J. Craig Venter Institute, 4120 Capricorn Lane, La Jolla, CA 92037, USA.
Codex DNA, 9535 Waples St #100, San Diego, CA 92121, USA.
Int J Mol Sci. 2020 Sep 26;21(19):7112. doi: 10.3390/ijms21197112.
() is an increasingly popular industrially relevant yeast. It is known to possess a highly efficient non-homologous end joining (NHEJ) pathway that promotes random integration of non-homologous DNA fragments into its genome. The nature of the integration events was traditionally analyzed by Southern blot hybridization. However, the precise DNA sequence at the insertion sites were not fully explored. We transformed a PCR product of the gene () into an uracil auxotroph otherwise wildtype strain and picked 24 stable Ura+ transformants for sequencing analysis. We took advantage of rapid advances in DNA sequencing technologies and developed a method using a combination of Illumina MiSeq and Oxford Nanopore sequencing. This approach enables us to uncover the gross chromosomal rearrangements (GCRs) that are associated with the random integration. Moreover, it will shine a light on understanding DNA repair mechanisms in eukaryotes, which could potentially provide insights for cancer research.
()是一种日益流行的具有工业相关性的酵母。已知它具有高效的非同源末端连接(NHEJ)途径,可促进非同源 DNA 片段随机整合到其基因组中。传统上通过 Southern 印迹杂交分析整合事件的性质。然而,插入位点的精确 DNA 序列并未得到充分探索。我们将基因()的 PCR 产物转化为尿嘧啶营养缺陷型(ura)菌株,否则为野生型菌株,并对 24 个稳定的 Ura+转化体进行测序分析。我们利用 DNA 测序技术的快速发展,开发了一种结合使用 Illumina MiSeq 和 Oxford Nanopore 测序的方法。这种方法使我们能够揭示与随机整合相关的大染色体重排(GCR)。此外,它将有助于了解真核生物中的 DNA 修复机制,这可能为癌症研究提供启示。