Microtubule maintenance, mechanosensation, and cytoskeletal dynamics
Microtubule tracks transport diverse cargos, such as vesicles, organelles, and chromosomes. If the tracks are broken, due to mechanical stress or exposure to toxins, traffic stops. The downstream consequences may lead to neurodegeneration, cell death, and cancer. One of our long-term goals is to understand how cells maintain microtubule integrity under mechanical and chemical stress.
Our work centers on α-tubulin acetyltransferase (αTAT), an enzyme that acetylates α-tubulin at lysine 40 within the microtubule lumen. This modification confers mechanical resilience, and protects microtubules from fatigue and breakage. Using Drosophila melanogaster, we generated animals that completely lack αTAT to study how loss of microtubule acetylation affects their development and the function of their nervous system. In these mutants, microtubules in mechanosensory neurons fracture during ordinary locomotion, with striking sensory consequences: these flies cannot sense touch, detect sound, or perceive gravity. Each of these sensory functions require αTAT-mediated protection of the microtubules in on mechanosensory neurons.
αTAT's protective role extends beyond mechanical forces. Cells lacking the enzyme are also more susceptible to chemical toxins that have been implicated in carcinogenesis and diabetes, suggesting αTAT protects microtubules from a broader range of insults than physical stress alone.
αTAT is conserved from flies to humans. Defining how it maintains microtubule integrity in Drosophila should illuminate its role in human pathology, particularly sensory neuropathies and conditions linked to chronic toxic exposure.
BIOL 240 Introduction to Cell Biology · BIOL 544L Course-based Research Experience in Diseases of the Cytoskeleton
B.S. in molecular biology from Purdue University. Ph.D. in cell biology from the University of Illinois at Urbana, studying regulation of organelle transport by microtubule motor proteins and unconventional myosins with Dr. Vladimir Gelfand. Postdoc with Dr. Ron Vale at UCSF, where he developed methods to use cultured Drosophila cells to study the actin and microtubule cytoskeletons and studied proteins that interact with microtubule plus ends to control dynamic instability and regulate signaling pathways in embryonic morphogenesis.
UNC students interested in doing research should review our active projects and read about the research experience and expectations.
Email is the best way to reach Prof. Rogers: srogers@bio.unc.edu