Deletion mutagenesis of large areas in Plasmodium falciparum genes: a comparative study
© Williams et al; licensee BioMed Central Ltd. 2007
Received: 05 February 2007
Accepted: 22 May 2007
Published: 22 May 2007
The increasing emergence of Plasmodium falciparum parasites resistant to most of the cost-effective drugs has necessitated the identification of novel leads and drug targets. Parasite-specific inserts in enzymes that are essential for the differentiation and proliferation of malarial parasites have received considerable interest since it distinguishes these proteins from their human counterparts. The functions of these inserts, which include mediations of protein activities or protein-protein interactions, are being investigated by several strategies including deletion mutagenesis. A comparative study of five widely used PCR-based mutagenesis methods identified a modified inverse PCR method as particularly suitable for the deletion of large areas (>100 bp) in malaria parasite genes.
The restriction enzyme-mediated inverse PCR method described here incorporates unique restriction enzyme sites at the 5'-ends of inverse tail-to-tail primers. The entire gene-containing vector is amplified except the desired region to be deleted and cloned using the unique restriction sites to increase ligation efficiency. This method was compared in its efficiency to delete a ~400 bp parasite-specific insert in malarial S-adenosylmethionine decarboxylase/ornithine decarboxylase (PfAdoMetDC/ODC) to existing PCR-based site-directed deletion mutagenesis methods including the QuickChange™ site-directed mutagenesis, ExSite™, overlapping primer and inverse PCR. In addition, the modified method was applied in the deletion of a >600 bp parasite-specific insert in another malarial gene, pyridoxal kinase (PfPdxK).
The modified and optimized restriction enzyme-mediated inverse PCR method resulted in 80% compared to 40% deletion mutagenesis efficiency of the overlapping primer method in the deletion of a large area (411 bp) from a large malaria gene (PfAdoMetDC/ODC, gene size 4257 bp). In contrast, deletion mutagenesis methods such as the well-known QuickChange™ site-directed mutagenesis, ExSite™ and inverse PCR methods produced insignificant results. A 100% mutagenesis efficiency was obtained with the restriction enzyme-mediated inverse PCR method to delete 618 bp from a smaller gene (PfPdxK, gene size 1536 bp).
An efficient method was developed for the deletion of large areas (>100 bp) in significantly sized genes such as those of the A+T-rich P. falciparum genome.
Specialized organisms like Plasmodium falciparum have unique adaptations, which include generally larger protein sizes compared to orthologues due to bifunctional arrangements of proteins and the presence of parasite-specific inserts . In general, these inserts are species-specific, rapidly diverging, non-globular regions containing low-complexity areas consisting of mainly Lys and Asn residues that form flexible prion-like domains extending from the protein core [2, 3]. Up to 90% of P. falciparum proteins contain at least one low-complexity region, which may co-localize with parasite-specific inserts. These proteins are also up to 50% longer compared to their yeast counterparts [4, 5]. The exact evolutionary origin and functional advantages of these inserts remain elusive. It has, however, been proposed by Karlin et al  that these inserted regions are adaptive as they seem to promote protein-protein interactions and mRNA stability. For example, in P. falciparum it has been demonstrated that stabilization of interdomain interactions of the bifunctional malarial drug target, dihydrofolate reductase (DHFR)/thymidylate synthase (TS), is mediated via an essential parasite-specific insert [7, 8]. DHFR/TS also regulates its own translation by binding to cognate mRNA . Some parasite-specific inserts have been implicated in malaria pathogenesis due to an increase in the antigen diversity and resultant incomplete immune response of the human host to P. falciparum .
In this study, a restriction enzyme (RE)-mediated inverse PCR is described that successfully removes large areas in abnormally large genes (gene size ~4.3 kb). The deletion mutagenesis efficiency of this RE-mediated inverse PCR method was compared to the existing methods described above by deleting a 411 bp parasite-specific insert in the AdoMetDC domain of the bifunctional PfAdoMetDC/ODC protein. In addition, its application to delete an insert in another malarial gene was also investigated.
