Assembly pcr

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==Introduction==
==Introduction==
Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).
Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).

Revision as of 13:32, 23 February 2009

back to protocols

Introduction

Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).

Method

Remember that this technique works only if: You want to assembly in series two pieces of DNA from PCR product (or you already have one piece you want to cut out and assemble in series w/ a PCR product; in this case it's easier just to do the PCR for the piece you already have. Believe me, the assembly reaction product is well worth the cost of the extra primers and PCR step).

  • 1) Design the reverse primer for the DNA that will be 5' w/ significant overlap w/ the forward primer for the 3' piece. Essentially, as long as one of the primers has ~20bp overlap w/ the reverse complement of the other primer, the products should anneal in the assembly reaction.
  • 2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.
  • 3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored. Besides, if the residual "middle" primers did create product, they would just be making more starting template!
  • 4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions.
  • 5) Run the product on a gel. If the reaction worked, you should see a band the size of the sum of your two templates.
  • 6) Purify the product (I use the Quiagen PCR pur. kit), cut w/ desired endonucleases, and clone away! The quality of the product from this reaction is usually very good and I can get up to >100 transformants.

by Felix Moser

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