The Curriculum in Genetics and Molecular Biology (the Genetics Curriculum) is a well-established and highly-ranked interdepartmental PhD program at the University of North Carolina at Chapel Hill (UNC-CH). Throughout the 50-year life of the program we have provided diverse and cutting-edge research opportunities to trainees. In addition to our ongoing expertise in key areas in genetics (e.g., genetics of model microbes, plants, and animals) and molecular biology (e.g., signal transduction, gene expression, and virology), we have added strengths in epigenetics, clinical and translational genetics, systems genetics, quantitative genetics, computational genetics, and genomics. Extensive interaction between researchers in diverse areas is promoted by the interdepartmental and inter-school nature of the Genetics Curriculum and many faculty centers, and is facilitated by the physical proximity of the different units, all of which are on the same campus. We strive to maintain a modern and innovative training program. The curriculum includes features common in similar programs, like coursework, written and oral qualifying exams, seminars, and retreats. Several years ago we introduced an innovative feature wherein selection of student and postdoctoral speakers for the annual Genetics Scientific Retreat are made by a mock study section at which training grant-appointed students score and discuss submitted abstracts. We've also innovated in coursework by transitioning to focused, modular courses that meet for a third of a semester and can be taken a la carte. This gives students greater flexibility choosing the most appropriate topics of study and allows faculty to teach withi their areas of greatest expertise. We now partner with the Department of Biology to expand teaching assistantship opportunities to include undergraduate courses at the introductory and advanced levels. The Office of Graduate Education has developed unique programs that enhance the training experience and promote career development. We compete nationally for the top students and have successfully recruited a diverse group, with about 25% belonging to one of the NIH-defined diversity groups. Our students are successful in obtain competitive external funding, and every student publishes at least one first-authored research paper in a peer-reviewed journal (the mean is almost 4 publications). The vast majority of our students remain in scientific careers after they graduate. Most initially do postdoctoral research in academia, government labs, or private research foundations. Some remain in academic/government research, but others go into private corporations, science teaching, or science policy.

Public Health Relevance

Genetics and genomics are among the most important fields in basic biomedical research, contributing to essentially all medical applications. The Curriculum in Genetics and Molecular Biology is a highly-ranked doctoral program that trains students broadly in these fields; this proposal seeks to continue NIH support for training these students for a careers and academic, government, and private research, clinical settings, teaching, and other scientific fields.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM007092-42
Application #
9054121
Study Section
Training and Workforce Development Subcommittee - D (TWD)
Program Officer
Haynes, Susan R
Project Start
1975-07-01
Project End
2020-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
42
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Keith, Benjamin P; Barrow, Jasmine B; Toyonaga, Takahiko et al. (2018) Colonic epithelial miR-31 associates with the development of Crohn's phenotypes. JCI Insight 3:
Liu, Yong; Leslie, Patrick L; Jin, Aiwen et al. (2018) p32 regulates ER stress and lipid homeostasis by down-regulating GCS1 expression. FASEB J 32:3892-3902
Brady, Morgan M; McMahan, Susan; Sekelsky, Jeff (2018) Loss of Drosophila Mei-41/ATR Alters Meiotic Crossover Patterning. Genetics 208:579-588
Armstrong, Robin L; Penke, Taylor J R; Strahl, Brian D et al. (2018) Chromatin conformation and transcriptional activity are permissive regulators of DNA replication initiation in Drosophila. Genome Res 28:1688-1700
Meganck, Rita M; Borchardt, Erin K; Castellanos Rivera, Ruth M et al. (2018) Tissue-Dependent Expression and Translation of Circular RNAs with Recombinant AAV Vectors In Vivo. Mol Ther Nucleic Acids 13:89-98
Chiarella, Anna M; Wang, Tiffany A; Butler, Kyle V et al. (2018) Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers. J Vis Exp :
Leslie, Patrick L; Franklin, Derek A; Liu, Yong et al. (2018) p53 Regulates the Expression of LRP1 and Apoptosis through a Stress Intensity-Dependent MicroRNA Feedback Loop. Cell Rep 24:1484-1495
Pryor, John M; Conlin, Michael P; Carvajal-Garcia, Juan et al. (2018) Ribonucleotide incorporation enables repair of chromosome breaks by nonhomologous end joining. Science 361:1126-1129
Hathaway, Nicholas J; Parobek, Christian M; Juliano, Jonathan J et al. (2018) SeekDeep: single-base resolution de novo clustering for amplicon deep sequencing. Nucleic Acids Res 46:e21
Butler, Kyle V; Chiarella, Anna M; Jin, Jian et al. (2018) Targeted Gene Repression Using Novel Bifunctional Molecules to Harness Endogenous Histone Deacetylation Activity. ACS Synth Biol 7:38-45

Showing the most recent 10 out of 266 publications