- この都医学研セミナーは終了しました。-
演者 | 秋吉 文悟 Department of Biochemistry, University of Oxford, UK Group Leader |
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会場 | オンライン(Zoom) |
日時 | 2022年6月17日(金曜日)16:00~ |
世話人 | 宮岡 佑一郎 再生医療プロジェクトリーダー |
参加自由 | 詳細は下記問合せ先まで |
お問い合わせ |
研究推進課 普及広報係 電話 03-5316-3109 |
Biologists can learn a lot of lessons from exceptions. Although it was widely assumed that the macromolecular protein complex that drives chromosome segregation (called the kinetochore) consists of proteins that are common to all eukaryotes, no canonical kinetochore components have been identified in a group of organisms called kinetoplastids, which are evolutionarily divergent from yeast or human. To reveal how kinetoplastids achieve chromosome segregation, we identified 25 kinetochore proteins in Trypanosoma brucei (a kinetoplastid parasite that causes African sleeping sickness) and discovered that they constitute kinetochores that are specifically found in kinetoplastids. We are currently characterizing these “exceptional” kinetochore proteins in vitro and in vivo to understand how they carry out conserved kinetochore functions, such as binding to DNA and microtubules as well as error correction. By understanding how kinetoplastids segregate their chromosomes, we aim to understand fundamental principles of chromosome segregation machinery.