Soo-Kyung Lee

PhD

Soo Lee.

Soo-Kyung Lee

PhD

Soo-Kyung Lee

PhD

Empire Innovation Professor
Om P. Bahl Endowed Professor

Research Interests

Development of neurons and glial cells, neurodevelopmental disorders

Contact Information

C533 Cooke Hall

Buffalo NY, 14260

Phone: (716) 645-4996

slee229@buffalo.edu

Education

  • PhD, Chonnam National University, Korea

Research Summary

We are recruiting postdocs as well as undergraduate and graduate students. 

 

 

Soo-Kyung Lee’s long-term goals are to dissect gene regulatory events that lead to the cellular diversity and eventually formation of functional neural circuits in the CNS and to understand genetic and mechanistic basis for neurodevelopmental defects, ultimately contributing to the generation of better treatment strategies for human developmental disorders. 

Over the past decade, Lee has pioneered biochemical and molecular approaches in mouse and chick embryos to unravel the fundamental principles controlling gene expression and cell fate specification in the developing CNS. This led to a series of seminal discoveries into the gene regulatory network required for neuronal fate specification.

More recently, Lee has begun dissecting a human autism disorder FoxG1 syndrome, characterized by severe deficits in cortex development along with other life-threatening symptoms. Soo is devoted to understanding the FoxG1 biology and also engaged in translational research to find a cure for the disorder. 

Selected Publications

  • F. Cargnin, J.S.Kwon, S.Katzman, B.Chen, J.W.Lee and S.-K.Lee. FOXG1 orchestartes neocortical organization and cortico-cortical connections. Neuron100, 1083-1096, 2018.
  • Y. Colvis, J.-S.Kwon, S.Y.Seo, J.C.Rhee, S.Yeo, J.W.Lee, S.Lee and S.-K.Lee. Chx10 consolidates V2a interneuron identity through two distinct gene repression modes. Cell Reports16, 1642-52,2016.
  • K.P. Thiebes, H.Nam, X.A.Cambronne, R.Shen, S.M.Glasgow, H.H.Cho, J.Kwon, R.H.Goodman, J.W.Lee, S.Lee*and S.-K.Lee*.(*co-corresponding authors) miR-218 is essential to establish motor neuron fate as a downstream effector of Isl1-Lhx3. Nature Communications6, 7718, 2015.
  • H.H.Cho, R.Shen, A.P.Barnes, J.W.Lee, S.Lee, and S.-K.Lee. Isl1 directly controls a cholinergic neuronal identity by forming cell type-specific complexes in the developing forebrain and spinal cord.PLOS GeneticsDOI: 10.1371/journal.pgen. 1004280, 2014.
  • S. Lee, J.W.Lee, and S.-K.Lee. UTX, a histone H3-lysine 27 demethylase, acts as a critical switch to activate the cardiac developmental program. Developmental Cell, 22, 25-37, 2012. 
  • K. Joshi, S.Lee, B.Lee, J.W.Lee, and S.-K.Lee. LMO4 controls of the balance between excitatory and inhibitory V2-interneurons.Neuron,61, 839-51, 2009.
  • S. Lee, B.Lee, J.W.Lee, and S.-K.Lee. Retinoid signaling and Neurogenin2 function are coupled for the specification of spinal motor neurons through a chromatin modifier CBP. Neuron,62:641-54, 2009. 
  • S. Lee, B. Lee, K. Joshi, S. Pfaff, J.W.Lee, and S.-K.Lee. A regulatory network to segregate spinal neuronal subtypes. Developmental Cell,14: 877-89, 2008.