Primers used for the various mutagenic protocols. The Bam HI restriction sites for primer pairs P3 and P4 are underlined. The P3 primer pair was used with and without Bam HI restriction digestion for the RE-mediated inverse PCR and inverse PCR methods, respectively.
Primer Sequence (5' to 3')
QuickChange™ site-directed method
gatagtagtgatgctgat ↓ aattataataaggagagctttttatataatg
Overlapping primer method 
gctttccttattataatt ↓ atcagcatcactactatcataaagctttaaattatcc
ExSite™, inverse  and RE-mediated inverse PCR methods
RE-mediated inverse PCR method
QuickChange™ site-directed mutagenesis (QCM)
According to the manufacturers' recommendations, a 50 μl reaction contained 10 ng template (0.002 pmol for the 7.4 kb template used here), 125 ng of each of the primers (8.8 pmol each of A3consF and R), 1 × Pfu reaction buffer, 200 μM of each dNTP, and 2.5 U Pfu DNA polymerase (Fermentas, Burlington, Canada). The temperature cycles were as follows: incubation at 95°C for 30 sec, followed by 30 cycles of 95°C for 30 sec, 55/60°C for 1 min, 68°C for 2 min/kb and a final extension at 68°C for 2 min/kb.
ExSite™ PCR-based site-directed mutagenesis
The PCR reaction with a final volume of 25 μl was set up as follows: 0.5 pmol template, 15 pmol of each primer (A3reF and R), 1 × Pfu reaction buffer, 200 μM of each dNTP, and 2.5 U Pfu DNA polymerase (Fermentas, Burlington, Canada). The temperature cycles were as follows: incubation at 94°C for 4 min, 50°C for 2 min, 68°C for 2 min/kb of template, followed by 18 cycles of 94°C for 1 min, 56°C for 2 min, and 68°C for 1 min/kb, followed by a final incubation at 68°C for 5 min.
Overlapping primer method
A typical deletion mutagenesis reaction for the overlapping primer protocol with a final volume of 50 μl, contained 50 ng template (0.01 pmol for the 7.4 kb template), 2 pmol of each primer (A3overF and R), 1 × Pfu reaction buffer, 200 μM of each dNTP and 2 U of Pfu DNA polymerase (Fermentas, Burlington, Canada). The cycling parameters were 94°C for 3 min, 16 cycles of 94°C for 1 min, 52°C for 1 min and 2 min/kb at 68°C with a final extension for 1 hour at 68°C according to the method described by Zheng et al .
Inverse PCR method
The PCR reaction set up followed the protocol as indicated by Wang et al . A typical deletion mutagenesis reaction with a 50 μl final volume contained 50 ng template (0.01 pmol for the 7.4 kb template), 150 ng of both primers (15 pmol of A3reF and R), 1 × Pfu reaction buffer, 200 μM of each dNTP and 2.5 U Pfu DNA polymerase (Fermentas, Burlington, Canada). The temperature cycles were as follows: 95°C for 3 min, 18 cycles of 95°C for 45 sec, 62°C for 1 min and 68°C for 2 min/kb, with a final extension at 68°C for 2 min/kb. The same reaction was also repeated with the addition of 5% DMSO.
RE-mediated inverse PCR method
For the RE-mediated inverse PCR method described here a typical deletion mutagenesis reaction with a 50 μl final volume contained 50 ng template (0.01 pmol for the 7.4 kb template), 150 ng of both primers (15 pmol each of A3reF and R), 1 × Pfu reaction buffer, 200 μM of each dNTP and 2.5 U Pfu DNA polymerase (Fermentas, Burlington, Canada). The temperature cycles were typically as follows: 95°C for 3 min, 18 cycles of 95°C for 45 sec, 56°C (Table 1) or 62°C for 1 min and 68°C for 2 min/kb, with a final extension at 68°C for 2 min/kb . The abovementioned conditions were chosen for comparative purposes to the other methods. However, follow-up experiments have shown a 105 molar excess of primer:template to be optimal (template concentrations ranging from 0.01 pmol to 0.15 fmol with 15 pmol primer). In addition, 2.5 U ExTaq (TaKaRa Biomedicals, Shiga, Japan) was used on this larger template.
