Description of a PCR-based technique for DNA splicing and mutagenesis by producing 5' overhangs with run through stop DNA synthesis utilizing Ara-C
© Ailenberg et al; licensee BioMed Central Ltd. 2005
Received: 22 June 2005
Accepted: 01 September 2005
Published: 01 September 2005
Splicing of DNA molecules is an important task in molecular biology that facilitates cloning, mutagenesis and creation of chimeric genes. Mutagenesis and DNA splicing techniques exist, some requiring restriction enzymes, and others utilize staggered reannealing approaches.
A method for DNA splicing and mutagenesis without restriction enzymes is described. The method is based on mild template-dependent polymerization arrest with two molecules of cytosine arabinose (Ara-C) incorporated into PCR primers. Two rounds of PCR are employed: the first PCR produces 5' overhangs that are utilized for DNA splicing. The second PCR is based on polymerization running through the Ara-C molecules to produce the desired final product. To illustrate application of the run through stop mutagenesis and DNA splicing technique, we have carried out splicing of two segments of the human cofilin 1 gene and introduced a mutational deletion into the product.
We have demonstrated the utility of a new PCR-based method for carrying out DNA splicing and mutagenesis by incorporating Ara-C into the PCR primers.
Splicing of DNA molecules is an important task in molecular biology that facilitates cloning, mutagenesis and the creation of chimeric genes. While the advent of restriction enzymes substantially advanced DNA splicing techniques, they cannot be applied universally, and their use is limited to enzyme-specific loci. Other techniques like site-directed mutagenesis by overlap extension [SOE; ], insertional mutagenesis with the megaprimer technique  and staggered reannealing [3, 4] have further improved DNA mutagenesis and splicing. Each method offers advantages and inherent drawbacks. Another cloning approach involving the formation of 5' overhangs utilizes incorporation of nucleotide derivatives into PCR primers [5–7] that stall polymerization. These techniques are dependent on an established set of optimal conditions for strong polymerization arrest, including the correct choice of polymerase or the incorporation of three ribonucleotide derivatives in the primer . Furthermore, chimeric DNA/RNA primers need to be removed and reverse-transcribed in order for the splicing to be completed.
Although in the past we have successfully used the SOE technique for mutagenesis and splicing, we encountered difficulties while constructing larger genes. That led us to develop the staggered reannealing method [3, 4]. This method proved to be useful as well, however, its efficiency declined as the gene to be mutagenized exceeded 1000 bp. Although these techniques allow splicing of any two DNA fragments without the need for restriction enzymes, their efficiency is inversely related to the length of the DNA fragments involved, since these techniques rely on the successful melting and reannealing of DNA to create matching overhangs. We sought to offer an alternative approach to facilitate the splicing of any two DNA segments for mutagenesis and construction of chimeric genes. Our technique utilizes two rounds of PCR, and is based on moderate template-dependent polymerization arrest using cytosine arabinose (Ara-C).
Here we used Ara-C both as DNA polymerase inhibitor and template for DNA mutagenesis and splicing.
Results and discussion
There were a total of 8 PCR reactions that included two Ara-C primers for each of the two segments, and the two polymerases (Taq and Pfu) for each set of primers. PCR products were gel-isolated. At this stage, gel-isolation is essential in order to remove any of the original plasmid that might serve as a template in the second PCR reaction. Alternatively, the original plasmid may be eliminated by digestion with DpnI, although this option is less recommended, since traces of undigested plasmid could affect the outcome of the second PCR reaction. Corresponding segments to be spliced were combined (total of four tubes) and ligated. As indicated above, the rationale for this technique is that Ara-C is a mild polymerization terminator, and therefore it will produce a mixture of cohesive and blunt ends. Hence, the reaction is expected to both terminate (producing sticky ends essential for the splicing phase) and run through the Ara-C (producing blunt ends; this feature is essential to the second PCR reaction). Therefore, lowered concentration of ligase and reduced ligation time were used to optimize conditions to favor cohesive end ligation. The products of the ligase reaction were amplified by the second PCR with Taq or Pfu polymerases using the sense primer A, and the anti-sense primer B, which span the cofilin 1 gene. This PCR reaction produced the expected 552 bp product (blunt end ligation, is expected to produce an extra duplicated piece of DNA of 15 bp). The PCR products were either sequenced directly, or cloned into a plasmid and then sequenced. Based on sequencing results, we observed that incorporation of two Ara-C nucleotides into the PCR primers yielded the expected product. This suggests that the two molecules of Ara-C provided the desired mild termination to produce a product with 5' overhangs, but also allowed the polymerase to run through during the 2nd PCR. Furthermore, based on the design of the primers, the polymerization stalled both after the first and the second Ara-C molecule. Both 5 and 30 min incubations with DNA Ligase were sufficient to preferentially ligate the cohesive ends. This further suggests that two adjacent molecules of Ara-C produce 5' overhangs. Even though both 5 and 30 min ligations were successful in producing the desired product, it is not recommended to allow the reaction to proceed for a prolonged time, nor is it recommended to use high levels of ligase, since these conditions may facilitate blunt end ligation that may produce a mixture of the blunt and cohesive end products. Both Pfu and Taq polymerases were equally capable of producing termination products in the first PCR, while still running through the Ara-C in the second PCR. When one molecule of Ara-C was incorporated in the PCR primers, no termination could be observed, as seen by the addition of a 15 bp segment in the PCR product indicative of blunt end ligation. Even ligation for 5 min in reduced concentration of ligase failed to produce cohesive end ligation when only one Ara-C was employed.
