大学院薬学研究院

山崎 真巳

ヤマザキ マミ  (Mami Yamazaki)

基本情報

所属
千葉大学 大学院薬学研究院 教授
学位
薬学博士(1991年3月 千葉大学)

J-GLOBAL ID
200901084108778277
researchmap会員ID
1000191974

外部リンク

植物の化学多様性の分子基盤、進化に興味があります。

主要な論文

 172
  • Amit Rai, Hideki Hirakawa, Ryo Nakabayashi, Shinji Kikuchi, Koki Hayashi, Megha Rai, Hiroshi Tsugawa, Taiki Nakaya, Tetsuya Mori, Hideki Nagasaki, Runa Fukushi, Yoko Kusuya, Hiroki Takahashi, Hiroshi Uchiyama, Atsushi Toyoda, Shoko Hikosaka, Eiji Goto, Kazuki Saito, Mami Yamazaki
    Nature communications 12(1) 405-405 2021年1月15日  査読有り最終著者責任著者
    Plant genomes remain highly fragmented and are often characterized by hundreds to thousands of assembly gaps. Here, we report chromosome-level reference and phased genome assembly of Ophiorrhiza pumila, a camptothecin-producing medicinal plant, through an ordered multi-scaffolding and experimental validation approach. With 21 assembly gaps and a contig N50 of 18.49 Mb, Ophiorrhiza genome is one of the most complete plant genomes assembled to date. We also report 273 nitrogen-containing metabolites, including diverse monoterpene indole alkaloids (MIAs). A comparative genomics approach identifies strictosidine biogenesis as the origin of MIA evolution. The emergence of strictosidine biosynthesis-catalyzing enzymes precede downstream enzymes' evolution post γ whole-genome triplication, which occurred approximately 110 Mya in O. pumila, and before the whole-genome duplication in Camptotheca acuminata identified here. Combining comparative genome analysis, multi-omics analysis, and metabolic gene-cluster analysis, we propose a working model for MIA evolution, and a pangenome for MIA biosynthesis, which will help in establishing a sustainable supply of camptothecin.

MISC

 95

書籍等出版物

 17

講演・口頭発表等

 171

担当経験のある科目(授業)

 9

共同研究・競争的資金等の研究課題

 36

産業財産権

 4

社会貢献活動

 2