Kotaro Fujii

Kotaro Fujii, PhD

Kotaro Fujii, Ph.D.
Assistant Professor of UF MGM


University of Florida
Dept. of Molecular Genetics & Microbiology
2033 Mowry Rd.
Gainesville, FL. 32610



Research in the Fujii lab

Dr. Fujii’s research is centered on understanding of the gene regulation focusing on the step of mRNA translation. Our research program will unravel new layers of spatiotemporal specificity and fidelity of protein synthesis, to further understand the impact of translational regulation in development and in diseases, particularly those caused by protein aggregation such as neurodegenerative disorders.

RNA Translation

How to build up functional proteome?

A key factor in ensuring human health and longevity is the homeostasis of proteins, which are the building blocks of our bodies and maintain cell type specific functions. Indeed, loss of proteostasis is a hallmark of aging and neurological diseases. To maintain functional protein synthesis, eukaryotic cells have a quality control system eliminating non-functional ribosomes that can not produce protein [Fujii et al. Genes Dev 2009, EMBO.J 2012]. However, the protein production step, mRNA translation, is highly error-prone to amino acid misincorporation, stop codon readthrough, and ribosomal frameshifting. By focusing on the ribosome, we found a molecular mechanism to increase accuracy of ribosomal decoding in eukaryotes beyond prokaryotes [Fujii et al. Mol Cell 2018]. We further seek to understand the dynamics of such regulation in mammalian organisms and how regulation contributes to our health.

Key questions:

  • What are the dynamics of translation fidelity between tissues during mammalian development, across aging, and in disease?
  • What is the molecular mechanism that regulates the accuracy of ribosomal decoding?
  • How can we make ribosomes that do not synthesize trash?

Decoding the role of mRNA translation in cell signaling

A key factor for the spatiotemporal queue in developing embryos is developmental cell signaling which allows each cell to “know” where they are and what to become. However, all cell signaling has been used multiple times during embryonic development in different contexts and how signaling is specialized for each specific context is still not well understood. Although mRNA translation has been thought as always “on” state, we found that translation of important developmental signaling circuitry including Shh, Wnt, and Hippo signaling are highly repressed and differentially regulated between tissues [Fujii et al. Nat Commun 2017]. We want to mechanistically understand how translational regulation of signaling transcripts impacts on tissue-specific signaling and species-specific tissue patterning.

Key questions:

  • What are the Cis-regulatory elements and trans-acting factors that regulate the translation of signaling transcripts?
  • What is the trigger to turn “on” the translation of signaling transcripts?
  • What is the impact of translation regulation on cell signaling for tissue specific signaling and species-specific tissue patterning?

Approach, Molecular Mechanism, Significance

We approach these outstanding questions using a variety of model systems such as mouse, culture cell, and yeast and apply state-of-the-art Biochemistry, Genetics, and Genomics to molecularly decode the impact of translation regulation in mammalian development and homeostasis.

Key publications

Fujii, K., Susanto, TT., Saurabh, S., and Barna, M. Decoding the function of expansion segments in ribosomes. Molecular Cell 72, 1013-1020 (2018) DOI: 10.1016/j.molcel.2018.11.023

Shi, Z., *Fujii, K., Kovary, K.M., Genuth, N.R., Röst, H.L., Teruel, M.N., and Barna, M. Heterogeneous ribosomes preferentially translate distinct subpools of mRNAs genome-wide. Molecular Cell 67, 71-83 (2017) co-first author DOI: 10.1016/j.molcel.2017.05.021

Fujii, K., Shi, Z., Zhulyn, O., Denans, N., and Barna, M. Pervasive translational regulation of the cell signaling circuitry underlies mammalian development. Nature Communications 8, 14443 (2017) co-first author DOI: 10.1038/ncomms14443

Fujii, K., Kitabatake, M., Sakata, T., and Ohno, M. 40S subunit dissociation and proteasome-dependent RNA degradation in non-functional 25S rRNA decay. The EMBO Journal 31, 2579-2589 (2012) co-first author DOI: 10.1038/emboj.2012.85

Fujii, K., Kitabatake, M., Sakata, T., Miyata, A., and Ohno, M. A role for ubiquitin in the clearance of nonfunctional rRNAs. Genes & Development 23, 963-974 (2009) co-first author DOI: 10.1101/gad.1775609