Cloning of double-stranded DNA (dsDNA) molecules into plasmid vectors is one of the most commonly employed techniques in molecular biology. The procedure is used for sequencing, building libraries of DNA molecules, expressing coding and non-coding RNA, and many other applications. Past Core Concepts articles in DECODED, available online at www.idtdna.com/DECODED, have reviewed the Gibson Assembly™ method and cohesive-end cloning techniques. There you will also find additional information on plasmid basics in the article: Cloning strategies, Part 2: Cohesive-end cloning, which may be of benefit to readers of this article. Here we will discuss blunt-end cloning as a third method by which DNA fragments can be cloned into a plasmid vector.
Blunt-end cloning overview
Blunt-end cloning involves ligating dsDNA into a plasmid where both the insert and linearized plasmid have no overhanging bases at their termini. It does not benefit from the hydrogen bond stabilization associated with the complementary overhanging bases used in cohesive-end cloning, but the transient associations of the available 5’ phosphate and 3’ hydroxyl groups are sufficient to produce successful clones in the presence of T4 ligase . An illustration of a basic blunt-end cloning experiment is shown in Figure 1.
Blunt-end cloning is also one of the easiest and most versatile methods for cloning dsDNA into plasmid vectors. It is easy because the blunt-ended insert requires little to no preparation—avoiding the enzymatic digestion and subsequent purification needed for cohesive-end cloning. It is versatile because insert and vector have fewer sequence limitations than other methods. This means that blunt-end cloning has some unique advantages, and also disadvantages, over cohesive-end cloning and isothermal assembly methods.
There are several factors that make blunt-end cloning challenging. It is 10–100X less efficient than cohesive-end cloning, resulting in fewer colonies; and half of these recombinant colonies have inserts incorporated in the wrong orientation. In addition, a lot of plasmid re-circularization occurs. It can be reduced, but is not easily eliminated, resulting in a lot of empty vectors. Therefore, when using this method, you should screen by restriction digestion or PCR prior to sequence-verification.
A major advantage of blunt-end cloning is that the desired insert does not require any restriction sites in the sequence. This makes blunt-end cloning extremely versatile, simplifies planning, and avoids unwanted, artificial sequence additions that might adversely affect some applications. Also, because the insert does not need to be prepared by restriction digestion, blunt-end cloning has the potential to be significantly faster.
Tips for successful blunt-end ligations
Preparing the vector
The vector can be prepared by digestion if the multiple cloning site (MCS) contains a recognition site for a restriction enzyme that produces blunt ends, such as EcoRV (Figure 1). Restrictions sites that generate sequence overhangs can also be used, followed by removal or filling of the overhangs to create blunts ends. However, this approach is not recommended since there is no good method for assessing the success of the blunting reaction, making it hard to troubleshoot unsuccessful reactions.
Alternatively, linearized plasmid can be prepared for blunt-end cloning by amplification with a high-fidelity polymerase and subsequent PCR using primers designed with their 5’ ends at the desired insertion site. The linearized plasmid product appears as a distinct band on an agarose gel, compared to a smear produced by the supercoiled plasmid template, facilitating troubleshooting. The circular template plasmid is eliminated by digesting with DpnI, or a similar restriction enzyme, that cuts the methylated plasmid leaving the unmethylated PCR product.
The plasmid is typically dephosphorylated for ligation and amplification methods. However, it is possible to avoid this requirement (see alternative below).
Designing the insert
The blunt-ended insert needs to be phosphorylated. If you plan to anneal oligonucleotides or use IDT gBlocks® Gene Fragments as your insert, note that these are not synthesized with 5’ phosphate groups unless requested—make sure to select the 5’ phosphate option when ordering these sequences for blunt-end cloning. Alternatively, phosphates can be added to the 5’ ends of dsDNA with a simple kinase reaction, for example using the commercially available T4 Polynucleotide Kinase. However, this method is less efficient, particularly when bases other than G are kinase targets.
When the ends of the insert are not blunt, a polishing or filling reaction is required. Examples of ends that need polishing or filling include inserts generated by shearing or sonication, or by Taq polymerase, which preferentially leaves a single adenosine overhang at the 3’ ends; inserts produced by restriction digests; and some inserts produced by annealing multiple oligonucleotides to create longer products. A number of DNA polymerases will remove DNA overhangs and/or can be used to fill in missing bases if there is a 3’ hydroxyl available for priming. Polymerases for such reactions include T4 DNA polymerase, PFU, and the Klenow Fragment of DNA polymerase I. There are many options and kits available so check with the manufacturers to determine which one works best for your application.
As with other cloning methods, shorter inserts will usually ligate more efficiently than longer ones. Manufacturers typically include size recommendations for plasmid inserts in the plasmid documentation as a useful guide in planning your cloning experiment.
Finally, unlike cohesive-end cloning, blunt-end cloning does not automatically recreate a restriction site following ligation of the insert unless bases are added to the insert sequence to complete the missing site (Figure 1). Figure 1. Blunt-end cloning using dephosporylated vector. (A) In this example, the vector is linearized by EcoRV to produce blunt ends. The insert was derived from 2 hybridized DNA oligonucleotides with optional bases to reproduce the EcoRV on one end, shown in orange. The required 5’ phosphates are shown as blue circles. (B) The ligated bases form a single, new EcoRV site that can be re-cut at one end. The other end has only half of the original restriction recognition site and can no longer be digested by EcoRV. Because the EcoRV site is palindromic, there is a 50% chance that the recreated site occurs at either end of the MCS.
