Li Mamie Z, Elledge Stephen J
Howard Hughes Medical Institute, Department of Genetics, Harvard Partners Center for Genetics and Genomics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA.
Nat Methods. 2007 Mar;4(3):251-6. doi: 10.1038/nmeth1010. Epub 2007 Feb 11.
We describe a new cloning method, sequence and ligation-independent cloning (SLIC), which allows the assembly of multiple DNA fragments in a single reaction using in vitro homologous recombination and single-strand annealing. SLIC mimics in vivo homologous recombination by relying on exonuclease-generated ssDNA overhangs in insert and vector fragments, and the assembly of these fragments by recombination in vitro. SLIC inserts can also be prepared by incomplete PCR (iPCR) or mixed PCR. SLIC allows efficient and reproducible assembly of recombinant DNA with as many as 5 and 10 fragments simultaneously. SLIC circumvents the sequence requirements of traditional methods and functions much more efficiently at very low DNA concentrations when combined with RecA to catalyze homologous recombination. This flexibility allows much greater versatility in the generation of recombinant DNA for the purposes of synthetic biology.
我们描述了一种新的克隆方法——序列与连接无关克隆(SLIC),该方法利用体外同源重组和单链退火,可在单一反应中组装多个DNA片段。SLIC通过依赖核酸外切酶在插入片段和载体片段中产生的单链DNA(ssDNA)悬端来模拟体内同源重组,并通过体外重组来组装这些片段。SLIC插入片段也可通过不完全聚合酶链式反应(iPCR)或混合PCR制备。SLIC能够高效且可重复地同时组装多达5个和10个片段的重组DNA。SLIC规避了传统方法对序列的要求,并且在与RecA结合以催化同源重组时,在极低的DNA浓度下也能更高效地发挥作用。这种灵活性使得在合成生物学中用于生成重组DNA时具有更大的通用性。