Peckham M, Young P, Gautel M
European Molecular Biology Laboratory, Structural Biology Division, Heidelberg, Germany.
Cell Struct Funct. 1997 Feb;22(1):95-101. doi: 10.1247/csf.22.95.
The giant muscle protein titin (connectin) is assumed to play a crucial role in the control of Z-disk assembly. Analysis of the Z-disk region of titin/connectin revealed a novel 45 residue repeat that is spliced in variable copy numbers. The repeat region is coexpressed in normal human myocardium in size variants corresponding to between 5 and 7 repeats. Smaller isoforms can be detected in muscles with thinner Z-disks like M. psoas. Sequence analysis of chicken breast muscle titin/connectin reveals that in this tissue, where Z-disks are thin, only two Z-repeats are expressed. The greatly variable thickness of Z-disks is therefore correlated to a region of variable length in titin/connectin, constructed from a novel protein building block. Transfection experiments in myogenic cell lines demonstrate that overexpression of the entire integral Z-disk region of titin leads to a disruption of sarcomere assembly. The differentially expressed titin/connectin regions, however, show no dominant-negative effects on myofibril assembly and are not targeted to Z-disks. This supports the idea that the Z-repeat region of titin/connectin is responsible for the control Z-disk thickness as an element of highly variable length, due to extensive differential splicing.
巨大的肌蛋白肌联蛋白(连接蛋白)被认为在Z盘组装的控制中起关键作用。对肌联蛋白/连接蛋白的Z盘区域分析揭示了一种新的45个残基的重复序列,其以可变的拷贝数进行剪接。该重复区域在正常人心肌中以对应于5至7个重复的大小变体共表达。在像腰大肌这样Z盘较薄的肌肉中可以检测到较小的异构体。鸡胸肌肌联蛋白/连接蛋白的序列分析表明,在这个Z盘较薄的组织中,只表达两个Z重复序列。因此,Z盘厚度的极大变化与肌联蛋白/连接蛋白中由一种新型蛋白质构建块构成的可变长度区域相关。在成肌细胞系中的转染实验表明,肌联蛋白整个完整Z盘区域的过表达会导致肌节组装的破坏。然而,差异表达的肌联蛋白/连接蛋白区域对肌原纤维组装没有显性负效应,并且不会靶向Z盘。这支持了这样一种观点,即由于广泛的差异剪接,肌联蛋白/连接蛋白的Z重复区域作为一个长度高度可变的元件,负责控制Z盘的厚度。