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DNA molecular weight standard control, also called DNA marker (ladder), has been widely used in the experiments of molecular biology. In the paper, we report a method by which DNA marker was prepared based on multiple PCR technique. 100–1000bp DNA fragments were amplified using the primers designed according to the 6631~7630 position of lambda DNA. Target DNA fragments were amplified using Touchdown PCR combined with hot start PCR, respectively, followed extracted by phenol/chloroform, precipitated with ethanol and mixed thoroughly. The results showed that the 100–1000bp DNA fragments were successfully obtained in one PCR reaction, the bands of prepared DNA marker were clear, the size was right and could be used as control in the molecular biology experiment. This method could save time and be more inexpensive, rapid, simple when compared with the current DNA Ladder prepared means.
It is necessary to determine the molecular weight (mw) or the base pair (bp) length of nucleic acids in the field of molecular biology. This need encompasses weights or lengths of nucleic acids from sizes ranging from mega bps down to very short oligonucleotides of only a few bp's. Traditionally the base pair length of the nucleic acid has been obtained by comparing the behavior of a nucleic acid under analysis with the behavior of another nucleic acid of defined length and usually but not necessarily of known sequence. Such methods may be electrophoresis, gel filtration chromatography, ultracentrifugation and like methods well known to those in the art. Because of the simplicity of the equipment, ease of use and resolving power to the technique, electrophoresis is the technique most frequently employed to determine the size of nucleic acids.
Double stranded DNA standards were typically prepared from DNA of bacteriophages or plasmids [1, 2]. This process requires the propagation of the virus or plasmid in the appropriate host organism, the purification of the viral or plasmid DNA from the nucleic acids of the host, the digestion of the purified DNA with restriction endonucleases, and the purification of the resulting fragments from undigested DNA and the restriction enzyme. This process was labor, material, and equipment intensive, especially for preparation of large quantities of DNA. Restriction enzyme digested bacteriophage DNA such as Lambda was frequently employed as molecular weight markers. The array of fragment lengths in obtained bp's depended on the nature of the restriction enzyme, the DNA sequence composition, and the conditions employed. Each combination of restriction enzymes, DNA, and conditions provided a unique array of DNA fragments of defined lengths [3, 4].
The polymerase chain reaction (PCR) has been widely applied to the fields of molecular biology, genetics, biochemistry, genetic engineering, forensics, and the like. PCR is a simple, effectively and conveniently method and could prepare amount oligonucleotides in a very short time. However, preparing DNA ladder using common PCR was laborious. Different standard fragments were mixed according to some proportion, which were amplified and concentrated from many PCR products. So, different bands may be a standard to identify and evaluate the length of samples. However, most of DNA ladder had too many bands to be amplified by PCR, respectively, which led to great human resource, material resource, and wealth resource though which was industrialization, industry and sequencing. It is very important to find a new method to produce DNA ladder with a rapid, simple way to reduce costs and improve production. A new way for batch production will be described firstly in this study.
According to the lambda phage DNA sequence (GenBank accession no: J02459), the sequences from 6631–7630bp were selected and covered. The 1 000bp primer represents the region in length from 6631–7630, 900bp primer from 6731–7630, 800bp primer from 6831–7630, 700bp primer from 6931–7630, 600bp primer from 7031–7630, 500bp primer from 7131–7630, 400bp primer from 7231–7630, the 300bp primer from 7331–7630, the 200bp primer from 7431–7630, and the 100bp primer from 7531–7630 of the lambda target sequence. Deoxyoligonucleotides were synthesized using phosphoramidite chemistry and were obtained from Shanghai Sangon Company, China. The primers were shown as in Table 1.
