Sonnenberg Arnoud, Liem Ronald K H
Division of Cell Biology, The Netherlands Cancer Inst., Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Exp Cell Res. 2007 Jun 10;313(10):2189-203. doi: 10.1016/j.yexcr.2007.03.039. Epub 2007 Apr 19.
Plakins are large multi-domain molecules that have various functions to link cytoskeletal elements together and to connect them to junctional complexes. Plakins were first identified in epithelial cells where they were found to connect the intermediate filaments to desmosomes and hemidesmosomes [Ruhrberg, C., and Watt, F.M. (1997). The plakin family: versatile organizers of cytoskeletal architecture. Curr Opin Genet Dev 7, 392-397.]. They were subsequently found to be important for the integrity of muscle cells. Most recently, they have been found in the nervous system, where their functions appear to be more complex, including cross-linking of microtubules (MTs) and actin filaments [Leung, C.L., Zheng, M., Prater, S.M., and Liem, R.K. (2001). The BPAG1 locus: Alternative splicing produces multiple isoforms with distinct cytoskeletal linker domains, including predominant isoforms in neurons and muscles. J Cell Biol 154, 691-697., Leung, C.L., Sun, D., Zheng, M., Knowles, D.R., and Liem, R.K. (1999). Microtubule actin cross-linking factor (MACF): a hybrid of dystonin and dystrophin that can interact with the actin and microtubule cytoskeletons. J Cell Biol 147, 1275-1286.]. These plakins have also indicated their relationship to the spectrin superfamily of proteins and the plakins appear to be evolutionarily related to the spectrins, but have diverged to perform different specialized functions. In invertebrates, a single plakin is present in both Drosophila melanogaster and Caenorhabditis elegans, which resemble the more complex plakins found in mammals [Roper, K., Gregory, S.L., and Brown, N.H. (2002). The 'spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families. J Cell Sci 115, 4215-4225.]. In contrast, there are seven plakins found in mammals and most of them have alternatively spliced forms leading to a very complex group of proteins with potential tissue specific functions [Jefferson, J.J., Leung, C.L., and Liem, R.K. (2004). Plakins: goliaths that link cell junctions and the cytoskeleton. Nat Rev Mol Cell Biol 5, 542-553.]. In this review, we will first describe the plakins, desmoplakin, plectin, envoplakin and periplakin and then describe two other mammalian plakins, Bullous pemphigoid antigen 1 (BPAG1) and microtubule actin cross-linking factor 1 (MACF1), that are expressed in multiple isoforms in different tissues. We will also describe the relationship of these two proteins to the invertebrate plakins, shortstop (shot) in Drosophila and VAB-10 in C. elegans. Finally, we will describe an unusual mammalian plakin, called epiplakin.
斑联蛋白是一类大型的多结构域分子,具有多种功能,可将细胞骨架成分连接在一起,并将它们连接到连接复合体上。斑联蛋白最初是在上皮细胞中被鉴定出来的,人们发现它们能将中间丝连接到桥粒和半桥粒上[鲁尔贝格,C.,和瓦特,F.M.(1997年)。斑联蛋白家族:细胞骨架结构的多功能组织者。《当代遗传学与发育学观点》7,392 - 397页。]。随后发现它们对肌肉细胞的完整性很重要。最近,它们在神经系统中也被发现,其功能似乎更为复杂,包括微管(MTs)和肌动蛋白丝的交联[梁,C.L.,郑,M.,普拉特,S.M.,和利姆,R.K.(2001年)。BPAG1位点:可变剪接产生多种具有不同细胞骨架连接结构域的异构体,包括在神经元和肌肉中的主要异构体。《细胞生物学杂志》154,691 - 697页。,梁,C.L.,孙,D.,郑,M.,诺尔斯,D.R.,和利姆,R.K.(1999年)。微管肌动蛋白交联因子(MACF):肌营养不良素相关蛋白和肌营养不良蛋白的杂交体,可与肌动蛋白和微管细胞骨架相互作用。《细胞生物学杂志》147,1275 - 1286页。]。这些斑联蛋白还表明了它们与血影蛋白超家族蛋白质的关系,并且斑联蛋白似乎在进化上与血影蛋白相关,但已经分化以执行不同的特殊功能。在无脊椎动物中,果蝇和秀丽隐杆线虫中都存在单一的斑联蛋白,它们类似于在哺乳动物中发现的更为复杂的斑联蛋白[罗珀,K.,格雷戈里,S.L.,和布朗,N.H.(2002年)。“光谱斑联蛋白”:兼具血影蛋白和斑联蛋白家族特征的细胞骨架巨分子。《细胞科学杂志》115,4215 - 4225页。]。相比之下,在哺乳动物中发现了七种斑联蛋白,其中大多数具有可变剪接形式,导致一组非常复杂的蛋白质,可能具有组织特异性功能[杰斐逊,J.J.,梁,C.L.,和利姆,R.K.(2004年)。斑联蛋白:连接细胞连接和细胞骨架的巨人。《自然评论:分子细胞生物学》5,542 - 553页。]。在这篇综述中,我们将首先描述斑联蛋白、桥粒斑联蛋白、网蛋白、内斑联蛋白和周斑联蛋白,然后描述另外两种在不同组织中以多种异构体形式表达的哺乳动物斑联蛋白,大疱性类天疱疮抗原1(BPAG1)和微管肌动蛋白交联因子1(MACF1)。我们还将描述这两种蛋白质与无脊椎动物斑联蛋白,果蝇中的短停蛋白(shot)和秀丽隐杆线虫中的VAB - 10的关系。最后,我们将描述一种不寻常的哺乳动物斑联蛋白,称为表皮斑联蛋白。