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Molecular and Cellular Biology

Houston, Texas

Image 1: Ovulated mouse cumulus cell oocyte complex immunostained for matrix proteins hyaluronan and versican. By JoAnne Richards, Ph.D.; Image 2: By Yi LI, Ph.D.; Image 3: Mouse oocyte at meiosis I immunostained for tubulin (red) phosphop38MAPK (green) and DNA (blue). By JoAnne Richards, Ph.D.; Image 4: Expanded cumulus cell ooctye ocmplex immunostained for hyaluronan (red), TSG6 (green) and DAN (blue). By JoAnne Richards, Ph.D.; Image 5: Epithelial cells taken from a mouse mammary gland were cultured in a dish and transduced with a retrovirus expressing two genes. The green staining shows green fluorescent protein and the red staining shows progesterone receptor expression. The nucleus of each cell is stained blue. Photomicrograph taken at 200X magnification. By Sandra L. Grimm, Ph.D.; Image 6: Ovarian vasculature (red) is excluded from the granulosa cells (blue) within growing follicles (round structures); Image 7: Ovulated mouse cumulus cell oocyte complex immunostained for matrix proteins hyaluronan and versican. By JoAnne Richards, Ph.D.
Department of Molecular and Cellular Biology
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Soo-Kyung Lee, Ph.D.

Soo-Kyung Lee, Ph.D. photoAssistant Professor
Department of Molecular and Cellular Biology

Education

Ph.D.: Chonnam National University, Kwangju, Korea
Postdoctoral training: The Salk Institute, La Jolla

Research Interest

Transcriptional Regulatory Network in Developing Central Nervous System
Unravelling the processes that generate the numerous neuronal subtypes and establish their appropriate connections to form a functional CNS is one of the main challenges in neuroscience today. Particularly, decoding the transcriptional regulatory network responsible for neuronal subtype specification is a fundamental step toward understanding the CNS development and advancing methods to generate specific neurons in regenerative medicine.

Our goal is to develop a comprehensive map of the complex gene regulatory networks that direct cell-fate specification and assembly of neuro-circuits. Our major model systems include the spinal cord, which consists of distinct classes of neurons to assemble motor and sensory circuits, and the arcuate nucleus of the hypothalamus, which forms a core neuro-circuitry that mediates actions of peripheral adiposity-signals, leptin and insulin, for energy balance. To achieve our goals, we dissect multiple layers of gene regulatory steps that render neuronal cell-fate specification, taking the following steps; to define transcription complexes specifying each neuronal population, to identify their downstream effector genes conferring unique cell-identity, to understand epigenetic strategy orchestrating timely changes on gene transcription, to uncover the molecular mechanism by which the peripheral cues modulate neuronal gene expression, and to generate specific neuronal subtypes from stem cells by applying the developmental gene regulatory strategy that we define. Our study will eventually contribute to the design of a rational strategy to repair damaged neurons and to treat metabolic disorders in the human.

Having been pioneering combinatorial transcription code studies in the spinal cord development for the past years, we have developed many molecular tools and animal model systems that enable us to explore critical layers of transcriptional regulation, such as epigenetic control, and that are applicable to investigating other areas of the CNS. We are employing combined approaches of mouse genetics and chick embryology to take advantage of their complementary strengths as experimental systems. In addition, we are utilizing embryonic stem cells extensively and biochemical and molecular methods to dissect the development of spinal and hypothalamic neurons.
Lateral view of chick embryos showing GFP+ motor axon projections into the forelimb (FL). Inset shows the ventral spinal cord labeled by markers GFP and Lhx3 (red). Dotted arrows indicate the GFP+ axonal paths. SC, spinal cord. Lab slide.
Lateral view of chick embryos showing GFP+ motor axon projections into the forelimb (FL). Inset shows the ventral spinal cord labeled by markers GFP and Lhx3 (red). Dotted arrows indicate the GFP+ axonal paths. SC, spinal cord.

Contact Information

Baylor College of Medicine
One Baylor Plaza, Room S840
Mail Stop: BCM130
Houston, TX 77030

Phone: 713-798-8524
Fax: 713-798-8967
E-mail: sklee@bcm.edu

Lab website: http://www.bcm.edu/genetics/neurometatrans/

Selected Publications

  1. Lee S, Lee B, Lee JW, Lee SK (2009). Retinoid signaling and Ngn2 function are coupled for the specification of spinal motor neurons through a chromatin modifier CBP. Neuron, in press.
  2. Joshi K, Lee S, Lee B, Lee JW, Lee SK (2009). LMO4 as a key controller of the balance between excitatory and inhibitory V2 interneurons. Neuron 61: 839-851.
  3. Lee S, Lee B, Joshi K, Pfaff S, Lee JW, Lee SK (2008). A novel regulatory network to segregate spinal neuronal identities. Dev. Cell 14: 877-889.
  4. Visvanathan J, Lee S, Lee B, Lee JW, Lee SK (2007). The microRNA miR-124 antagonizes the anti-neural REST/SCP1 pathway during embryonic CNS development. Genes Dev. 21: 744-749.
  5. Yeo M*, Lee SK*, Lee B, Ruiz EC, Pfaff SL, Gill G (2005). SCP1 phosphatase functions in neuronal gene expression. Science 307: 596-600. (*equal contributors)
  6. Lee SK, Lee B, Ruiz EC, Pfaff SL (2005). Olig2 and Ngn2 function in opposition to modulate gene expression in motor neuron progenitor cells. Genes Dev. 19: 282-294.
  7. Lee SK, Pfaff SL (2003). Synchronization of neurogenesis and motor neuron specification by direct coupling of bHLH and homeodomain transcription factors. Neuron 38: 731-745. This article was accompanied by a separate preview by D.W. Allan and S. Thor (Neuron 38: 675-677, 2003).
  8. Thaler JP*, Lee SK*, Jurata LW*, Gill GN, Pfaff SL (2002). LIM factor Lhx3 contributes to the specification of motor neuron and interneuron identity through cell type-specific protein-protein interactions. Cell 110: 237-249. (*equal contributors)
  9. Lee SK, Pfaff SL (2001). Transcriptional networks regulating neuronal identity in the developing spinal cord. Nat. Neurosci. 4: 1183-1191. (review)

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