Duane A. Compton, PhD
Professor of Biochemistry & Cell Biology
Dean of the Medical School
Biochemistry & Cell Biology
U. Oklahoma, BS 1984
U. Texas, PHD 1988
Academy of Master Faculty Educators
Molecular and Cellular Biology Graduate Programs
Geisel School of Medicine at Dartmouth
Hanover NH 03755
Work in this lab is aimed at understanding how chromosomes segregate efficiently during mitosis and meiosis in vertebrate cells. Using both in vitro and in vivo approaches, the assembly and function of the microtubule-based spindle is being dissected at the molecular level. This work has led to the characterization of both structural and motor proteins that are necessary for the organization of the microtubules into spindles during mitosis and meiosis. Current work is aimed at how this process is regulated during the cell cycle and at how these proteins coordinate chromosome movement during cell division.
Duane has contributed lectures and small group discussions to Biochem 110, the Biochemical and Genetic Basis of Medicine, for first year medical students. He served as course director for Biochem 110 for many years. Duane also contributed lectures to Biochem 103, the third term of the MCB core course for first year graduate students. He served as course director for that course for many years. Duane has mentored 13 graduate students to the completion of their PhDs.
Duane would be happy to mentor faculty about teaching in large or small group environments, directing a course, and mentoring graduate students.
Quantitative methods to measure aneuploidy and chromosomal instability.
Cyclin A/Cdk1 modulates Plk1 activity in prometaphase to regulate kinetochore-microtubule attachment stability.
Mitotic DNA Damage Response: At the Crossroads of Structural and Numerical Cancer Chromosome Instabilities.
Adaptive Resistance to an Inhibitor of Chromosomal Instability in Human Cancer Cells.
Dinaciclib Induces Anaphase Catastrophe in Lung Cancer Cells via Inhibition of Cyclin-Dependent Kinases 1 and 2.
Chromosomal Instability Affects the Tumorigenicity of Glioblastoma Tumor-Initiating Cells.
Intact Cohesion, Anaphase, and Chromosome Segregation in Human Cells Harboring Tumor-Derived Mutations in STAG2.
Specific CP110 Phosphorylation Sites Mediate Anaphase Catastrophe after CDK2 Inhibition: Evidence for Cooperation with USP33 Knockdown.
Shugoshin-1 balances Aurora B kinase activity via PP2A to promote chromosome bi-orientation.
CDK2 Inhibition Causes Anaphase Catastrophe in Lung Cancer through the Centrosomal Protein CP110.