Nspl1, a new Z-band-associated protein

被引:12
作者
Geisler, JG
Palmer, RJ
Stubbs, LJ
Mucenski, ML
机构
[1] Univ Tennessee, Grad Sch Biomed Sci, Knoxville, TN 37932 USA
[2] Univ Tennessee, Ctr Environm Biotechnol, Knoxville, TN 37932 USA
[3] Univ Calif Lawrence Livermore Natl Lab, Ctr Human Genome, Biol & Biotechnol Res Program, Livermore, CA 94550 USA
[4] Oak Ridge Natl Lab, Div Life Sci, Oak Ridge, TN 37831 USA
基金
美国能源部;
关键词
D O I
10.1023/A:1005533013926
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Molecular characterization of a novel gene designated Neuroendocrine-Specific Protein-Like-1 (Nspl1) had revealed that this gene is expressed as two transcripts, a 1.2 kb transcript found predominantly in skeletal muscle and a 2.1 kb transcript expressed in the brain. The exceptionally high level of skeletal muscle expression prompted us to determine where the protein is localized to skeletal muscle. In vitro studies were performed using two plasmid constructs that generate full-length Nspl1 muscle-specific protein fused to the green fluorescent protein (GFP). In one construct, the GFP cDNA was fused to the N-terminus of the Nspl1 cDNA while in the second construct, the GFP cDNA was fused to the C-terminus of the Nspl1 cDNA. Transfection of either plasmid into mononucleated myoblasts showed that the Nspl1-GFP chimeric protein was associated with intermediate filaments. This was confirmed by using an antibody to stain desmin and finding that GFP-Nspl1 colocalizes with desmin. Chick primary myoblasts were transfected with the chimeric cDNAs and allowed to differentiate into mature myotubes. Results from this analysis and the use of monoclonal antibody to stain alpha-actinin, further localized the Nspl1 protein to the Z-band of mature myotubes. Confocal microscopy of the myotubes containing Nspl1-GFP demonstrates that Nspl1 is distributed continuously throughout the Z-disks.
引用
收藏
页码:661 / 668
页数:8
相关论文
共 43 条
[1]   Analysis of skeletal and cardiac muscle from desmin knock-out and normal mice by high resolution separation of myosin heavy-chain isoforms [J].
Agbulut, O ;
Li, ZL ;
Mouly, V ;
ButlerBrowne, GS .
BIOLOGY OF THE CELL, 1996, 88 (03) :131-135
[2]   CHARACTERIZATION AND FIBER TYPE DISTRIBUTION OF A NEW MYOFIBRILLAR PROTEIN OF MOLECULAR-WEIGHT 32KDA [J].
CHEN, WYJ ;
DHOOT, GK ;
PERRY, SV .
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1986, 7 (06) :517-526
[3]   Use of green fluorescent protein variants to monitor gene transfer and expression in mammalian cells [J].
Cheng, LZ ;
Fu, J ;
Tsukamoto, A ;
Hawley, RG .
NATURE BIOTECHNOLOGY, 1996, 14 (05) :606-609
[4]   Myofibrillogenesis visualized in living embryonic cardiomyocytes [J].
Dabiri, GA ;
Turnacioglu, KK ;
Sanger, JM ;
Sanger, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9493-9498
[5]   COSTAMERES ARE SITES OF FORCE TRANSMISSION TO THE SUBSTRATUM IN ADULT-RAT CARDIOMYOCYTES [J].
DANOWSKI, BA ;
IMANAKAYOSHIDA, K ;
SANGER, JM ;
SANGER, JW .
JOURNAL OF CELL BIOLOGY, 1992, 118 (06) :1411-1420
[6]  
EMERSON CP, 1997, METHODS CELL BIOL, V52
[7]  
Engel A., 1994, MYOLOGY
[8]   Organization of protein and mRNA for titin and other myofibril components during myofibrillogenesis in cultured chicken skeletal muscle [J].
Fulton, AB ;
Alftine, C .
CELL STRUCTURE AND FUNCTION, 1997, 22 (01) :51-58
[9]   The importance of intermediate filaments in the adaptation of tissues to mechanical stress: Evidence from gene knockout studies [J].
Galou, M ;
Gao, J ;
Humbert, J ;
Mericskay, M ;
Li, ZL ;
Paulin, D ;
Vicart, P .
BIOLOGY OF THE CELL, 1997, 89 (02) :85-97
[10]   Molecular cloning of a novel mouse gene with predominant muscle and neural expression [J].
Geisler, JG ;
Stubbs, LJ ;
Wasserman, WW ;
Mucenski, ML .
MAMMALIAN GENOME, 1998, 9 (04) :274-282