Research Interests
My lab uses a small roundworm, Caenorhabditis elegans, as a model system to study the assembly and structure of muscle and the control of muscle contraction by the nervous system. Several projects are available for student research. In one project, we are working to understand the role of myosin in constructing functioning muscle. Students are making mutant myosin genes that encode only portions of the myosin protein. They then micro-inject these genes into young adult worms and look at the muscle structure and function of the offspring. This work has been generously funded by the NSF-RUI program.
A second line of research is aimed at determining the role of a putative potassium channel in male mating behavior. Student in my lab previously isolating some interesting alleles of the gene sup-9, thought to encode one such potassium channel. These mutant alleles seem only to affect male worms, making them unable to mate, despite being able to move normally. Current students are investigating whether this defect is do to abberant channel activity in muscle cell membranes or in the nervous system. This work has been funded by several grants from the NIH-AREA program.
Recently, we have begun collaborating with the laboratories of Bart De Stasio (biology) and Jerry Lokensgard (chemistry) to determine the effects of a kairomone released by a predator on Daphnia morphogenesis. My lab is interested in determining the gene expression patterns of Daphnia grown in the presence kairomone. The long term goal is to link the kairomone signal to altered gene expression that then controls the formation of anti-predator morphologies (spines, neck teeth). This research is funded by an interdisciplinary grant to the biology and chemistry departments at Lawrence from AAAS/Merck.
Beth De Stasio in the lab, 2004