Department of Biomedical Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ.
Curr Protoc. 2021 Nov;1(11):e278. doi: 10.1002/cpz1.278.
Genome DNA sequencing has become an affordable means to resolve questions about the genetic background of life. However, the biological functions of many DNA-encoded sequences are still relatively unknown. A highly scalable and cost-effective cloning method to select natural DNA targets from genomic templates is therefore urgently needed to enable rapid understanding of the biological products of genomes. One such method involves LASSO probes, which are long single-stranded DNA oligonucleotides designed with a universal adapter that is used to link two sequences that are complementary to a genomic target of interest. Through a pooled assembly method, LASSOs can be made for multiplex DNA capture. Herein, we describe a robust, efficient method to assemble LASSO probe libraries using a Cre-recombinase-mediated reaction and a protocol for multiplex genome target capture. The starting components are a pre-LASSO probe library comprising short DNA oligo pools designed in silico and an Escherichia coli plasmid (pLASSO) that incorporates the pre-LASSO library. Through internal recombination of pLASSO with its inserts, a mature LASSO library in final configuration can be made with high purity. Assembly of a LASSO probe library takes 4 days, and target capture can be performed in a single day. With an exponentially growing list of new genomes available for investigation, this method can enable the rapid production of ORFeome libraries for high-throughput screening to identify biological functions as a complementary approach to understand genome functional biology. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Assembly of LASSO probes Support Protocol 1: Generation of pLASSO vectors Support Protocol 2: Preparation of pre-LASSOs Basic Protocol 2: Massively parallel capture of large DNAs using LASSO probes.
基因组 DNA 测序已成为一种经济实惠的手段,可用于解决有关生命遗传背景的问题。然而,许多 DNA 编码序列的生物学功能仍然相对未知。因此,迫切需要一种高度可扩展且具有成本效益的克隆方法,以便从基因组模板中选择天然 DNA 靶标,从而能够快速了解基因组的生物学产物。一种这样的方法涉及 LASSO 探针,它是设计有通用接头的长单链 DNA 寡核苷酸,该接头用于连接与感兴趣的基因组靶标互补的两个序列。通过池组装方法,可以进行 LASSO 的多路复用 DNA 捕获。在此,我们描述了一种使用 Cre 重组酶介导的反应和多重基因组靶标捕获协议来组装 LASSO 探针文库的稳健,高效的方法。起始成分是包含短 DNA 寡聚池的预 LASSO 探针文库,这些寡聚池是在计算机上设计的,并且包含在大肠杆菌质粒(pLASSO)中。通过 pLASSO 与其插入物的内部重组,可以以高纯度制成最终构型的成熟 LASSO 文库。组装 LASSO 探针文库需要 4 天,并且可以在一天内完成靶标捕获。随着可供研究的新基因组数量呈指数增长,这种方法可以快速生成 ORFeome 文库,用于高通量筛选以鉴定生物学功能,作为理解基因组功能生物学的补充方法。©2021Wiley Periodicals LLC。基本方案 1:组装 LASSO 探针支持方案 1:生成 pLASSO 载体支持方案 2:制备预 LASSO 基本方案 2:使用 LASSO 探针大规模并行捕获大 DNA。