The effectiveness of this method in deleting a parasite-specific insert  in another A+T rich P. falciparum gene was also tested. The P. falciparum PdxK gene (gene size ~1.5 kb) was cloned into the same pASK-IBA3 vector (total template size ~4.6 kb) . The reaction conditions as well temperature cycles were identical as given above.
Analysis of mutagenesis products
PCR products were analysed with 1% agarose electrophoresis to determine if the correct sized mutant products were obtained. Correctly sized PCR products were subsequently treated with 10 U of Dpn I for 3 hrs at 37°C to remove parental templates. For the restriction-mediated inverse PCR method, 10 U Bam HI (Fermentas, Burlington, Canada) was additionally added to the Dpn I digestion in a dual compatibility buffer Tango™ (33 mM Tris-acetate pH 7.9, 10 mM Mg-acetate, 66 mM K-acetate and 0.1 mg/ml BSA). Products were purified with the HighPure PCR product purification kit (Roche Diagnostics, Mannheim, Germany) and ligated for 16 hrs with 3 U of T4 DNA Ligase (Promega, Wisconsin, USA) at 4°C. The resulting circular plasmids were transformed into electrocompetent DH5α cells (Gibco BRL, Life Technologies, USA). Five clones for each of the three different mutagenesis methods that produced PCR products were analysed with Hind III restriction mapping. In the wild type gene, this enzyme should cut twice resulting in three bands of ~3900, ~3100 and ~450 bp. However, in the ~400 bp deletion mutants, one of the sites is removed resulting in only two bands sized ~3900 and ~3100 bp. These same clones were thereafter analysed with nucleotide sequencing to confirm the mutagenesis results. Application of the restriction-mediated inverse PCR method on the deletion of ~600 bp from the PfPdxK gene also resulted in a PCR product. Five clones were analysed with Eco RI restriction mapping. The deletion removes an Eco RI site resulting in the linearization of only the wild type nonmutated DNA (~4.6 kb template).
Deletion mutagenesis efficiency results for the different protocols used. Five clones were analysed for each of the different PCR-based mutagenesis methods based on duplicate PCR experiments.
PCR product analysed with agarose gel electrophoresis
Restriction enzyme mapping with Hind III
Deletion efficiency confirmed with nucleotide sequencing (%)
QuickChange™ site-directed method
Overlapping primer method
Inverse PCR method
RE-mediated inverse PCR method
RE-mediated inverse PCR method
Eco RI linearization site removed
Due to the ever-increasing resistance of malarial parasites to commercially available drugs, it is of extreme importance to identify novel drug targets. Studies of the essential P. falciparum AdoMetDC/ODC bifunctional protein have led to the development of the RE-mediated inverse PCR method reported here. This enabled investigations of the structure-activity relationships of the large parasite-specific inserts of this bifunctional protein.
The RE-mediated inverse PCR method was compared to four other widely used PCR-based mutagenesis methods. The QuickChange™ site-directed mutagenesis method (QCM) requires that both of the mutagenic primers contain the desired mutation and anneal to the same sequence on opposite strands of the plasmid. The method is limited to primers of 25 to 45 nt in length with melting temperatures approximately 10°C above the extension temperature of 68°C. The mutation should preferably be in the centre of the primer flanked by at least 10 bases on either side. The GC content must also be at least 40%, and the primers must terminate in a G or a C base, which is difficult when working with the A+T-rich genome of P. falciparum. The QCM method claims 80% efficiency for point-mutagenesis but was unsuccessful in this deletion mutagenesis study. This also explains the inconsistent results produced in this laboratory by application of the QCM deletion mutagenesis method for the deletion of significantly sized areas in various other malaria genes .
