BSc (Nanjing University); PhD (Case Western Reserve University, USA)
Professor
Guoping Fan is currently a Full Professor at the School of Biomedical Sciences, The University of Hong Kong. He obtained a BSc degree in Biochemistry from Nanjing Univesity and a PhD in Neurosciences from Case Western Reserve University, USA. After completing postdoc training at the Whitehead Institute/MIT in 2001, he was appointed as a faculty member at the Department of Human Genetics, David Geffen School Medicine at University of California Los Angeles (UCLA). At UCLA, he rose to the rank of full Professor in 2011 and has become Professor Emeritus since 2021. From 2019 to 2024, Professor Fan was also appointed as a distinguished adjunct professor at the ShanghaiTech University, and subsequently became an adjunct professor Scintillon Research Institute in San Diego, California from 2024. He has published over 120 original papers, reviews and book chapter with citations >25,000. Professor Fan has served as a regular grant reviewer for many agencies including NIH, Maryland, Connecticut, and Pennsylvania States, several Europe countries and Natural Science Foundation of China. He was awarded as a Basil O’Connor Scholar, Carol Moss Spivak Scholar in Neuroscience, Royan International Research Award in Embryology, and a recipient of the First Prize Award in Science and Technology Award from Chinese Medical Society. Professor Fan has been a board member of Chinese Society of Stem Cell Research since 2021.
Our current research focuses on understanding epigenetic mechanisms that regulate neural stem cell differentiation, adult brain function, and somatic cell reprogramming. We utilize advanced molecular and genetic approaches to investigating how DNA cytosine methylation and its associated components, which include methyl-CpG binding proteins and histone modification enzymes, regulate gene expression, cell differentiation and reprogramming, and neural plasticity in mammalian systems.
DNA methylation in development and disease: Abnormal DNA methylation has been associated with several human neurological disorders, including fragile-X, ICF (immunodeficiency, centromere instability, and facial anomaly), and Tatton-Brown-Rahman Syndrome, human overgrowth and dwarfism syndromes. To study the methylation function in the brain, we have used the Cre/loxP conditional gene knockout method to produce transgenic mice that are deficient of the DNA methyltransferases (Dnmts) exclusively in the central nervous system (CNS). More recently, we have used CRSIPR-Cas technology to introduce point mutations in DNMTs to model human diseases in transgenic mice. Dnmt1 deficiency results in DNA hypomethylation in CNS precursor cells and their progeny neuronal and glial cells. We found that DNA hypomethylation affects neuronal and astroglial differentiation as well as postnatal neuronal survival and maturation in the CNS. We have developed human disease-specific iPSCs to dissect molecular and epigenetic mechanisms underlying these human diseases through directed cell lineage-specific differentiation and organoid development. Understanding epigenetic mechanisms underlying development and disease allows us to devise novel methods to effectively treat human disease through epigenetic gene modifications.
Last Update : 2025-12-10