end joining (NHEJ), leading to indels that inactivate target genes. If a donor DNA template with homology to the cut site is also co-transfected, homology directed repair can lead to gene correction or insertion.
TriLink offers three types of catalog mRNAs for CRISPR genome editing. For CRISPER/Cas9 gene editing, these include Cas9 mRNA with unmodified bases, as well as Cas9 mRNA modified with 5-methoxyuridine to reduce innate immune responses. We also offer Cas9 nickase modified with 5-methoxyuridine. Cas9 nickase has a D10A amino acid mutation that prevents cleavage of one of the DNA strands. As a result, the Cas9 Nickase generates a single stranded nick instead of a double stranded break. DNA cleavage or editing is directed to a specific chromosomal location by a single guide strand RNA (sgRNA) of ~100 nucleotides. An alternative nuclease for CRISPR is Cas12a. CRISPR/Cas12a gene editing uses a RNA guide strand of ~42 nucleotides. TriLink offers unmodified Cas12a or 5-methoxyuridine modified Cas12a mRNAs.
Included in our gene editing tools are Cre recombinases, a tyrosine recombinase that catalyzes recombination between two loxP sites. Two separate DNA species that both contain loxP sites can undergo a fusion event as the result of Cre mediated recombination. Cre is useful for inserting DNA sequences into genomes that contain loxP sites. It is also useful for cell marking studies in which Cre expression activates an inactive reporter gene flanked by loxP sites in transgenic mouse lines. Cells transfected with Cre mRNA will then express the reporter and reveal which cells were productively transfected.
Clustered regularly interspaced short palindromic repeats (CRISPR) is quickly becoming the most popular tool in the genome editing arena. CRISPR has been adapted for use in mammalian cells from bacterial anti-bacteriophage immune systems.
The TriLink CRISPR tool kit includes two components: the first is a CRISPR nuclease such as Cas9 mRNA or Cas12a mRNA and the second is a guide RNA. In nature, the Cas9 guide consists of a CRISPR RNA (crRNA), as well as a trans-acting CRISPR RNA (tracrRNA). For simplicity and increased potency, researchers fused these two RNAs into a single RNA of ~100 nucleotides, which they called a single guide RNA (sgRNA).
In contrast to Cas9, Cas12a utilizes a single guide RNA of ~42 nucleotides. When Cas9 or Cas12a mRNA and a sgRNA are co-transfected into cells, the guide strand directs the Cas9 or Cas12a protein to a specific location in the genome, where Cas9 then creates a double stranded break. Cas9 Nickase mRNA encodes Cas9 with a D10A mutation, which causes a single stranded nick instead of a double stranded break. This may result in fewer off-target effects.
TriLink offers several mRNAs for CRISPR that are unmodified or modified with 5-methoxyuridine (5moU) to reduce innate immune responses. These have been sequence optimized with the help of leading researchers in the field of optimal expression. When you are ready to move your research to the clinic, TriLink offers cGMP synthesis of guide strands and nuclease mRNAs in our purpose built cGMP facility.
Site specific recombinases are useful tools for the manipulation of genomes, and for conditionally activating or de-activating gene expression in cells and organisms. Recombinases recognize short target DNA sequences of approximately 30-40 nucleotides, and they catalyze directional DNA exchange reactions. Because the recognition sites are not commonly found in the genomes of higher organisms, they can be used as tools to engineer genomes.However, continued expression of a recombinase in a cell or in vivo can result in toxicity and undesired off-target recombination. For this reason, transient expression from mRNA is an ideal method for recombinase expression.
One of the most commonly used recombinases is Cre recombinase. Our CleanCap® NLS-Cre Recombinase mRNA is a capped (Cap 1) and polyadenylated messenger RNA, encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase derived from P1 bacteriophage. Cre catalyzes recombination between two loxP sites, which consist of a 34 base pair recognition site (5' ATAACTTCGTATAGCATACATTATACGAAGTTAT 3'). Cre recombinase has been used extensively to manipulate DNA in plants, bacteria, yeast, and mammals. Depending on the orientation of the loxP sites, Cre can be used to induce DNA cassette exchanges, excisions/insertions, inversions, and translocations.
Applications for NLS-Cre Recombinase mRNA include creation of knock-out or knock-in animals, tissue specific protein expression, and marking studies that report delivery of mRNA to a given cell type. Cre recombinase mRNA is also a useful tool in assessing the efficacy of mRNA delivery in vitro and in vivo.
Transcription Activator-like Effector Nucleases (TALENs) have emerged as a more accessible alternative to zinc-finger nucleases (ZFN). Like ZFNs, TALENs utilize a modular DNA binding motif that can be modified to introduce new DNA binding specificities. Unlike ZFNs, TALENs are not as prone to the sequence context effects that tend to complicate the de novo design, making them a more practical tool for the general scientific community. TriLink custom mRNA transcription service includes TALEN mRNA. A TALEN consists of multiple repeat variable di-residues (RVDs), which each specify binding to a single nucleotide. TALEN arrays are made by stringing together RVDs in a specific order to provide specificity and binding affinity to novel DNA sequences. Commonly, engineered TALEN sequences are fused to non-specific cleavage domains, such as FokI. As with ZFNs, TALENs function as pairs bound to adjacent DNA sequences. TriLink offers mRNA expression vectors that are designed to easily accept a TALEN cloned using the Golden Gate method.
A transposase is an enzyme that catalyzes the movement of a transposon (a DNA element), from one location in a genome to another, in a very precise manner. Transposons are widespread in the human genome, and may be responsible for the rearrangement of as much as 40% of the genome. Transposases were one of the first available tools for inserting exogenous sequences into target genomes. Typically, a sequence designated for transfer is flanked in a transposon cassette by inverted terminal repeats. When the transposon cassette is co-transfected with a transposase mRNA, the transposase catalyzes the excision of the transposon and its insertion into the cell’s chromosome. Two common transposase/transposon systems are Sleeping Beauty and PiggyBac. The Sleeping Beauty transposon integrates into TA sequences in the genome, while PiggyBac inserts into TTAA chromosomal sites.