100–1000bp fragments were amplified by multiplex PCR using ten primer pairs in one PCR tube with the same sense primer. The template DNA (15–35ng) was added to a 25μl reaction mixture containing 50mM KCl, 10 mM Tris-HCl(pH 8.3), 2.0mM MgCl2, 75pmol of sense primer, 5pmol of each 100–500bp antisense primer, 10pmol of each 600–1000bp anti-sense primer, 0.3mM dNTPs, and 5 unit of Taq DNA polymerase. Taq DNA polymerase was added using hot start method. PCR was performed using a PxE (Thermo) thermocycler with a temperature profile of 35 cycles, which contained 2 cycles at 95°C for 30s, 56°C for 30s, and 72°C for 1min, 2 cycles 95°C for 30s, 54°C for 30s and 72°C for 1min, 2 cycles for every annealing temperature interval 2 temperature, until 44°C polishing 35 cycles. PCR products were detected by 2% agarose gel with 120V voltages for 40min.
5μl of each PCR reaction mixture was screened on 2% agarose gel electrophoresis and the length was estimated by comparing the known size DNA marker (Sangon), then was purified and sequenced by Sangon Company. The PCR products were extracted through phenol/chloroform and precipitated with ethanol, and then analyzed their UV absorbance under 260nm. 5μl aliquot of the material was electrophoresed and no change in the band migration pattern or band intensities was observed following ethidium bromide staining. The marker was then frozen at −20°C.
All fragments of 100–1000bp were amplified successfully with multiplex PCR way by optimizing process in the PCR reaction system and temperature profile (Figure 1). Finally, with the help of touch down PCR and hot start PCR technique, all the ten DNA fragments were obtained by multiplex PCR. At first, the same amount of ten primer pairs were added to a reaction system, and the annealing temperature profile from 58°C to 48°C for 30 cycles (Figure 1(a)), and the annealing temperature profile from 58°C to 48°C for 35 cycles (Figure 1(b)), 100–500bp fragments were amplified by this method. Adjusting the amount of the ten anti-sense primers and the annealing temperature profile from 56°C to 46°C, most of target fragments were detected. (Figure 1(c)) Finally, raising the amount of 600–700bp anti-sense primers and using the annealing temperature profile from 56°C to 44°C, all the target fragments were amplified and nonspecific fragments disappeared (Figure 1(d)).
PCR has become a widely used tool for detection, identification, and differentiation of pathogenic microorganisms in diagnosis of animal and human diseases or other studies . More and more derived PCR techniques were devised for different study purpose, for instance, multiplex PCR technique, which has been widely used to detect and identify some unknown and possible pathogenic microorganisms in some diseases. Using several primer pairs, each having a particular specificity, in the same reaction added a multidimensional perspective to the diagnostic potential of PCR. Such a procedure allowed simultaneous detection of two or more different microbial agents in a single sample and the inclusion of internal controls. As multiplex PCR involved a far more complex reaction system than the normal simplex mode, so its performance was more difficult to predict and could be assessed only after extensive trials . Thus, quite a number of currently used protocols could be further optimized to exclude nonspecific reactions. In the present paper, ten primer pairs was added to a reaction system to amplify ten different fragments. We optimized the reaction system and reaction to avoid nonspecific reactions and primer dimer, target sequences as defined by primer binding sites had been checked carefully in order to insure high specificity of detection. In addition, using hot start and touch down PCR method, adjusting the quantity of each primer and annealing temperature were available to improve the performance of the amplification reaction. The basic idea of hot-start PCR was to reduce nonspecific amplification in the initial phase by releasing active enzyme only immediately before the first primer binding step . Another kind of PCR, touch down PCR could design a continuous and touchdown annealing temperature range to amplify some fragments . This approach was designed to prevent primer dimer formation, mispriming, and spontaneous initiation of DNA strand synthesis . Finally, with the undisputed success ten fragments based on the multiplex PCR with touch down PCR and hot start were amplified and detected clearly (Figure 1).
Compared with conventional methods for producing DNA Marker, multiplex PCR method could reduce costs and raise production in laboratory once. Undoubtedly the demand for multiplex PCR method is going to increase further purpose in future because of the potential to reduce costs, human and material resource, and raise throughput in the same time for batch production.
This work was partly supported by the grants from the Natural Science Foundation of Henan Province, China (no. 511042300, 624410041) and Science & Technology Innovation Talents in University of Henan Province (2008HASTIT026).