プログラム...14:30–15:00 Greg Gocal1, Christian Schöpke1, Mark Knuth1, Dave Songstad1, Steve Sanders1, Noel Sauer1, Peter Beetham1 (1Cibus, 6455 Nancy Ridge Dr., San Diego,
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
拡張型心筋症遺伝子変異に対する相同組換え修復(HDR)を介したゲノム編集治療の開発 / Genome editing via Homology-directed Repair targeting the mutation of dilated cardiomyopathy in cardiomyocytes
非典型的な homology directed repairによりDNA2本鎖切断を起こさずにゲノム編集が可能である / Genome Editing by Single Nicks in Target Gene and Donor Plasmid Enable Precise and Efficient Nucleotide Substitution through Non-Canonical Homology-Directed Repair
翻訳エンハンサー dMac3を利用したゲノム編集ツールによる低アミロースジャガイモの作出 / Improvement of the genome-editing tool, and creation of a low-amylose-starch potato, by applying the translational enhancer dMac3
ゲノム編集技術が社会に与えるインパクト / Impact of genome editing technologies on society
15:40–16:12 ○木下 政人 1(1京都大学 農学研究科)
ゲノム編集技術の水産業への応用の可能性
16:12–16:24 ○佐久間 哲史 1(1広島大・院理学)
ゲノム編集の技術開発と培養細胞での利用 / Development of genome editing technology and its application in cultured cells
16:24–16:36 ○刑部 祐里子 1,2(1徳島大・生物資源産業, 2理研・RInC)
植物のゲノム編集と農作物への応用
16:36–16:48 ○成瀬 清 1(1基礎生物学研究所 IBBPセンター)
生物遺伝資源のバックアップ拠点形成と新規凍結保存技術の開発 / Interuniversity Bio-Backup Project (IBBP) and the Collaborative Research Program for Development of New Cryopreservation Methods and Cryobiological Researches
16:48–17:00 ○八代 嘉美 1(1京都大学 iPS細胞研究所)
ゲノム編集と社会との関係について / Relationship between Genome Editing and Society
10:15–10:30
10:45–11:15
11:15–11:30
11:30–11:45
10 日本ゲノム編集学会 第 2回大会
Genome Editing English Session 発表日 6月30日(金) 13:00–15:30 会場 ライフホール
13:00–13:30 ○Benjamin P. Kleinstiver1-4, Alexander A. Sousa1-3, Moira M. Welch1-3, Michelle S. Prew1-3, Shengdar Q. Tsai1-4, Nhu T. Nguyen1-3, Vikram Pattanayak1-4, J. Keith Joung1-4 (1Molecular Pathology Unit, 2Center for Cancer Research, and 3Center for Computational and Integrative Biology,
MGH, Charlestown, MA 02129 USA, 4Department of Pathology, Harvard Medical School, Boston, MA 02115 USA)
Activities and Genome-wide Specificities of Engineered CRISPR Nucleases
13:30–14:00 ○Keiichiro Suzuki1, Yuji Tsunekawa2, Reyna Hernandez-Benitez1, Jun Wu1, Mako Yamamoto1, Fumio Matsuzaki2, Juan Carlos Izpisua Belmonte1 (1Gene Expression
Laboratory, Salk Institute for Biological Studies, 10010 N. Torrey Pines Rd., La Jolla, CA 92037, USA, 2Laboratory for Cell Asymmetry, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-Minamimachi,
Chuo-ku, Kobe 650-0047, Japan)
In vivo genome editing via CRISPR-Cas9 mediated homology-independent targeted integration
14:00–14:30 Chris Vakulskas1, Michael Collingwood1, ○Mark Behlke1 (1Integrated DNA Technologies)
High fidelity genome editing using RNP complexes with a novel mutant HiFi Cas9
Cross-ministerial Strategic Innovation Promotion Program(SIP), Technologies for Creating Next-Generation Agriculture, Forestry and Fisheries “Establishment of New Breeding Techniques”
14:30–15:00 ○Greg Gocal1, Christian Schöpke1, Mark Knuth1, Dave Songstad1, Steve Sanders1, Noel Sauer1, Peter Beetham1 (1Cibus, 6455 Nancy Ridge Dr., San Diego, CA 92129)
Precision Gene Editing in Agriculture.
15:00–15:30 ○Keiji Nishida1 (1Graduate School of Science, technology and Innovation, Kobe University)
Deaminase-mediated targeted nucleotide substitution and its applications
パネルディスカッション
倫理・規制セッション 発表日 6月30日(金) 15:45–17:00 会場 ライフホール
モデレーター:堀田秋津(京都大学)
ゲノム編集生物をどのように取り扱うか?~倫理および社会受容の観点から~ / How to deal with genome edited organisms? ̶from ethical and social acceptance point of views
ヒト培養細胞におけるCRISPR-ObLiGaRe法を用いた放射線発がんリスクの個人差を規定する遺伝素因の探索 / Screening of the genetic factors underlying individual differences of radiation-induced carcinogenesis using CRISPR-ObLiGaRe method in human cultured cells
ゲノム編集を用いた球脊髄性筋萎縮症(SBMA)の骨格筋病態の解明 / Pathophysiological analysis of skeletal muscles in spinal bulbar muscular atrophy (SBMA) by genome editing of CAG repeats
初期化過程におけるCRISPRを用いたKLF4 発現量依存的に誘導される上皮系遺伝子の機能 / CRISPR-based functional analysis of epithelial genes driven by high KLF4 stoichiometry in somatic cell reprogramming
拡張型心筋症遺伝子変異に対する相同組換え修復(HDR)を介したゲノム編集治療の開発 / Genome editing via Homology-directed Repair targeting the mutation of dilated cardiomyopathy in cardiomyocytes
Cas9タンパク /sgRNA複合体は編集箇所の再切断を抑え点変異導入効率を上昇させる / Cas9/gRNA ribonucleoprotein improved the efficiencies in single base mutation by reducing the re-cutting.
