Merdes A, Gounari F, Georgatos S D
Cell Biology Programme, European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
J Cell Biol. 1993 Dec;123(6 Pt 1):1507-16. doi: 10.1083/jcb.123.6.1507.
In previous studies we have characterized a lens-specific intermediate filament (IF) protein, termed filensin. Filensin does not self-assemble into regular IFs but is known to associate with another 47-kD lens-specific protein which has been suggested to represent its assembly partner. To address this possibility, we cloned and sequenced the cDNA coding for the bovine 47-kD protein which we have termed phakinin (from the greek phi alpha kappa omicron sigma = phakos = lens). The predicted sequence comprises 406 amino acids and shows significant similarity (31.3% identity over 358 residues) to type I cytokeratins. Phakinin possesses a 95-residue, non-helical domain (head) and a 311 amino acid long alpha-helical domain punctuated with heptad repeats (rod). Similar to cytokeratin 19, phakinin lacks a COOH-terminal tail domain and it therefore represents the second known example of a naturally tailless IF protein. Confocal microscopy on frozen lens sections reveals that phakinin colocalizes with filensin and is distributed along the periphery of the lens fiber cells. Quantitative immunoblotting with whole lens fiber cell preparations and fractions of washed lens membranes suggest that the natural stoichiometry of phakinin to filensin is approximately 3:1. Under in vitro conditions, phakinin self-assembles into metastable filamentous structures which tend to aggregate into thick bundles. However, mixing of phakinin and filensin at an optimal ratio of 3:1 yields stable 10-nm filaments which have a smooth surface and are ultrastructurally indistinguishable from "mainstream" IFs. Immunolabeling with specific antibodies shows that these filaments represent phakinin/filensin heteropolymers. Despite its homology to the cytokeratins, phakinin does not coassemble with acidic (type I), or basic (type II) cytokeratins. From these data we conclude that filensin and phakinin are obligate heteropolymers which constitute a new membrane-associated, lens-specific filament system related to, but distinct from the known classes of IFs.
在先前的研究中,我们已对一种晶状体特异性中间丝(IF)蛋白进行了表征,该蛋白称为丝状晶状体蛋白。丝状晶状体蛋白不会自行组装成规则的中间丝,但已知它与另一种47-kD的晶状体特异性蛋白相关联,有人认为该蛋白是其组装伴侣。为了探究这种可能性,我们克隆并测序了编码牛47-kD蛋白的cDNA,我们将其称为晶状体中间丝蛋白(源自希腊语phi alpha kappa omicron sigma = phakos = 晶状体)。预测的序列包含406个氨基酸,与I型细胞角蛋白具有显著的相似性(在358个残基上有31.3%的同一性)。晶状体中间丝蛋白具有一个95个残基的非螺旋结构域(头部)和一个311个氨基酸长的α-螺旋结构域,其间穿插着七肽重复序列(杆部)。与细胞角蛋白19相似,晶状体中间丝蛋白缺乏COOH末端尾部结构域,因此它是天然无尾中间丝蛋白的第二个已知例子。对冷冻晶状体切片进行共聚焦显微镜观察发现,晶状体中间丝蛋白与丝状晶状体蛋白共定位,并沿晶状体纤维细胞的周边分布。用整个晶状体纤维细胞制剂和洗涤过的晶状体膜部分进行定量免疫印迹分析表明,晶状体中间丝蛋白与丝状晶状体蛋白的天然化学计量比约为3:1。在体外条件下,晶状体中间丝蛋白自行组装成亚稳态的丝状结构,这些结构倾向于聚集成粗束。然而,以3:1的最佳比例混合晶状体中间丝蛋白和丝状晶状体蛋白会产生稳定的10纳米细丝,其表面光滑,在超微结构上与“主流”中间丝无法区分。用特异性抗体进行免疫标记表明,这些细丝代表晶状体中间丝蛋白/丝状晶状体蛋白异源聚合物。尽管晶状体中间丝蛋白与细胞角蛋白具有同源性,但它不会与酸性(I型)或碱性(II型)细胞角蛋白共同组装。从这些数据我们得出结论,丝状晶状体蛋白和晶状体中间丝蛋白是专性异源聚合物,它们构成了一个新的与膜相关的、晶状体特异性的细丝系统,与已知的中间丝类别相关但又不同。