Yamaguchi M, Izumimoto M, Robson R M, Stromer M H
J Mol Biol. 1985 Aug 20;184(4):621-43. doi: 10.1016/0022-2836(85)90308-0.
A model of the structure of vertebrate Z-lines and Z-line analogs is introduced and supported by evidence from electron microscope studies of wide Z-lines (rat and feline soleus, and feline and canine cardiac muscles), narrow Z-lines (guppy, newt and frog skeletal muscles), and Z-rods (from a patient with nemaline myopathy and from cardiac muscles of aged dog). The model is based on a pair of Z-filaments (termed a Z-unit), which are linked near their centers at a 90 degrees angle and form bridges between neighboring antipolar thin (actin) filaments. A square lattice of four Z-filament pairs (the basic structure of the Z-line, termed a Z-line unit) defines the geometrical position of the I-square unit. In this native state of the Z-line, small square and large square net forms appear in cross-section. Other cross-sectional patterns of Z-lines, including basket-weave and diagonal-square net patterns, can be explained by detachment of the Z-filament from the Z-filament binding region within each Z-filament pair due to chemical or physical stress. Dissection of Z-lines and Z-line analogs with calcium-activated neutral protease provides evidence that the width of all wide Z-line structures is determined by the amount of overlap of antipolar thin filaments from adjacent sarcomeres. Longitudinal patterns of narrow and wide Z-lines are shown and described in relation to the model. To test the proposed model, the dynamics of the Z-line unit structure were computer-simulated. An attempt was made to correlate longitudinal (z direction) and cross-sectional (x and y directions) patterns and to determine the amount of movement of thin or Z-filaments that is required to explain the diversity observed in cross-sectional patterns of Z-lines. The computer simulations demonstrated that the structural transitions among the small square, and therefore large square net, as well as basket-weave and diagonal-square net forms seen in cross-sections could be caused by movements of thin filaments less than 10 nm in any direction (x, y or z).(ABSTRACT TRUNCATED AT 400 WORDS)
本文介绍了脊椎动物Z线和Z线类似物的结构模型,并得到了来自宽Z线(大鼠和猫的比目鱼肌,以及猫和犬的心肌)、窄Z线(孔雀鱼、蝾螈和青蛙的骨骼肌)和Z小体(来自一名杆状肌病患者以及老年犬的心肌)的电子显微镜研究证据的支持。该模型基于一对Z细丝(称为一个Z单元),它们在中心附近以90度角相连,并在相邻的反极细(肌动蛋白)丝之间形成桥。由四个Z细丝对组成的方形晶格(Z线的基本结构,称为一个Z线单元)定义了I方形单元的几何位置。在Z线的这种天然状态下,横截面中会出现小方形和大方形网络形式。Z线的其他横截面模式,包括篮状编织和对角方形网络模式,可以通过化学或物理应力导致Z细丝从每个Z细丝对中的Z细丝结合区域脱离来解释。用钙激活中性蛋白酶对Z线和Z线类似物进行解剖,提供了证据表明所有宽Z线结构的宽度由相邻肌节的反极细肌丝的重叠量决定。展示并描述了窄Z线和宽Z线与该模型相关的纵向模式。为了测试所提出的模型,对Z线单元结构的动力学进行了计算机模拟。试图将纵向(z方向)和横截面(x和y方向)模式相关联,并确定解释Z线横截面模式中观察到的多样性所需的细肌丝或Z细丝的移动量。计算机模拟表明,横截面中看到的从小方形到大方形网络,以及篮状编织和对角方形网络形式之间的结构转变可能是由细肌丝在任何方向(x、y或z)上小于10纳米的移动引起的。(摘要截断于400字)