Chang Sung

 Chang Sung

Chang Sung

  • Courses1
  • Reviews1

Biography

Texas A&M University Kingsville - Biology


Resume

  • 1999

    English

    Korean

    PhD

    Molecular Biology

    University of Illinois at Chicago

  • 1997

    MS

    Biology

    Illinois Institute of Technology

    Biotechnology

    Molecular Biology

  • Purification of nucleic acid from mammalian cells and tissues

    Small RNA isolation

    Cell Biology

    Translational Research

    FACS Analysis

    Mammalian cell culture

    Quantitative real-time PCR-based RNA array

    Polyoma

    Retro and Lenti virus cloning and production

    Virus

    Immunofluorescence analysis of tissues

    Protein Purification

    Cancer Research

    Cancer

    Animal Models

    Detection of apoptotic cells with luciferase gene reporter and TUNEL assays

    in vitro/vivo ubiquitination assays

    Transformations

    Transfection and molecular cloning

    Analysis of Bisulfite converted DNAs with biotin pulldowns and pyrosequencing

    Cell Culture

    Chromatin immunoprecipitation

    Transcriptional and Post-translational Regulation of the Quiescence Factor and Putative Tumor Suppressor p150Sal2.

    Sung and Dahl contributed equally to this work

    Benjamin TL

    Rodig S

    Yim H

    Dahl J

    In both growing fibroblasts and established ovarian surface epithelial cells

    p150Sal2 undergoes polyubiquitination and proteosomal degradation. A CUL4/DDB1 E3 ligase containing RBBP7 as the p150Sal2 receptor has been identified as mediating the destruction of p150Sal2 as cells transition from a quiescent to an actively growing state.

    Transcriptional and Post-translational Regulation of the Quiescence Factor and Putative Tumor Suppressor p150Sal2.

    Polyoma Virus-Induced Osteosarcomas in Inbred Strains of Mice: Host Determinants of Metastasis.

    Velupillai and Sung contributed equally to this work

    Benjamin TL

    Bronson R

    Carroll J

    Dahl J

    Tian Y

    Velupillai P

    Comparing osteosarcoma cell lines from two different mouse starins

    we have identified a molecular pathway that underlies invasive behavior in vitro and correlates with metastasis in vivo.

    Polyoma Virus-Induced Osteosarcomas in Inbred Strains of Mice: Host Determinants of Metastasis.

    Sullivan and Sung contributed equally to this work

    Ganem D

    Benjamin TL

    Lukacher AE

    Grundhoff A

    Pack CD

    Sullivan CS

    We showed that PyV encodes a pre-miRNA during infection that is processed into two stable miRNAs

    and explored the functions of these miRNAs both in culture and experimental inoculation of mice.

    Murine Polyomavirus Encodes a MicroRNA That Cleaves Early RNA Transcripts But is Not Essential For Experimental Infection.

    Chang

    Sung

    Texas A&M University-Kingsville

    University of Illinois at Chicago

    Harvard Medical School

    Texas A&M University-Kingsville

    Research Fellow

    -Characterized ubiquitin-mediated regulation of a tumor suppressor p150Sal2\n-Identified and characterized a set of microRNAs encoded by the oncogenic polyoma virus\n-Analyzed the mechanisms of bone tumor metastasis during the mouse polyoma virus infection\n-Determined that the levels of TAZ and its kinase Nek1 are critical for polycystic kidney disease (PKD)

    Harvard Medical School

    Graduate Researcher

    -Developed new pneumococcal mutagenesis methods

    which have since been applied to many transformable streptococcal strains\n-Identified new genes in response to the competence pheromone by DNA microarrays\n-Performed functional analysis of ComW

    one of the new competence factors

    University of Illinois at Chicago

    Instructor

    -Guided and supervised junior researchers and students to develop various research projects\n-Screen de-ubiquitinating enzymes (DUBs) that may preserve a tumor suppressor p150Sal2\nin normal human ovarian surface epithelial cells\n-Examine epigenetic silencing (promoter methylation) of a tumor suppressor p150Sal2\nin human ovarian carcinomas\n-Screen murine non-coding RNAs in response to oncogenic polyoma virus infection\nto identify novel biomolecular markers involved in oncogenesis and tumor progression\n-Investigate how polymorphisms in toll-like receptor 4 (Tlr4) lead to different cytokine responses

    Harvard Medical School

    Associate Professor

    Texas A&M University-Kingsville