Suggs Jennifer A, Cammarato Anthony, Kronert William A, Nikkhoy Massoud, Dambacher Corey M, Megighian Aram, Bernstein Sanford I
Department of Biology, Molecular Biology Institute and SDSU Heart Institute, San Diego State University, San Diego, CA 92182-4614, USA.
J Mol Biol. 2007 Apr 13;367(5):1312-29. doi: 10.1016/j.jmb.2007.01.045. Epub 2007 Jan 23.
Muscle myosin heavy chain (MHC) rod domains intertwine to form alpha-helical coiled-coil dimers; these subsequently multimerize into thick filaments via electrostatic interactions. The subfragment 2/light meromyosin "hinge" region of the MHC rod, located in the C-terminal third of heavy meromyosin, may form a less stable coiled-coil than flanking regions. Partial "melting" of this region has been proposed to result in a helix to random-coil transition. A portion of the Drosophila melanogaster MHC hinge is encoded by mutually exclusive alternative exons 15a and 15b, the use of which correlates with fast (hinge A) or slow (hinge B) muscle physiological properties. To test the functional significance of alternative hinge regions, we constructed transgenic fly lines in which fast muscle isovariant hinge A was switched for slow muscle hinge B in the MHC isoforms of indirect flight and jump muscles. Substitution of the slow muscle hinge B impaired flight ability, increased sarcomere lengths by approximately 13% and resulted in minor disruption to indirect flight muscle sarcomeric structure compared with a transgenic control. With age, residual flight ability decreased rapidly and myofibrils developed peripheral defects. Computational analysis indicates that hinge B has a greater coiled-coil propensity and thus reduced flexibility compared to hinge A. Intriguingly, the MHC rod with hinge B was approximately 5 nm longer than myosin with hinge A, consistent with the more rigid coiled-coil conformation predicted for hinge B. Our study demonstrates that hinge B cannot functionally substitute for hinge A in fast muscle types, likely as a result of differences in the molecular structure of the rod, subtle changes in myofibril structure and decreased ability to maintain sarcomere structure in indirect flight muscle myofibrils. Thus, alternative hinges are important in dictating the distinct functional properties of myosin isoforms and the muscles in which they are expressed.
肌肉肌球蛋白重链(MHC)的杆状结构域相互缠绕形成α-螺旋卷曲螺旋二聚体;这些二聚体随后通过静电相互作用多聚化形成粗肌丝。MHC杆状结构的亚片段2/轻酶解肌球蛋白“铰链”区域位于重酶解肌球蛋白的C端三分之一处,与侧翼区域相比,可能形成稳定性较低的卷曲螺旋。有人提出该区域的部分“解链”会导致螺旋向无规卷曲的转变。果蝇MHC铰链的一部分由互斥的可变外显子15a和15b编码,其使用与快肌(铰链A)或慢肌(铰链B)的生理特性相关。为了测试可变铰链区域的功能意义,我们构建了转基因果蝇品系,其中间接飞行肌和跳跃肌的MHC异构体中,快肌异构体的铰链A被慢肌铰链B替换。与转基因对照相比,慢肌铰链B的替换损害了飞行能力,使肌节长度增加了约13%,并导致间接飞行肌肌节结构出现轻微破坏。随着年龄的增长,残余飞行能力迅速下降,肌原纤维出现外周缺陷。计算分析表明,与铰链A相比,铰链B具有更大的卷曲螺旋倾向,因此柔韧性降低。有趣的是,带有铰链B的MHC杆比带有铰链A的肌球蛋白长约5纳米,这与预测的铰链B更刚性的卷曲螺旋构象一致。我们的研究表明,在快肌类型中,铰链B不能在功能上替代铰链A,这可能是由于杆状结构分子结构的差异、肌原纤维结构的细微变化以及间接飞行肌肌原纤维中维持肌节结构能力的下降。因此,可变铰链在决定肌球蛋白异构体及其所表达肌肉的不同功能特性方面很重要。