Dragony Fu
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Associate Professor
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About
Dragony Fu is an Associate Professor at the University of Rochester in the United States. His research focuses on tRNA modifications and their implications in neurological disorders, as evidenced by his recent publications on tRNA methyltransferases and adenosine deaminases. He employs innovative tools to investigate and analyze RNA modifications that play critical roles in neurodevelopment and synaptic function.
Recent Grants
Grant: Close
Molecular functions of the TRMT1 tRNA modification enzyme
Open Date: 2021-06-01
Close Date: 2025-03-31
Grant: Close
RAPID: Impact of SARS-CoV2 on function of the cellular tRNA methyltransferase 1 and redox homeostasis
Open Date: 2020-06-01
Close Date: 2021-05-31
Grant: Close
Function of TRM9L and tRNA wobble uridine modification in the nervous system
Open Date: 2020-03-01
Close Date: 2025-02-28
Grant: Close
CAREER: Elucidating the Targets and Functions of Mammalian tRNA methyltransferase orthologs
Open Date: 2015-12-01
Close Date: 2020-11-30
Grant: Close
SIRT1, Acidosis & Metabolism in Cardioprotection
Open Date: 2002-07-01
Close Date: 2020-06-30
Articles (10)
Nervous system function rests on the formation of functional synapses between neurons. We have identified TRMT9B as a new regulator of synapse formation and function in Drosophila . TRMT9B has been studied for its role as a tumor suppressor and is one of two metazoan homologs of yeast tRNA methyltransferase 9 (Trm9), which methylates tRNA wobble uridines. Whereas Trm9 homolog ALKBH8 is ubiquitously expressed, TRMT9B is enriched in the nervous system. However, in the absence of animal models, TRMT9B's role in the nervous system has remained unstudied. Here, we generate null alleles of TRMT9B and find it acts postsynaptically to regulate synaptogenesis and promote neurotransmission. Through liquid chromatography‐mass spectrometry, we find that ALKBH8 catalyzes canonical tRNA wobble uridine methylation, raising the question of whether TRMT9B is a methyltransferase. Structural modeling studies suggest TRMT9B retains methyltransferase function and, in vivo , disruption of key methyltransferase residues blocks TRMT9B's ability to rescue synaptic overgrowth, but not neurotransmitter release. These findings reveal distinct roles for TRMT9B in the nervous system and highlight the significance of tRNA methyltransferase family diversification in metazoans.
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2023
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2023
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2022
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2022
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2021
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2021
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2020
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2020
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2020
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2020
Collaborators (5)
Almundher Al‐Maawali
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Paul S. Brookes
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Stefanie M. Kaiser
Ludwig-Maximilians-Universität München
Kate M O'Connor‐Giles
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Christopher Prevost
University of Rochester
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