이성영 교수
Seongyeong Lee
서울대학교 · 생화학·유전·분자생물학
연구실 소개
이성영 교수의 연구실은 반도체 소자 기술과 생물의학 분야를 융합한 다학제적 연구를 수행하고 있습니다. 고성능 3차원 다브릿지채널 MOSFET(MBCFET)의 설계 및 제조 기술을 개발하여 나노스케일 반도체 소자의 성능 한계를 초월하고 있으며, 동시에 Wnt 신호전달 경로 및 AP-1 전사인자와 같은 핵심 유전자 조절 메커니즘을 규명하여 결장암을 비롯한 암 치료의 새로운 타겟을 모색하고 있습니다. 특히, 유전자 희귀변이 분석을 위한 고성능 통계모델 PHARAOH 개발을 통해 유전체 시퀀싱 데이터의 임상적 활용 가능성을 높이고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15We have demonstrated a novel three-dimensional multibridge-channel metal-oxide-semiconductor field-effect transistor (MBCFET). This transistor was successfully fabricated using a conventional complementary metal-oxide-semiconductor process. We introduce the fabrication technologies and electrical characteristics of MBCFET in comparison with a conventional planar MOSFET. The MBCFET has more benefits than a conventional MOSFET. It shows 4.6 times larger current drivability than a planar MOSFET. Th
The Wnt pathway is a promising therapeutic and preventive target in various human cancers. The transcriptional complex of β-catenin-T-cell factor (Tcf), a key mediator of canonical Wnt signaling, has been implicated in human colon cancer development. Current treatment of colon cancer depends on traditional cytotoxic agents with limited effects. Therefore, the identification of natural compounds that can disrupt the β-catenin-TcF complex to suppress cancer cell growth with fewer adverse side effe
Abstract Motivation To address ‘missing heritability’ issue, many statistical methods for pathway-based analyses using rare variants have been proposed to analyze pathways individually. However, neglecting correlations between multiple pathways can result in misleading solutions, and pathway-based analyses of large-scale genetic datasets require massive computational burden. We propose a Pathway-based approach using HierArchical components of collapsed RAre variants Of High-throughput sequencing
Activator protein-1 (AP-1) regulates a wide range of cellular processes including proliferation, differentiation, and apoptosis. As a transcription factor, AP-1 is commonly found as a heterodimer comprised of c-Jun and c-Fos proteins. However, other heterodimers may also be formed. The function of these dimers, specifically the heterodimeric AP-1 comprised of JunD and c-Fos (AP-1(JunD/c-Fos)), has not been elucidated. Here, we identified a function of AP-1(JunD/c-Fos) in Xenopus hematopoiesis. A
The heterodimeric c-Jun/c-Fos, an activator protein-1 (AP-1) has been implicated in mesoderm induction (Dong et al., 1996; Kim et al., 1998) whereas the homodimer of c-Jun was reported to be involved in neural inhibition during the early development of Xenopus embryos. During the early vertebrate development AP-1 involvement in the neural induction is still not clearly understood. We report here that AP-1 has a role in Zic3 expression, a critical proneural gene and a primary regulator of neural
We demonstrate highly manufacturable sub-50 nm MBCFET with the I/sub on/ of 4.26 mA/ /spl mu/m at V/sub DD/ = 1.2V, which is the best performance ever reported. This excellent performance of the MBCFET is resulted from the vertically stacked channels and enhanced mobility. It has been fabricated on bulk Si substrate by using the multiple epitaxial growth of SiGe/Si/SiGe/Si layers and damascene gate process. It has structural and electrical merits in scaling and process integration.
메밀 속성장 유래 세포외효소(protease, amylase, cellulase, lipase, xylanase) 분비능이 우수한 균주를 분리하여 혈전 용해능, 항균 활성 및 내염성을 분석하였다. 선발된 균주 중 HJ0-3을 비롯한 13개 균주는 표준 균주 B. subtilis KACC 10114보다 우수한 protease 활성을 보였다. Amylase 분비능의 경우, HJ18-4을 포함한 10개 균주는 표준 균주 B. subtilis KACC 10114보다 우수한 효소 활성을 보였다. HJ11-19 등 5균주는 표준 균주 B. subtilis KACC 10114보다 cellulase 분비능이 우수함을 확인할 수 있었다. 선별된 23개 균주 중에서 HJ5-21(21.12%), HJ18-4(86.11%), HJ18-9(31.16%), HJ18-13(63.80%)가 높은 혈전 용해능을 보였다. 선별된 23개 균주 중, 5개 균주(HJ18-4, HJ18-9, HJ18-13, HJ25-6,
Comparison with existing toolsets showed that WISARD is computationally suitable for integrated analysis of related subjects, and demonstrated that WISARD outperforms existing toolsets. WISARD has also been successfully utilized to analyze the large-scale massive sequencing dataset of chronic obstructive pulmonary disease data (COPD), and we identified multiple genes associated with COPD, which demonstrates its practical value.
A role for histone H2AX, one of the variants of the nucleosome core histone H2A, has been demonstrated in DNA repair, tumor suppression, apoptosis, and cell cycle checkpoint function. However, the physiological function and post-translational modification of histone H2AX during vertebrate development have not been elucidated. Here, we provide evidence showing that Xenopus histone H2AX (XH2AX) has a role in the anterior neural plate for eye field formation during Xenopus embryogenesis. A loss-of-
Herein, we present a powerful, pathway-based approach to investigate associations between multiple pathways and multiple phenotypes. By reflecting the natural hierarchy of biological behavior, and considering correlation between pathways and phenotypes, the proposed method is capable of analyzing multiple phenotypes and multiple pathways simultaneously.
AP-1(c-Jun/c-Fos) plays a specific role in organizer gene expression in downstream of activin signal during early Xenopus embryogenesis.
In this paper, we introduced a novel pathway-level association test by combining hierarchical structured components analysis and penalized generalized estimating equations. The proposed method analyzes all pathways in a single unified model while considering their correlations. C/C++ implementation of PHARAOH-GEE is publicly available at http://statgen.snu.ac.kr/software/pharaoh-gee/ .
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