The ExSite™ PCR-based site-directed mutagenesis method uses higher template concentrations and reduced PCR cycles to minimize potential second-site mutations. Primers for this method must be greater than 20 bases in length. The mismatched portions of the primers should be at or near the 5'-terminus of one or both of the primers with 15 or more of the matching sequence at the 3'-terminus. One or both of the primers must be 5' phosphorylated. In order to make a specific mutation, the alteration must be included within the primers and their 5'-termini must meet but not overlap. Any bases between the 5'-termini will subsequently be deleted in the final product. The application of the ExSite™ method did not result in any product.
Zheng and his co-workers modified the QCM protocol by using primers with partial overlaps at the 5'-termini to prevent self-extension (overlapping primer method, ). This method was applied to vectors of up to 12 kb in length and yielded significantly improved PCR mutagenesis results. The modified primers were proposed to overcome the limitation of the melting temperature of primer design dictated by QCM. At least 8 non-overlapping bases must be present on the 3'-termini of the primers, and the mutations may be as close as 4 nt away from the 5'-terminus. The primers must also terminate in a G or a C residue. The overlapping primer method was reported to delete up to 7 bp  and had a 40% mutagenesis efficiency in deleting 411 bp from the ~7.4 kb template in this study.
Inverse PCR employs two inverted tail-to-tail primers to amplify an entire gene/vector except for the region that needs to be deleted. This method has been successful in deleting up to 102 bp in large plasmids (12 kb) . According to Wang et al., for this method to be effective the primers must be similar in size, between 30 and 45 nt in length and have a melting temperature of at least 78°C with an applied annealing temperature of 68°C . The number of PCR cycles must also be preferably less than 20. The application of this method produced the expected 7 kb deletion product as judged by gel electrophoresis only in the absence of DMSO. However, the correct deletion product was not present in any of the 5 clones screened (Figure 3, lane 3). The primary causes for such background after PCR-based mutagenesis techniques could include the mis-priming and subsequent generation of incorrect, transformation-competent PCR products or the self-annealing of the 5'-overhanging CGC ends of the primers that could prevent subsequent blunt-ended ligation . The results presented here support other examples which suggests that a maximum of only 12 bp can be removed with the inverse PCR method .
The RE-mediated inverse PCR method is a straightforward method in which the primers do not require either 5' phosphorylation or purification by PAGE or HPLC as specified by the general inverse PCR protocol . Large deletions can be made without increasing the length of the primers as the desired mutation is not incorporated into the primer sequence itself but is simply deleted by extending the plasmid during the PCR reaction. A further advantage of this method is that the PCR temperature cycles of less than 20 are needed, which decreases the incidence of DNA polymerase error rates. The method was not dependent on the addition of 5% DMSO (results not shown) as is often needed by the inverse PCR method for the prevention of secondary structure formation in both primers and template. Additionally, there is no requirement for a high primer GC content as with the QCM method, which again is useful with the A+T-rich P. falciparum genome. Primer options for QCM and inverse PCR are furthermore limited by the fact that the melting temperature of the primers must be ≥ 78°C, which was not the case in the RE-mediated inverse method.
The inability in deleting a reasonably large (>100 bp) DNA region with existing oligonucleotide-based deletion mutagenesis methods led to the application of a highly efficient RE-mediated inverse PCR method for the deletion of large areas in abnormally large P. falciparum genes. The method incorporates unique restriction enzyme sites at the 5'-ends of inverse tail-to-tail primers. In the absence of unique restriction sites, alternative methods including DiSec/TriSec , which allows the generation of specified sticky-ends, may be used or a restriction-independent method like the overlapping primer method should suffice. The method has proven to be invaluable in deciphering the involvement of parasite-specific inserts in structure-activity relationships of PfAdoMetDC/ODC and PfPdxK (manuscript in preparation).
This work was supported by the National Research Foundation (NRF) of South Africa and the University of Pretoria. Any opinion, findings and conclusions or recommendations expressed in this paper are those of the author(s) and therefore the NRF does not accept any liability in regard hereto.
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