Group:MUZIC:Plectin
IntroductionPlectin is a multidomain protein with large size (>500kDa) and versatile binding properties, which abundantly expressed in a wide variety of mammalian tissues and cell types, combined with different binding partners. It has important functions in maintaining the mechanical stability of skin, skeletal muscle and heart. The plectin gene has unusual 5'-end diversity, which is alternatively spliced into exon 2 and makes 11 kinds of isoforms. Expression level of isofroms is varied in tissues,and some of them are specifically expressed in brain (isoform 1c),skeletal muscle (isoform 1d) and skin(isoform 1a). [1].
Sequence annotationThe isoform-1 of the human plectin contains 4,684 amino acids (uniprot:Q15149). Plectin can be divided in three main sections; a central coiled-coil rod domain(exon 31), N and C-terminal globular region and exhibits a dumbbell like structure [2]. C-terminal region (exon 32) is composed of 6 homologous repeating domains, and this region has a role in binding to intermediate filaments such as vimentin and cytokeratin [3]. N-terminal globular region contains actin binding domain comprising two calponin homology (exon 2-8) and plakin domain (exon 9-30).  Schematic domain map of plectin (Winter, 2013) Structures1. Actin Binding Domain (ABD) Plectin has a canonical actin binding domain in N-terminus, which is consisted of two calponin homology domain(CH1 and CH2)[4]. N-terminal domain of plectin containing ABD interacts with F-actin and regulates actin dynamics in vivo, additionally binding of plectin ABD to vimentin was also reported [5].
2. Plakin domain The plakin domain is formed by an array of spectrin repeats (SR) and a Src-homology 3 (SH3), and harbors binding sites for junctional proteins. This region is adjacent to the actin-binding domain and is required for efficient binding to the integrin alpha6beta4 in hemidesmosomes.[6] 3. Integrin β4-Plectin complex The interaction between the integrin α6β4 and plectin is essential for the assembly and stability of hemidesmosomes, which are junctional adhesion complexes that anchor epithelial cells to the basement membrane.[7] Function and InteractionsCrystal structure of plectin ABD(magenta) and integrin beta 4 (green) complex (PDB:3f7p) Proteins coordinate various cytoskeletal networks are termed as cytolinkers, which are able to interlink different types of cytoskeletons. Plectin is one of the well-characterized cytolinker and expressed in diverse cell types and tissues, a number of different binding partners of plectin have been identified. Intermediate filament(IF) binding sites of plectin is located between plakin repeats 5 and 6 in C-terminal globular domain. Several IF proteins were identified to interact with plectin such as vimentin, desmin, GFAP(glial fibrillary acidic protein) and cytokeratins [8] . The actin binding domain(ABD)in N-terminal globular domain has a role to interact with integrin subunit beta 4 to establish mechanical stability in hemedesmosomes along with its function for binding to actin filament(F-actin). Calmodulin(CaM) is also known to bind the ABD of plectin to modulate the hemidesmosome disassembly [9]. PathologyIt has been reported that patients with EBS-MD (Epidermolysis bullosa simplex with muscular dystrophy),a genetic disorder characterized severe skin blistering disease combined with muscular dystrophy, have a muation on plectin gene(PLEC1). This mutation leads to premature termination of translation.[10] In addition, site-specific missense mutation(R2110W) on plectin rod domain causes an autosomal dominant form of disease termed EBS-Ogna without muscular dystrophy.[11] Plectin deficient(-/-) mice also exhibit similar skin and muscle phenotypes of human patients suffering from EBS-MD and died 2-3 days after birth. [12]
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Jae-Geun Song, Nikos Pinotsis, Michal Harel, Jaime Prilusky, Alexander Berchansky
