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TA Cloning

TA Cloning is a subcloning technique that doesn't use restriction enzymes[1] and is easier and quicker than traditional subcloning. The technique relies on the ability of adenine (A) and thymine (T) (complementary basepairs) on different DNA fragments to hybridize and, in the presence of ligase, become ligated together. PCR products are usually amplified using Taq DNA polymerase which preferentially adds an adenine to the 3' end of the product. Such PCR amplified inserts are cloned into linearized vectors that have complementary 3' thymine overhangs. Commercialized kits with pre-prepared vectors and PCR reagents are currently sold, greatly speeding up the process.


Creating The Insert

The insert is created by PCR using Taq DNA polymerase. This polymerase lacks 3' to 5' proofreading activity and, with a high probability, adds a single, 3'-adenine overhang to each end of the PCR product [2]. It is best if the PCR primers have guanines at the 5' end as this maximizes probability of Taq DNA polymerase adding the terminal adenosine overhang[3]. Thermostable polymerases containing extensive 3´ to 5´ exonuclease activity should not be used as they do not leave the 3´ adenine-overhangs[4].

Creating the Vector

The target vector is linearized and cut with a blunt-end restriction enzyme. This vector is then tailed with dideoxythymidine triphosphate (ddTTP) using terminal transferase. It is important to use ddTTP to ensure the addition of only one T residue. This tailing leaves the vector with a single 3'-overhanging thymine residue on each blunt end[5]. Manufacturers commonly sell TA Cloning "kits" with a wide range of prepared vectors that have already been linearized and tagged with an overhanging thymine residue.

Benefits and Drawbacks

Given that there is no need for restriction enzymes other than for generating the linearized vector, the procedure is much simpler and faster than traditional subcloning. There is also no need to add restriction sites when designing primers and thus shorter primers can be used saving time and money. In addition, in instances where there are no viable restriction sites that can be used for traditional cloning, TA cloning is often used as an alternative. The major downside of TA cloning is that directional cloning is not possible, so the gene has a 50% chance of getting cloned in the reverse direction [1].


1. ^ a b "Improved TA Cloning". Caister Academic Press. http://www.caister.com/molecular-biology-blog/2009/06/improved-ta-cloning.html. Retrieved 2009-10-17.
2. ^ "TA Cloning". Premier BioSoft. http://www.premierbiosoft.com/tech_notes/TA_Cloning.html. Retrieved 2009-10-17.
3. ^ "TA cloning protocol". Durham, New Hampshire, USA: Hubbart Center for Genomic Studies. http://hcgs.unh.edu/protocol/basic/Cltaclone.html. Retrieved 2009-10-17.
4. ^ "TA Cloning Kit Manual". Invitrogen. 7 April 2004. pp. 31. http://stanxterm.aecom.yu.edu/wiki/data/Product_manuals_attach/ta.pdf. Retrieved 2009-10-17.
5. ^ Holton, T.A.; Graham, M.W (1991-03-11). "A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors". Nucleic Acids Research 19 (5): 1156. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC333802/pdf/nar00241-0176.pdf.

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