| Popis: |
The myosin converter has been proposed to be critical for setting muscle shortening velocity by influencing the amplification of small conformational changes at the ATPase site into the larger lever arm swing. To test this hypothesis, we exploited the natural variation of the converter region found in Drosophila muscle types. In Drosophila, a single myosin heavy chain gene is alternatively spliced to generate myosin isoforms. The converter region is encoded by five alternative versions of exon 11 that are expressed in different muscle types. Through genetic modification we forced the expression of the alternative versions in the Drosophila jump muscle and found that two of the three versions tested to date, 11a (native to indirect flight muscles) and 11e (embryonic muscles), caused faster maximum shortening velocities of skinned jump muscle fibers relative to the native control 11c. Increases in velocity were primarily responsible for 70.9% and 79.0% higher power outputs for 11a and 11e fibers, respectively, because maximum force generation was not significantly different from control fibers. The fibers expressing 11a and 11e also exhibited a straighter force-velocity curve, as shown by increased Hill equation parameters a (95.4% and 84.5% higher, respectively) and b (72.6% and 65.5% higher, respectively) relative to control fibers, indicating that the converter modulates load dependent cross-bridge kinetics. The higher power and shortening velocity of 11a and 11e fibers enabled increased jumping ability, 76.0% and 48.8% farther, respectively. Converter homology models, using the new Drosophila myosin S1 crystal structure (pdb 4QBD), revealed minimal tertiary structure differences suggesting residue specific interactions with the relay, N-terminus, or essential light chain are critical. Overall, our data support the hypothesis that the converter helps set muscle shortening velocity under loaded and unloaded conditions and thus contributes to muscle fiber type diversity. |
