Researcher Information

KOTANI Tomoya

Associate Professor

To unravel mysteries in the birth of animals

Department of Biological Sciences, Reproductive and Developmental Biology

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Theme

To elucidate cellular and mollecular mechanisms of vertebrate oogenesis and embryogenesis

FieldCell Biology, Molecular Biology, Developmental Biology, Genetics
KeywordZebrafish, Mouse, Maternal Factor, Oogeneis, Early Development, Insertional Mutation, Transposon, Meiosis, Mitotic Cleavage, Morphogenesis, Embryonic Axis Formation

Introduction of Research

A multicellular organism begins with a single cell, the fertilized egg. Although oogenesis and development of many species have been morphologically analyzed, little is known about physiological control of these processes. Maternal factors, which are accumulated in the egg during oogenesis, control almost all cellular functions and patterning decisions that occur prior to the activation of zygotic genome and further promote many processes beyond this period. Recent studies demonstrated that more than ten thousand mRNAs are accumulated in vertebrate oocytes. Interestingly, thousands of them are translationally repressed in the egg and are activated at the appropriate time and site after fertilization, promoting the progression of diverse developmental processes. We investigated maternal factors deposited in oocytes that promote developmental processes using zebrafish and mice as model animals. Our aim is to find previously unknown principles that drive developmental processes by isolating and analyzing maternal factors.

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Maternal factors and vertebrate development
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Screening for maternal factors by a gene trap method
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mRNA forming granules in the oocyte cytoplasm

Representative Achievements

Alternative 3′ UTRs and RNA-binding proteins Ewsr1b, HuR, and Syncrip organize sequential waves of translation to drive embryonic development. K. Sato, L. Fierro, A. Suginishi, T. Sanada, T. Kotani. Cell Reports, 2026, vol.45, 117557.
Mature mRNA processing that deletes 3’ end sequences directs translational activation and embryonic development. Y. Takada, L. Fierro, K. Sato, T. Sanada, A. Ishii, T. Yamamoto, T. Kotani. Science Advances, 2023, vol.9, eadg6532.
Identification of embryonic RNA granules that act as sites of mRNA translation after changing their physical properties. K. Sato, M. Sakai, A. Ishii, K. Maehata, Y. Takada, K. Yasuda, T. Kotani. iScience, 2022, vol.25, 104344.
Tdrd3 regulates the progression of meiosis II through translational control of Emi2 mRNA in mouse oocytes. N. Takei, K. Sato, Y. Takada, R. Lyyappan, A. Susor, T. Yamamoto, T. Kotani. Current Research in Cell Biology, 2021, vol.2, 100009.
Changes in subcellular structures and states of pumilio1 regulate the translation of target Mad2 and cyclin B1 mRNAs. N. Takei, Y. Takada, S. Kawamura, K. Sato, A. Saitoh, J. Bormann, WS. Yuen, J. Carroll, T. Kotani. Journal of Cell Science, 2020, vol.133, jcs249128.
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Academic degreePh.D.