Updated on 2025/04/20

写真a

 
TOZAWA Sayo
 
Organization
Faculty of Science and Engineering Research Associate
Contact information
The inquiry by e-mail is 《here
External link

Degree

  • 博士(医科学) ( 鳥取大学 )

  • 修士(医科学) ( 鳥取大学 )

Education

  • 2025.3
     

    Tottori University   doctor course   completed

  • 2022.3
     

    Tottori University   master course   completed

  • 2020.3
     

    Tottori University   graduated

Research History

  • 2025.4 - Now

    Chuo University   Faculty of Science and Engineering Department of Biological Sciences   Assistant Professor

  • 2023.4 - 2025.3

    Japan Society for the Promotion of Science

Research Areas

  • Life Science / Developmental biology

Papers

  • Novel function of Hox13 in regulating outgrowth of the newt hindlimb bud through interaction with Fgf10 and Tbx4.

    Sayo Tozawa, Haruka Matsubara, Fumina Minamitani, Yasuhiro Kamei, Misako Saida, Momoko Asao, Ken-Ichi T Suzuki, Masatoshi Matsunami, Shuji Shigenobu, Toshinori Hayashi, Gembu Abe, Takashi Takeuchi

    Development, growth & differentiation   67 ( 1 )   10 - 22   2025.1

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    Language:English   Publishing type:Research paper (scientific journal)  

    5'Hox genes regulate pattern formation along the axes of the limb. Previously, we showed that Hoxa13/Hoxd13 double-mutant newts lacked all digits of the forelimbs during development and regeneration, showing that newt Hox13 is necessary for digit formation in development and regeneration. In addition, we found another unique phenotype. Some of the Hox13 crispant newts showed hindlimb defects, in which whole or almost whole hindlimbs were lost, suggesting a novel function of Hox13 in limb development. Using germline mutants, we showed that mutation in Hox13 led to hindlimb defects. The limb buds of Hox13 crispants formed, however, did not show outgrowth. Expression of Fgf10 and Tbx4, which are involved in limb outgrowth, decreased in the hindlimb buds of Hox13 crispants. In addition, hindlimb defects were observed in both Fgf10 and Tbx4 crispant newts. Finally, Fgf10 and Tbx4 interacted with Hox13 genetically. Our results revealed a novel function of Hox13 in regulating the outgrowth of the newt hindlimb bud through interaction with Fgf10 and Tbx4.

    DOI: 10.1111/dgd.12952

    PubMed

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  • Newt Hoxa13 has an essential and predominant role in digit formation during development and regeneration. International journal

    Takashi Takeuchi, Haruka Matsubara, Fumina Minamitani, Yukio Satoh, Sayo Tozawa, Tomoki Moriyama, Kohei Maruyama, Ken-Ichi T Suzuki, Shuji Shigenobu, Takeshi Inoue, Koji Tamura, Kiyokazu Agata, Toshinori Hayashi

    Development (Cambridge, England)   149 ( 5 )   2022.3

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    Language:English   Publishing type:Research paper (scientific journal)  

    The 5'Hox genes play crucial roles in limb development and specify regions in the proximal-distal axis of limbs. However, there is no direct genetic evidence that Hox genes are essential for limb development in non-mammalian tetrapods or for limb regeneration. Here, we produced single to quadruple Hox13 paralog mutants using the CRISPR/Cas9 system in newts (Pleurodeles waltl), which have strong regenerative capacities, and also produced germline mutants. We show that Hox13 genes are essential for digit formation in development, as in mice. In addition, Hoxa13 has a predominant role in digit formation, unlike in mice. The predominance is probably due to the restricted expression pattern of Hoxd13 in limb buds and the strong dependence of Hoxd13 expression on Hoxa13. Finally, we demonstrate that Hox13 genes are also necessary for digit formation in limb regeneration. Our findings reveal that the general function of Hox13 genes is conserved between limb development and regeneration, and across taxa. The predominance of Hoxa13 function both in newt limbs and fish fins, but not in mouse limbs, suggests a potential contribution of Hoxa13 function in fin-to-limb transition.

    DOI: 10.1242/dev.200282

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Research Projects

  • 肢発生におけるHox13遺伝子の機能を見直す

    Grant number:23KJ1596  2023.4 - 2025.3

    日本学術振興会  科学研究費助成事業  特別研究員奨励費  鳥取大学

    戸澤 紗代

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    Grant amount: \1800000 ( Direct Cost: \1800000 )

    Hox遺伝子群は、動物の発生における体の前後軸や四肢の遠近軸、前後軸のパターン形成を制御する。Hox13遺伝子はノックアウトマウスの研究から指の形成に必要であることが明らかにされた。しかし、マウスと異なり、イモリHox13遺伝子の変異体では、指形成の異常に加えて、一部の個体で後肢全体が欠損(以下、後肢欠損)した。他の四肢動物においてHox13の機能を探る遺伝学的な研究は行われておらず、この後肢欠損の解析はHox13の新たな機能の解明や四肢の発生機構の理解につながる。これまで、Hox13変異体の後肢欠損肢で後肢形成や肢芽伸長に必要な遺伝子(Fgf10, Tbx4等)の発現が低下することを明らかにした。この結果から、Hox13はFgf10, Tbx4等の発現を調節することで後肢が正常に伸長するという仮説を立てた。この仮説の検証には、2024年度の研究計画(Fgf10, Tbx4等の機能解析)がより重要であると判断し、2023年度に前倒しで実施した。そして、Fgf10およびTbx4の変異体をそれぞれ、作製したところ、いずれも、一部の個体でHox13変異体と同様に後肢欠損が生じた。次に、Fgf10, Tbx4変異体の後肢の骨形態を骨染色やマイクロCTで詳細に解析した。その結果、それぞれの変異体の一部の個体では、大腿骨を含め、それより遠位部の骨構造が全て欠損した。この表現型は、Hox13変異体のものと同様で、これらの結果は仮説を支持する。

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