Enzymatic ligation assisted by nucleases: simultaneous ligation and digestion promote the ordered assembly of DNA
- PMID: 17853876
- DOI: 10.1038/nprot.2007.325
Enzymatic ligation assisted by nucleases: simultaneous ligation and digestion promote the ordered assembly of DNA
Abstract
This protocol describes a method for the one-tube preparative-scale assembly of a specific DNA molecule, the enzymatic ligation assisted by nucleases (ELAN) technique. DNA fragments in ligation reactions are capable of combining to produce numerous products. The ELAN method uses judicious choice of restriction enzyme sites coupled with simultaneous digestion and ligation reactions to create just one product, by converting off-pathway products back into substrate. The experimental parameters critical for a successful ELAN reaction are discussed, and the ordered, one-tube assembly of four DNA fragments in the presence of eight restriction enzymes is demonstrated. This technique will be useful to those performing gene construction, DNA computing, biophysics and even standard molecular cloning. Starting with reactant fragments, the protocol takes 4-16 h to produce nanogram to microgram yields, depending on the complexity of the reaction.
Similar articles
-
Directed assembly of DNA molecules via simultaneous ligation and digestion.Biotechniques. 2007 Jan;42(1):84, 86-9. doi: 10.2144/000112283. Biotechniques. 2007. PMID: 17269489
-
Ligation of nonmatching DNA molecule ends.Plasmid. 1995 Jul;34(1):1-10. doi: 10.1006/plas.1995.1028. Plasmid. 1995. PMID: 7480166
-
One-base excess adaptor ligation method for walking uncloned genomic DNA.Appl Microbiol Biotechnol. 2008 Feb;78(1):173-80. doi: 10.1007/s00253-007-1289-x. Epub 2007 Dec 11. Appl Microbiol Biotechnol. 2008. PMID: 18071644
-
Non-polymerase-cycling-assembly-based chemical gene synthesis: strategies, methods, and progress.Biotechnol Adv. 2008 Mar-Apr;26(2):121-34. doi: 10.1016/j.biotechadv.2007.10.001. Epub 2007 Nov 7. Biotechnol Adv. 2008. PMID: 18068327 Review.
-
[DNA manipulation using artificial restriction enzymes].Tanpakushitsu Kakusan Koso. 2005 Jan;50(1):81-6. Tanpakushitsu Kakusan Koso. 2005. PMID: 15651419 Review. Japanese. No abstract available.
Cited by
-
Advancements in Golden Gate Cloning: A Comprehensive Review.Methods Mol Biol. 2025;2850:481-500. doi: 10.1007/978-1-0716-4220-7_27. Methods Mol Biol. 2025. PMID: 39363089 Review.
-
Advanced Design of Dumbbell-shaped Genetic Minimal Vectors Improves Non-coding and Coding RNA Expression.Mol Ther. 2016 Sep;24(9):1581-91. doi: 10.1038/mt.2016.138. Epub 2016 Jun 30. Mol Ther. 2016. PMID: 27357627 Free PMC article.
-
Advanced Design of Minimalistic Dumbbell-shaped Gene Expression Vectors.Bio Protoc. 2017 Aug 5;7(15):e2425. doi: 10.21769/BioProtoc.2425. eCollection 2017 Aug 5. Bio Protoc. 2017. PMID: 34541152 Free PMC article.
-
Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors.Methods Protoc. 2018 Jul 30;1(3):28. doi: 10.3390/mps1030028. Methods Protoc. 2018. PMID: 31164570 Free PMC article.
-
Universal Template-Assisted, Cloning-free Method for the Generation of Small RNA-Expressing Dumbbell-Shaped DNA Vectors.Mol Ther Methods Clin Dev. 2019 Aug 31;15:149-156. doi: 10.1016/j.omtm.2019.08.008. eCollection 2019 Dec 13. Mol Ther Methods Clin Dev. 2019. PMID: 31660417 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources