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公开(公告)号:US20220186263A1
公开(公告)日:2022-06-16
申请号:US17601303
申请日:2020-04-03
Applicant: OSAKA UNIVERSITY
Inventor: Tomoji MASHIMO , Kazuto YOSHIMI , Yoshihiro UNO , Yuko KOTANI , Yoshiki MIYASAKA , Yuichiro OKA , Makoto SATO
Abstract: The present inventors have found that the use of a site-specific nuclease system which includes a combination of a molecule that simultaneously targets and cleaves one homology arm sequence of the donor DNA and the genomic sequence corresponding to the homology arm sequence, and a molecule that targets and cleaves the genomic region in the vicinity of the cleavage site by that molecule causes repair between genomic DNA and donor DNA through both non-homologous end joining and homologous recombination, making it possible to produce cells and organisms with knocked-in long donor sequences with high efficiency and accuracy.
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公开(公告)号:US20240124898A1
公开(公告)日:2024-04-18
申请号:US18467297
申请日:2023-09-14
Applicant: OSAKA UNIVERSITY
Inventor: Tomoji MASHIMO , Junji TAKEDA , Hiroyuki MORISAKA , Kazuto YOSHIMI
CPC classification number: C12N15/907 , A61K48/00 , C12N5/14 , C12N5/16 , C12N9/22 , C12N15/85 , C12N15/8509 , C12N2310/20 , C12N2800/22 , C12N2800/80
Abstract: A CRISPR-Cas3 system was successfully established in a eukaryotic cell.
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公开(公告)号:US20230099483A1
公开(公告)日:2023-03-30
申请号:US17794704
申请日:2021-01-25
Applicant: C4U CORPORATION , OSAKA UNIVERSITY
Inventor: Tomoji MASHIMO , Kazuto YOSHIMI , Satomi SHIBUMURA
IPC: C12Q1/70
Abstract: It has been found that by mixing a single-stranded probe DNA whose cleavage can be detected in a reaction system containing a CRISPR-Cas3 system and a sample from which to detect a target DNA, it is possible to detect the target DNA in the sample by using, as indication, a signal generated by the cleavage of the single-stranded probe DNA.
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公开(公告)号:US20200029538A1
公开(公告)日:2020-01-30
申请号:US16463883
申请日:2017-11-24
Applicant: OSAKA UNIVERSITY
Inventor: Tomoji MASHIMO , Yoshiki MIYASAKA
IPC: A01K67/027 , C12N15/90 , C12N15/10
Abstract: A method for producing a genome edited cell or a non-human organism, comprising the step of introducing (a) an artificial nuclease system which cleaves both ends of a genome editing target region, and (b) a nucleic acid sequence formed by arranging a 5′-side homology arm sequence, a donor DNA sequence, and a 3′-side homology arm sequence in this order from a 5′-side, the 5′-side homology arm sequence being a homologous sequence of one nucleic acid sequence outside the genome editing target region, and the 3′-side homology arm sequence being a homologous sequence of the other nucleic acid sequence outside the genome editing target region, into a cell or a non-human organism.
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公开(公告)号:US20240117381A1
公开(公告)日:2024-04-11
申请号:US18467356
申请日:2023-09-14
Applicant: OSAKA UNIVERSITY
Inventor: Tomoji MASHIMO , Junji TAKEDA , Hiroyuki MORISAKA , Kazuto YOSHIMI
CPC classification number: C12N15/907 , A61K48/00 , C12N5/14 , C12N5/16 , C12N9/22 , C12N15/85 , C12N15/8509 , C12N2310/20 , C12N2800/22 , C12N2800/80
Abstract: A CRISPR-Cas3 system was successfully established in a eukaryotic cell.
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公开(公告)号:US20220017888A1
公开(公告)日:2022-01-20
申请号:US17309607
申请日:2019-12-11
Applicant: Kyoto University , Osaka University
Inventor: Akitsu HOTTA , Yuya OKUZAKI , Huaigeng XU , Peter David GEE , Yuto KITA , Tomoji MASHIMO , Kazuto YOSHIMI
Abstract: A production method of genomic DNA in which a deletion of more than 100 bases of nucleotides is introduced into a target region of the genomic DNA, the method includes a contact step of bringing a type I CRISPR associated complex for anti-viral defense (type I Cascade complex), CRISPR RNA (crRNA), and Cas3 protein into contact with the genomic DNA.
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