Cas9 RNP導入細胞のクローン化に伴うheterogeneityの解析 / Analysis of heterogeneity derived from Cas9 ribonucleoprotein-introduced clonal cells
P20 ○Masato Yonezawa1, Adam Blattler1, Hodaka Fujii2, Toshitsugu Fujita2, Brian Egan1, Terry Kelly1 (1Active Motif, Inc., Carlsbad, CA, USA, 2Chromatin Biochemistry Research Group, Research
Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan, Present affiliation: Dept. Biochem.
Genome Biol., Hirosaki University Grad. Sch. of Med.)
enChIP-Seq法による単一ゲノム領域の染色体ループ構造解析 / Identification of Chromosomal Looping Events at a Single Genomic Locus by enChIP-Seq
プラチナ TALE人工転写因子ならびにmultiplex SAMシステムを用いたCDH1遺伝子の発現誘導 / Transcriptional activation of CDH1 gene using the Platinum TALE-activator and the multiplex SAM system
非典型的な homology directed repairによりDNA2本鎖切断を起こさずにゲノム編集が可能である / Genome Editing by Single Nicks in Target Gene and Donor Plasmid Enable Precise and Efficient Nucleotide Substitution through Non-Canonical Homology-Directed Repair
PITCh法によるノックインの過程で生じるDSB修復経路の選択とその正確性 / Choice of DSB repair pathway and its accuracy during the process of PITCh knock-in
P31 ○Moe Hirosawa1,2, Yoshihiko Fujita1, Callum Parr1, Karin Hayashi1, Shunnichi Kashida1, Akitsu Hotta1, Knut Woltjen1,3, Hirohide Saito1 (1Department of Life Science Frontiers, Center for
iPS Cell Research and Application, Kyoto University, 2Graduate School of Medicine, Kyoto University, 3Hakubi
Center for Advanced Research, Kyoto University)
CRISPR-Cas9 systemによる細胞種特異的ゲノム編集 / Cell-type-specific genome editing with a microRNA-responsive CRISPR-Cas9 switch
オオミジンコにおけるCas9タンパク質を用いた高効率な遺伝子破壊法と遺伝子導入法の開発 / Highly efficient knock-out and non-homologous end joining-mediated knock-in by Cas9 protein injection in Daphnia magna
TALENを利用した非相同末端結合によるオオミジンコゲノムへのエストロゲンバイオセンサーの導入 / TALEN-mediated knock-in of an estrogen biosensor into Daphnia magna genome via non-homologous end joining
ネッタイツメガエルにおける sgRNA/Cas9タンパク質複合体を用いた高効率な遺伝子ノックアウト技術の確立 / Establishment of an efficient gene knock-out using Cas9 ribonucleoprotein complexes in Xenopus tropicalis founder
P42 ○重田 美津紀 1,山本 卓 1,鈴木 賢一 1(1広島大・院理学)
CRISPR-Cas9を用いたネッタイツメガエルの変態におけるオートファジー関連遺伝子の機能解析 / Functional analysis of autophagy related genes in Xenopus tropicalis metamorphosis using CRISPR-Cas9
16 日本ゲノム編集学会 第 2回大会
P43(O05) ○大石 勲 1(1産業技術総合研究所)
始原生殖細胞を用いたニワトリゲノム編集 / Chicken genome editing using primordial germ cells.
ゲノム編集技術を用いた鳥類性決定機構の解析 / Elucidation of mechanism of avian sex determination using genome editing
P45 ○金谷 哲平 1,江川 遼 1,八尾 寛 1(1東北大学 生命科学研究科 脳機能解析分野)
CRIPR/Cas9を用いた標識細胞特異的ノックアウト ― ニワトリ胚への応用と発達期ニューロンの分枝形態解析 / Genome editing of the fluorescence-labeled cells: Molecular mechanisms of axonal arborization during development of neurons in the chick embryo
CRISPR-Casシステムを用いたノックインマウス作製における凍結受精卵培養時間の検討 / Culture time of vitrified/warmed zygote before microinjection affects the production efficiency of CRISPR-Cas9-mediated knock-in mice
Team, RIKEN CLST, 2Animal Resource Development Unit, RIKEN CLST)
CRISPR/Cas9を用いた受精卵における遺伝子改変マウスの作製(神戸 RIKEN, LARGE) / Optimizing the one-step generation of genetically engineered mice with CRISPR/Cas9 in zygotes @ LARGE, RIKEN-Kobe
P55 ○Kenichi Nagata1, Mika Takahashi1, Takaomi Saido C.1 (1Laboratory for Proteolytic Neuroscience,
RIKEN Brain Science Institute)
CRISPR/Cas9システムによるDINE floxマウスの作製 / Generation of DINE-flox mice using CRISPR/Cas9 system
ゲノム編集を用いたモミラクトン生合成遺伝子の cis因子破壊によるクラスター転写制御への影響 / Effect of disruption of a cis-region on the coordinated expression of the momilactones biosynthetic genes cluster
翻訳エンハンサー dMac3を利用したゲノム編集ツールによる低アミロースジャガイモの作出 / Improvement of the genome-editing tool, and creation of a low-amylose-starch potato, by applying the translational enhancer dMac3