| Literature DB >> 27780671 |
Osamu Mizutani1, Takayuki Arazoe2, Kenji Toshida3, Risa Hayashi3, Shuichi Ohsato2, Tetsushi Sakuma4, Takashi Yamamoto4, Shigeru Kuwata2, Osamu Yamada3.
Abstract
Transcription activator-like effector nucleases (TALENs), which can generate DNA double-strand breaks at specific sites in the desired genome locus, have been used in many organisms as a tool for genome editing. In Aspergilli, including Aspergillus oryzae, however, the use of TALENs has not been validated. In this study, we performed genome editing of A. oryzae wild-type strain via error of nonhomologous end-joining (NHEJ) repair by transient expression of high-efficiency Platinum-Fungal TALENs (PtFg TALENs). Targeted mutations were observed as various mutation patterns. In particular, approximately half of the PtFg TALEN-mediated deletion mutants had deletions larger than 1 kb in the TALEN-targeting region. We also conducted PtFg TALEN-based genome editing in A. oryzae ligD disruptant (ΔligD) lacking the ligD gene involved in the final step of the NHEJ repair and found that mutations were still obtained as well as wild-type. In this case, the ratio of the large deletions reduced compared to PtFg TALEN-based genome editing in the wild-type. In conclusion, we demonstrate that PtFg TALENs are sufficiently functional to cause genome editing via error of NHEJ in A. oryzae. In addition, we reveal that genome editing using TALENs in A. oryzae tends to cause large deletions at the target region, which were partly suppressed by deletion of ligD.Entities:
Keywords: Aspergillus oryzae; Genome editing; Large deletion; Nonhomologous end-joining; Transcription activator-like effector nucleases; ligD
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Year: 2016 PMID: 27780671 DOI: 10.1016/j.jbiosc.2016.09.014
Source DB: PubMed Journal: J Biosci Bioeng ISSN: 1347-4421 Impact factor: 2.894