The run through stop method utilizes a novel approach for DNA splicing and mutagenesis. While other mutagenesis techniques like SOE, megaprimer and staggered reannealing create matching overhangs after melting and reannealing, the run through stop method creates matching overhangs by polymerization arrest with Ara-C. We were motivated to design the Ara-C approach because we were not successful in creating gene mutations with the other techniques. Hence, the run through stop offers a good alternative to these techniques.
It has been previously demonstrated that utilizing abasic or RNA nucleotides like tetrahydrofuran derivative or 2-o-methyl ribonucleotide in PCR primers produced 5' overhangs that facilitated cloning of DNA fragments into plasmids [5–7]. These approaches were dependent on strong polymerization termination by the nucleotides. Our technique established the conditions for mild termination of DNA polymerization with two Ara-C molecules. This enables us to use the Ara-C-containing primers in two steps of PCR for DNA splicing and mutagenesis. Although in the present study we used relatively short segments of DNA for proof of principal (~500 bp of the human cofilin gene), this technique, unlike the staggered reannealing technique, is not limited to short DNA fragments. Since both rounds of PCR in the present study are based on conventional PCR, the length limit of the DNA fragments to be mutagenized is that of the PCR technique.
The run through stop method can be summarized in four steps:
1. Amplify two segments of DNA to be spliced using PCR, with phosphorylated primers containing two adjacent molecules of Arabinose nucleotide with overlapping sequence.
2. Gel-isolate the two DNA products, combine and ligate.
3. Amplify the spliced product with flanking primers using PCR.
4. Clone the product into a plasmid.
For the first PCR, 4 primers were designed: Primers A and B flanking the human cofilin 1 gene (Fig 2) and two primers containing Ara-C molecules (Figs 2 and 3)). Primer A-5'-ATActgcagATGGCCGCTGGTGTGGCTGTCTGTG-3'-sense primer of human cofilin 1. Lower case letters represent Pst I sequence and bold letters represent Ala to Ser mutagenesis for down stream usage. Primer Ara-C2-A-5'-GGCATAGCGGCAGTCXXAAAGGTGGCGTAGGGATCG-3'-anti-sense primer that contains two Ara-C molecules (XX) and designed to delete a 20 bp segment from the human cofilin 1 gene (Fig 3). Primer Ara-C2-B-5'-ACTGCCCGTTATGCXXTCTATGATGCAACCTATGAG-3'-sense primer that contains two Ara-C molecules (Fig 3). Additionally, two primers containing only one Ara-C molecule insertion were synthesized. Primer B-5'-CAActcgagGGCTGCCAGATGCTCCAGGCAGG-3'-anti-sense primer of the 3' end of human cofilin 1 gene. Lower case letters represent the sequence for the Xho I gene. In the first PCR, Primer A was used with primer Ara-C2-A, and Primer Ara-C2-B was used with primer B. In the second PCR, primer A was used with primer B (see also Fig 2).
Ara-C primers were phosphorylated for 30 min at room temperature using T4 polynucleotide kinase (Invitrogen, Burlington, ON), followed by inactivation at 65°C for 10 min, and used for PCR with no further purification. PCR was performed with corresponding primers (see above and Fig 2, 3) using 1 U Pfu polymerase (Stratagene, La Jolla, CA) or 1 U of Taq polymerase (Sigma, Oakville, ON), and plasmid pOTB7 containing the human cofilin 1 gene as template (ATCC, Manassas, VA). PCR conditions were as follows: heating to 94°C for 5 min; 40 cycles of: 94°C, 55°C and 72°C each for 30 seconds; final elongation for 7 min. PCR products were gel-isolated using MinElute Plasmid Purification Kits (Qiagen, Mississauga, ON). Corresponding segments to be spliced were combined (total of four tubes) and ligated for 30 min with 400 U, or five min with 200 U of T4 ligase (NEB, Pickering, ON) followed by inactivation for 10 min at 65°C.
Two μl of the ligase reaction were amplified by the second PCR with Taq or Pfu polymerase using the sense primer A, and the anti-sense primer B. Conditions for the second PCR were similar to those of the first PCR. The PCR products were purified (Qiagen). Alternatively, the PCR products were subjected to double digestion with PstI and XhoI followed by ligation into plasmid pcDNA3.1Zeo+ (Invitrogen). One μl of ligation reaction was used to transform 20 μl competent cells (DH5α; Invitrogen), using a short procedure: competent cells were incubated for 5 min on ice, and heat-shocked by immediate plating on pre-warmed (37°C) agar plates. Plasmids were prepared using Fast Plasmid Mini Kit (Eppendorf, Mississauga, ON), and sequenced using the T7 primer.
The products of PCR, as well as the products that were cloned into plasmid pcDNA3.1Zeo+ were sequenced in both directions, utilizing primers A and B, or primer T7, respectively (Hospital for Sick Children).
This study was supported by CIHR grant MOP-15071. NMG was supported by a CIHR M.D./Ph.D. studentship.
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