Seoul National University · 神経科学
Professor Yong-Seok Lee's research lab focuses on the neural and molecular mechanisms underlying learning, memory, and social behavior, with a particular emphasis on the prefrontal cortex and its subcortical circuits. The lab investigates how early-life experiences, such as social isolation, alter neuronal excitability and synaptic plasticity through conserved signaling pathways like cAMP/CREB and RAS/ERK. Using a combination of behavioral assays, chemogenetics, viral tracing, and molecular techniques in rodent and invertebrate models (e.g., Aplysia and C. elegans), the lab explores the genetic and cellular basis of neuropsychiatric disorders, including RASopathies. A central theme is the identification and functional characterization of G protein-coupled receptors and their roles in modulating neural circuits and long-term synaptic changes.
Figures are computed from collected data and may differ slightly.
Although medial prefrontal cortex (mPFC) is known to play important roles in social behaviors, how early social experiences affect the mPFC and its subcortical circuit remains unclear. We report that mice singly housed (SH) for 8 weeks after weaning show a social recognition deficit, even after 4 weeks of resocialization. In SH mice, prefrontal infralimbic (IL) neurons projecting to the shell region of nucleus accumbens (NAcSh) show decreased excitability compared with group-housed (GH) mice. NA
Whereas the induction of short-term memory involves only covalent modifications of constitutively expressed preexisting proteins, the formation of long-term memory requires gene expression, new RNA, and new protein synthesis. On the cellular level, transcriptional regulation is thought to be the starting point for a series of molecular steps necessary for both the initiation and maintenance of long-term synaptic facilitation (LTF). The core molecular features of transcriptional regulation involv
We have previously identified two G protein-linked acetylcholine receptors (GARs), GAR-1 and GAR-3, in the nematode Caenorhabditis elegans. Whereas GAR-3 is a homologue of muscarinic acetylcholine receptors (mAChRs), GAR-1 is similar to but pharmacologically distinct from mAChRs. In the current work we isolated a new type of GAR using C. elegans genome sequence information. This receptor, named GAR-2, consists of 614 amino acid residues and has seven putative transmembrane domains. Database sear
Serotonin (5-HT) plays a critical role in modulating synaptic plasticity in the marine mollusc Aplysia and in the mammalian nervous system. In Aplysia sensory neurons, 5-HT can activate several signal cascades, including PKA and PKC, presumably via distinct types of G protein-coupled receptors. However, the molecular identities of these receptors have not yet been identified. We here report the cloning and functional characterization of a 5-HT receptor that is positively coupled to adenylyl cycl
Design techniques for realizing eight 32-tap transversal filters on a single-CMOS IC are discussed. The IC is capable of processing signals at a rate of 500 million multiplications and accumulations per second, while achieving a high dynamic range. The IC contains 32 sample-and-holds, a 32*32 analog multiplexer, eight 32-input summing amplifiers, and all of the needed control circuitry. The chip was fabricated using a standard CMOS, p-well process with double polysilicon. All of the necessary an
Mutations in RAS signaling pathway components cause diverse neurodevelopmental disorders, collectively called RASopathies. Previous studies have suggested that dysregulation in RAS-extracellular signal-regulated kinase (ERK) activation is restricted to distinct cell types in different RASopathies. Some cases of Noonan syndrome (NS) are associated with gain-of-function mutations in the phosphatase SHP2 (encoded by <i>PTPN11</i>); however, SHP2 is abundant in multiple cell types, so it is unclear
We have isolated a cDNA clone from the nematode Caenorhabditis elegans that encodes a protein of greatest sequence similarity to muscarinic acetylcholine receptors. This gene codes for a polypeptide of 682 amino acids containing seven putative transmembrane domains. The amino acid identities, excluding a highly variable middle portion of the third intracellular loop, to the human m1-m5 receptors are 28-34%. When this cloned receptor was coexpressed with a G protein-gated inwardly rectifying K+ c
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