van der Ven P F, Wiesner S, Salmikangas P, Auerbach D, Himmel M, Kempa S, Hayess K, Pacholsky D, Taivainen A, Schröder R, Carpén O, Fürst D O
Department of Cell Biology, University of Potsdam, D-14471 Potsdam, Germany.
J Cell Biol. 2000 Oct 16;151(2):235-48. doi: 10.1083/jcb.151.2.235.
gamma-Filamin, also called ABP-L, is a filamin isoform that is specifically expressed in striated muscles, where it is predominantly localized in myofibrillar Z-discs. A minor fraction of the protein shows subsarcolemmal localization. Although gamma-filamin has the same overall structure as the two other known isoforms, it is the only isoform that carries a unique insertion in its immunoglobulin (Ig)-like domain 20. Sequencing of the genomic region encoding this part of the molecule shows that this insert is encoded by an extra exon. Transient transfections of the insert-bearing domain in skeletal muscle cells and cardiomyocytes show that this single domain is sufficient for targeting to developing and mature Z-discs. The yeast two-hybrid method was used to identify possible binding partners for the insert-bearing Ig-like domain 20 of gamma-filamin. The two Ig-like domains of the recently described alpha-actinin-binding Z-disc protein myotilin were found to interact directly with this filamin domain, indicating that the amino-terminal end of gamma-filamin may be indirectly anchored to alpha-actinin in the Z-disc via myotilin. Since defects in the myotilin gene were recently reported to cause a form of autosomal dominant limb-girdle muscular dystrophy, our findings provide a further contribution to the molecular understanding of this disease.
γ-细丝蛋白,也称为ABP-L,是一种细丝蛋白异构体,在横纹肌中特异性表达,主要定位于肌原纤维的Z线。该蛋白的一小部分位于肌膜下。尽管γ-细丝蛋白与其他两种已知异构体具有相同的整体结构,但它是唯一一种在其免疫球蛋白(Ig)样结构域20中具有独特插入序列的异构体。对编码该分子这一部分的基因组区域进行测序表明,该插入序列由一个额外的外显子编码。在骨骼肌细胞和心肌细胞中瞬时转染带有插入序列的结构域表明,这一单个结构域足以靶向发育中的和成熟的Z线。采用酵母双杂交法来鉴定γ-细丝蛋白中带有插入序列的Ig样结构域20的可能结合伴侣。最近描述的与α-辅肌动蛋白结合的Z线蛋白肌联蛋白的两个Ig样结构域被发现可直接与该细丝蛋白结构域相互作用,这表明γ-细丝蛋白的氨基末端可能通过肌联蛋白间接锚定在Z线中的α-辅肌动蛋白上。由于最近报道肌联蛋白基因缺陷会导致一种常染色体显性肢带型肌营养不良,我们的发现为该疾病的分子理解提供了进一步的贡献。