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Gene Synthesis by Self-Assembly of Small Oligonucleotide Building Blocks

机译:小寡核苷酸构件的自组装基因合成。

摘要

The invention provides a process for synthesizing genes and other long double stranded polynucleotides by assembling very short oligonucleotides into partly double stranded polynucleotides, and then connecting these partly double stranded polynucleotide subassemblies with linkers comprised of very short oligonucleotides. In one embodiment, the correct order of the polynucleotide subassemblies is coded in overhangs present at each end of the partly double stranded polynucleotide subassemblies. Linkers having a sequence complimentary to the combined overhangs connect adjacent subassemblies, which are then ligated together. In one preferred embodiment the oligos are six bases long, for which there are only 4096 different possible sequence permutations. A complete library of oligos of this size and scale can be cost-effectively synthesized and quality controlled, avoiding the typical errors and yield issues associated with phosphoramidite synthesis of longer oligos. Furthermore, the limited oligo library size supports development of a laboratory-scale gene synthesis machine.
机译:本发明提供了一种通过将非常短的寡核苷酸组装成部分双链多核苷酸,然后将这些部分双链多核苷酸子组件与由非常短的寡核苷酸组成的接头连接来合成基因和其他长的双链多核苷酸的方法。在一个实施方案中,多核苷酸亚组装体的正确顺序被编码在部分双链多核苷酸亚组装体各末端存在的突出端。具有与组合的突出端互补的序列的接头连接相邻的子组件,然后将其连接在一起。在一个优选的实施方案中,寡核苷酸长六个碱基,对于它们,仅存在4096种不同的可能序列置换。可以经济有效地合成和控制质量的这种大小和规模的完整寡核苷酸文库,从而避免了与更长寡核苷酸的亚磷酰胺合成相关的典型错误和产量问题。此外,有限的寡核苷酸文库大小支持实验室规模的基因合成机的发展。

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