In blunt-end ligations, the association of 5’ phosphate groups and 3’ hydroxyl groups is more transient than in cohesive-end ligations. Because they lack the hydrogen bond stabilization of cohesive ends, blunt-end ligations are more sensitive to reaction conditions, especially to the concentrations of the reaction components.
The likelihood of an insert associating with a linearized plasmid is increased by having a high concentration of available insert blunt ends. However, the intramolecular circularization of the plasmid, after one end of the insert has been joined, works best at lower concentrations. Insert concentrations that are too high, or overall DNA concentrations that are too high, can result in plasmids with multiple inserts, or concatemers. Although it is not always necessary, some researchers perform a short 1hr incubation with high concentrations of insert and ligase, then dilute the reaction 20X with ligase buffer and allow the ligation to proceed for 4 more hours in order to facilitate the second step in the ligation reaction .
T4 ligase quality and concentration are also important. Blunt-end ligations typically take place in the presence of higher concentrations of ligase than cohesive-end ligations. For example, whereas a cohesive-end ligation may use 1 unit T4 ligase/20 μL reaction, a blunt reaction may use up to 3 units/20 μL reaction. Commercially available T4 ligases typically state whether they are optimized for blunt-end ligations or not. Follow the manufacturer’s guidelines to determine which ligase is appropriate for your cloning experiment and what concentration to use. Note that Taq ligase as well as several other ligases do not ligate blunt ends.
An alternative blunt-end method
As was mentioned, unless the insert is designed with the necessary bases to recreate the restriction site, the blunt restriction site used to linearize the vector is not normally recreated by the ligation of the insert (Figure 1). This allows for an alternative, less common, blunt-end cloning method that does not require the vector to be dephosphorylated. Instead, it relies on competing digestion and ligation reactions to decrease empty vector background.
In this method, the circularized plasmid and insert are placed in a reaction mixture containing the blunt-end−producing restriction enzyme, as well as the T4 ligase. The circular plasmid is cut and the insert ligated in a single tube reaction. Empty plasmid that is produced by T4 ligation is subsequently re-cut by the restriction enzyme. As long as the insert is not designed to produce that specific restriction site, all circularized plasmids should contain the desired insert. Specifics for this method—also described with a polishing enzyme component—can be found in Sambrook and Russell . One reason why researchers may want to avoid this technique is that it involves mixing multiple optimized enzyme buffers, which may adversely affect the activity of individual enzymes. Check with the enzyme manufacturer(s) to determine if your chosen enzymes are compatible with this method.
- Sambrook J and Russell DW, editors. (2001) Molecular Cloning: A Laboratory Manual. 3rd ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory.
Product focus—dsDNA fragments and useful buffers gBlocks® Gene Fragments are double-stranded, sequence-verified genomic blocks up to 2000 bp in length that can be shipped in 2–8 working days for affordable and easy gene construction or modification. gBlocks fragments are synthesized using the same industry-leading, high-fidelity synthesis chemistries developed by IDT for Ultramer™ oligonucleotides, and are sequence verified prior to shipping. Using the isothermal assembly method, 4 gBlocks fragments can be assembled into a multi kb gene in less than 1 hour; a simple, 30 nt sequence overlap is required when designing the gene fragments.
Learn more about gBlocks Gene Fragments
IDTE 1X TE Buffers are ideal for resuspension, dilution, and storage of DNA for research purposes, including DNA oligos, gBlocks Gene Fragments, and plasmid DNA used for molecular cloning. IDTE buffers contain 10 mM Tris, pH 7.5 or 8.0, 0.1 mM EDTA and are available in 1 L, 10 x 2 mL, 300 mL, or 4 x 1 L sizes.
Buffers are guaranteed to be nuclease-free. Each lot is tested using our RNaseAlert™ and DNaseAlert™ reagents to document the absence of detectable nuclease activity. Individual lots are screened for endotoxins using a Limulis Abocyte Lysate (LAL) assay.
Learn more about IDTE 1X TE Buffers
Cloning strategies, Part 1: Assembly PCR for novel gene synthesis—Learn about this flexible technique that uses single-stranded oligos or a mix of single- and double-stranded DNA to produce longer genes of up to several thousand bp. Tips for reaction conditions and reagent preparation are included to facilitate successful cloning experiments.
Isothermal assembly: Quick, easy gene construction—In a single reaction, isothermal assembly combines several overlapping DNA fragments to produce a ligated plasmid ready for transformation, Find out how isothermal assembly works, how to use of this strategy to simplify construct building, and pick up some experimental design suggestions.
Cloning strategies, Part 2: Cohesive-end cloning—Cloning of double-stranded DNA (dsDNA) molecules into plasmid vectors using restriction digestion is one of the most commonly employed techniques in molecular biology. The procedure is used for sequencing, building libraries of DNA molecules, expressing coding and non-coding RNA, and many other applications. Here we describe considerations for cohesive-end cloning experiments.
Read an example for how gBlocks Gene Fragments are used in Building biological factories for renewable and sustainable products,or browse the current content of our online DECODED newsletter.
Author: Hans Packer is a scientific writer at IDT.
© 2012, 2016 Integrated DNA Technologies. All rights reserved. Trademarks contained herein are the property of Integrated DNA Technologies, Inc. or their respective owners. For specific trademark and licensing information, see www.idtdna.com/trademarks.