Hemken P M, Bellin R M, Sernett S W, Becker B, Huiatt T W, Robson R M
Muscle Biology Group, Departments of Biochemistry and Biophysics and of Animal Science, Iowa State University, Ames, Iowa 50011-3260, USA.
J Biol Chem. 1997 Dec 19;272(51):32489-99. doi: 10.1074/jbc.272.51.32489.
Paranemin was initially found to copurify with the intermediate filament (IF) proteins vimentin and desmin from embryonic chick skeletal muscle and was described as an IF-associated protein (IFAP). We have purified paranemin from embryonic chick skeletal muscle, prepared antibodies, and demonstrated that they label at the Z-lines of both adult avian and porcine cardiac and skeletal muscle myofibrils. We determined the cDNA sequence of paranemin by immunoscreening a lambdagt22A cDNA library from embryonic chick skeletal muscle. Northern blot analysis revealed a single transcript of 5.3 kilobases, which is much smaller than predicted from the size of paranemin (280 kDa) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The derived amino acid sequence of paranemin (1,606 residues; 178,161 kDa) contains the conserved IF rod domain (308 amino acids), which has highest homology to the rod domains of nestin and tanabin. Thus, paranemin is an IF protein rather than an IFAP. Sequence analysis also revealed that the partial cDNA sequences of two proteins, namely EAP-300 and IFAPa-400, are almost identical to regions of the cDNA sequence of paranemin. The complete paranemin cDNA was expressed in a cell line (SW13) with, and without, detectable cytoplasmic IFs. Antibody labeling of these cells suggests that paranemin does not form IFs by itself, but rather is incorporated into heteropolymeric IFs with vimentin.
副肌动蛋白最初是在从胚胎鸡骨骼肌中与中间丝(IF)蛋白波形蛋白和结蛋白共纯化时被发现的,并被描述为一种IF相关蛋白(IFAP)。我们从胚胎鸡骨骼肌中纯化了副肌动蛋白,制备了抗体,并证明它们标记成年禽类和猪的心肌及骨骼肌肌原纤维的Z线。我们通过免疫筛选来自胚胎鸡骨骼肌的λgt22A cDNA文库确定了副肌动蛋白的cDNA序列。Northern印迹分析显示有一个5.3千碱基的单一转录本,这比通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳预测的副肌动蛋白大小(280 kDa)要小得多。推导的副肌动蛋白氨基酸序列(1606个残基;178,161 kDa)包含保守的IF杆状结构域(308个氨基酸),它与巢蛋白和塔纳宾的杆状结构域具有最高的同源性。因此,副肌动蛋白是一种IF蛋白而非IFAP。序列分析还显示,两种蛋白EAP - 300和IFAPa - 400的部分cDNA序列与副肌动蛋白的cDNA序列区域几乎相同。完整的副肌动蛋白cDNA在有和没有可检测到的细胞质IFs的细胞系(SW13)中表达。对这些细胞的抗体标记表明,副肌动蛋白本身并不形成IFs,而是与波形蛋白一起掺入异源多聚体IFs中。