Drosophila Mutants with Progressive Atrophy in Dorsal Longitudinal Muscles

Abstract

We have characterized six chemically induced mutations of the Drosophila dim-defective (dlmd) gene. The mutants are flightless, but they have an otherwise normal appearance. By electron microscopic examination, a focal atrophy was found in their dorsal longitudinal muscle (DLM) fibers, but no abnormalities in nerve conduction or synaptic transmission were detected by electrophysiological tests. The nerve-evoked muscle spike also seemed to be normal, except that the resting potential of DLM in mutant flies was lower and their membrane excitability was higher than those in the wild type flies. The possible causes of the DLM degeneration in this strain are discussed.

Key Words:

• Drosophila metanogaster
• flightless mutants
• Dorsal Longitudinal Muscle (DLM)
• muscular atrophy
• neuromuscular function