The nesprins are giant actin-binding proteins, orthologous to Drosophila melanogaster muscle protein MSP-300

被引:165
作者
Zhang, QP
Ragnauth, C
Greener, MJ
Shanahan, CM
Roberts, RG
机构
[1] Guys Hosp, GKT Med Sch, Div Med & Mol Genet, London SE1 9RT, England
[2] Univ Cambridge, Addenbrookes Hosp, Div Cardiovasc Med, Dept Med, Cambridge CB2 2QQ, England
关键词
nesprin; SYNE-1; nuclear envelope; actin-binding proteins; sarcomere; spectrin repeat; dystrophin; MSP-300; muscular dystrophy; lamin; emerin;
D O I
10.1006/geno.2002.6859
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nesprin-1 and nesprin-2 (also known as Syne-1 and Syne-2,) are large (similar to 3300-residue) vertebrate proteins associated with emerin and lamin A at the nuclear envelope of muscle cells and other cell types. We show that the previously described nesprins are short isoforms of giant proteins comprising an actin-binding amino-terminus connected to a carboxy-terminal klarsicht-related transmembrane domain by a massive (similar to 6000-8000 amino acid) spectrin-like rod domain, making full-length nesprin-1, at one megadalton, the largest non-titin protein hitherto described in humans. We find that MSP-300, a 7000-residue Drosophila melanogaster protein whose disruption results in defects of muscle development, corresponds to the N-terminal two-thirds of the Drosophila nesprin ortholog.:A nesprin-like protein is also encoded by the nematode genome. Moreover, we demonstrate that the larger isoforms of nesprin-1, like MSP-300, are localized to the sarcomeric Z-line of both skeletal and cardiac muscle. The recognition that a characteristic muscle-specific mutant phenotype in the fly results from a disruption of its nesprin ortholog reinforces the candidacy of the human proteins for involvement in genetic diseases of skeletal and cardiac muscle.
引用
收藏
页码:473 / 481
页数:9
相关论文
共 33 条
[1]   THE STRUCTURAL AND FUNCTIONAL DIVERSITY OF DYSTROPHIN [J].
AHN, AH ;
KUNKEL, LM .
NATURE GENETICS, 1993, 3 (04) :283-291
[2]   Syne-1, a dystrophin- and klarsicht-related protein associated with synaptic nuclei at the neuromuscular junction [J].
Apel, ED ;
Lewis, RM ;
Grady, RM ;
Sanes, JR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :31986-31995
[3]   THE MOUSE DYSTONIA MUSCULORUM GENE IS A NEURAL ISOFORM OF BULLOUS PEMPHIGOID ANTIGEN-1 [J].
BROWN, A ;
BERNIER, G ;
MATHIEU, M ;
ROSSANT, J ;
KOTHARY, R .
NATURE GENETICS, 1995, 10 (03) :301-306
[4]  
Delaunay J, 1996, ANN GENET-PARIS, V39, P209
[5]   Structure of the α-actinin rod:: Molecular basis for cross-linking of actin filaments [J].
Djinovic-Carugo, K ;
Young, P ;
Gautel, M ;
Saraste, M .
CELL, 1999, 98 (04) :537-546
[6]  
Fairley EAL, 2002, J CELL SCI, V115, P341
[7]  
Felsenstein J., 1989, CLADISTICS, V5, P164, DOI DOI 10.1111/J.1096-0031.1989.TB00562.X
[8]   Functional genomic analysis of C-elegans chromosome I by systematic RNA interference [J].
Fraser, AG ;
Kamath, RS ;
Zipperlen, P ;
Martinez-Campos, M ;
Sohrmann, M ;
Ahringer, J .
NATURE, 2000, 408 (6810) :325-330
[9]   Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis [J].
Kaplan, JM ;
Kim, SH ;
North, KN ;
Rennke, H ;
Correia, LA ;
Tong, HQ ;
Mathis, BJ ;
Rodríguez-Pérez, JC ;
Allen, PG ;
Beggs, AH ;
Pollak, MR .
NATURE GENETICS, 2000, 24 (03) :251-256
[10]   THE COMPLETE SEQUENCE OF DYSTROPHIN PREDICTS A ROD-SHAPED CYTOSKELETAL PROTEIN [J].
KOENIG, M ;
MONACO, AP ;
KUNKEL, LM .
CELL, 1988, 53 (02) :219-228