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黃怡萱  教授    Yi-Shuian Huang, PhD

               ◼  Position/Affiliation/E-mail
               Position/Affiliation:

               Research  Fellow  &  Deputy  Director,  Institute  of  Biomedical  Sciences,
               Academia Sinica
               E-mail: yishuian@ibms.sinica.edu.tw


               ◼  Biography
                  Dr. Yi-Shuian Huang received a Ph.D. in Biochemistry and Molecular Biology from the
               University of Texas Southwestern Medical Center and currently serves as Research Fellow and
               Deputy Director at the Institute of Biomedical Sciences, Academia Sinica. Her research focuses

               on  the  molecular  basis  of  brain  development  and  memory,  particularly  how  experience-
               dependent synaptic plasticity is regulated by RNA-binding proteins and cap methyltransferases
               in the mammalian central nervous system.
                  A  central  theme  of  her  work  is  understanding  how  localized  translation  of  mRNAs  at

               synapses  supplies  plasticity-related  proteins  critical  for  long-term  memory.  Her  group  has
               studied  the  cytoplasmic  polyadenylation  element-binding  proteins  (CPEBs)  and  uncovered
               their roles in translation regulation, nucleocytoplasmic shuttling, and stress granule dynamics.
               These efforts have resulted in 25 peer-reviewed publications and an invited Expert Review in

               Molecular Psychiatry on “CPEB in Memory and Neurological Disorders.” Notably, her team
               provided  the  first  direct  evidence  that  axonal  translation,  mediated  by  CPEB2,  regulates
               glutamatergic transmission, presynaptic plasticity, and memory formation.
                  Building  on  these  findings,  her  current  research  investigates  RNA  epitranscriptomic

               regulation in brain development and memory. Specifically, her group examines the roles of cap
               methyltransferases CMTR1 and CMTR2. In parallel, two program projects are underway: one
               explores how tau mRNA 3′-UTR length influences its localization, translation, and function in
               synaptic  plasticity;  the  other  investigates  CADASIL  pathogenesis  using  mouse  models.

               Together, these studies aim to illuminate molecular pathways underlying neurodegenerative
               and cerebrovascular disorders, paving the way for new therapeutic strategies.


















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