Construction of long DNA molecules using long PCR-based fusion of several fragments simultaneously.

A procedure for precise assembly of linear DNA constructs as long as 20 kb is proposed. The method, which we call long multiple fusion, has been used to assemble up to four fragments simultaneously (for a 10.8 kb final product), offering an additional improvement on the combination of long PCR and overlap extension PCR. The method is based on Pfu polymerase mix, which has a proofreading activity. We successfully assembled (and confirmed by sequencing) seven different linear constructs ranging from 3 to 20 kb, including two 20 kb products (from fragments of 11, 1.7 and 7.5 kb), two 10.8 kb constructs, and two constructs of 6.1 and 6.2 kb, respectively. Accuracy of the PCR fusion is greater than or equal to one error per 6.6 kb, which is consistent with the expected error rate of the PCR mix. The method is expected to facilitate various kinds of complex genetic engineering projects that require precise in-frame assembly of multiple fragments, such as somatic cell knockout in human cells or creation of whole genomes of viruses for vaccine research.

[1]  J. Yon,et al.  Precise gene fusion by PCR. , 1989, Nucleic acids research.

[2]  Genevieve Pont-Kingdon,et al.  Creation of chimeric junctions, deletions, and insertions by PCR. , 2003, Methods in molecular biology.

[3]  E. Golenberg,et al.  Effect of highly fragmented DNA on PCR. , 1996, Nucleic acids research.

[4]  J. Sninsky,et al.  PCR Applications: Protocols for Functional Genomics , 1999 .

[5]  R. Marusyk,et al.  A simple method for dialysis of small-volume samples. , 1980, Analytical biochemistry.

[6]  T. A. Hall,et al.  BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT , 1999 .

[7]  R. Knippers,et al.  DNA Polymerase II , 1970, Nature.

[8]  M. Stoneking,et al.  Construction of larger-size sequencing templates from degraded DNA. , 1999, BioTechniques.

[9]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[10]  A. Dutriaux,et al.  Gene targeting and somatic cell genetics--a rebirth or a coming of age? , 1999, Trends in genetics : TIG.

[11]  R. Lechler,et al.  Splicing by overlap extension by PCR using asymmetric amplification: an improved technique for the generation of hybrid proteins of immunological interest. , 1997, Gene.

[12]  M. McPherson Directed mutagenesis : a practical approach , 1991 .

[13]  Hideko Urushihara,et al.  PCR-mediated generation of a gene disruption construct without the use of DNA ligase and plasmid vectors. , 2002, Nucleic acids research.

[14]  A. Paul,et al.  Chemical Synthesis of Poliovirus cDNA: Generation of Infectious Virus in the Absence of Natural Template , 2002, Science.

[15]  John M. Sedivy,et al.  Gene Targeting in Human Cells Without Isogenic DNA , 1999, Science.

[16]  A. A. Yolov,et al.  Constructing DNA by polymerase recombination , 1990, Nucleic Acids Res..