Phosphorylation-dependent power output of transgenic flies: an integrated study

• Published in: Biophysical journal Vol. 73; no. 6; pp. 3122 - 3134
• Main Authors: Dickinson, M.H., Hyatt, C.J., Lehmann, F.O., Moore, J.R., Reedy, M.C., Simcox, A., Tohtong, R., Vigoreaux, J.O., Yamashita, H., Maughan, D.W.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-12-1997
• Subjects: ANIMAL TRANSGENIQUE; ANIMALES TRANSGENICOS; Animals; Animals, Genetically Modified; Biomechanical Phenomena; Biophysical Phenomena; Biophysics; Calcium - physiology; DROSOPHILA MELANOGASTER; Drosophila melanogaster - genetics; Drosophila melanogaster - physiology; Elasticity; Female; FLIGHT MUSCLES; Flight, Animal - physiology; GLOBULINAS; GLOBULINE; GLOBULINS; In Vitro Techniques; Isometric Contraction; Microscopy, Electron; Models, Biological; MUSCLE; Muscle Fibers, Skeletal - chemistry; Muscle Fibers, Skeletal - physiology; Muscle Fibers, Skeletal - ultrastructure; MUSCLES; MUSCULOS; Mutagenesis, Site-Directed; MYOSIN LIGHT CHAIN KINASE; Myosin Light Chains - chemistry; Myosin Light Chains - physiology; Myosin Light Chains - ultrastructure; Myosin-Light-Chain Kinase - physiology; MYOSINS; Phosphorylation; PROTEIN KINASE; PROTEINA QUINASA; PROTEINE KINASE; TRANSGENIC ANIMALS; Viscosity
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(97)78338-3

We examine how the structure and function of indirect flight muscle (IFM) and the entire flight system of Drosophila melanogaster are affected by phosphorylation of the myosin regulatory light chain (MLC2). This integrated study uses site-directed mutagenesis to examine the relationship between removal of the myosin light chain kinase (MLCK) phosphorylation site, in vivo function of the flight system (flight tests, wing kinematics, metabolism, power output), isolated IFM fiber mechanics, MLC2 isoform pattern, and sarcomeric ultrastructure. The MLC2 mutants exhibit graded impairment of flight ability that correlates with a reduction in both IFM and flight system power output and a reduction in the constitutive level of MLC2 phosphorylation. The MLC2 mutants have wild-type IFM sarcomere and cross-bridge structures, ruling out obvious changes in the ultrastructure as the cause of the reduced performance. We describe a viscoelastic model of cross-bridge dynamics based on sinusoidal length perturbation analysis (Nyquist plots) of skinned IFM fibers. The sinusoidal analysis suggests the high power output of Drosophila IFM required for flight results from a phosphorylation-dependent recruitment of power-generating cross-bridges rather than a change in kinetics of the power generating step. The reduction in cross-bridge number appears to affect the way mutant flies generate flight forces of sufficient magnitude to keep them airborne. In two MLC2 mutant strains that exhibit a reduced IFM power output, flies appear to compensate by lowering wingbeat frequency and by elevating wingstroke amplitude (and presumably muscle strain). This behavioral alteration is not seen in another mutant strain in which the power output and estimated number of recruited cross-bridges is similar to that of wild type.