Molecular Biology of the Cell click for CBE Life Science Education Page

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Turnacioglu, K. K.
Right arrow Articles by Sanger, J. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Turnacioglu, K. K.
Right arrow Articles by Sanger, J. W.

An N-terminal fragment of titin coupled to green fluorescent protein localizes to the Z-bands in living muscle cells: overexpression leads to myofibril disassembly

KK Turnacioglu, B Mittal, GA Dabiri, JM Sanger and JW Sanger

Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia 19104-6058, USA.

Cultures of nonmuscle cells, skeletal myotubes, and cardiomyocytes were transfected with a fusion construct (Z1.1GFP) consisting of a 1.1-kb cDNA (Z1.1) fragment from the Z-band region of titin linked to the cDNA for green fluorescent protein (GFP). The Z1.1 cDNA encodes only 362 amino acids of the approximately 2000 amino acids that make up the Z- band region of titin; nevertheless, the Z1.1GFP fusion protein targets the alpha-actinin-rich Z-bands of contracting myofibrils in vivo. This fluorescent fusion protein also localizes in the nascent and premyofibrils at the edges of spreading cardiomyocytes. Similarly, in transfected nonmuscle cells, the Z1.1GFP fusion protein localizes to the alpha-actinin-containing dense bodies of the stress fibers in vivo. A dominant negative phenotype was also observed in living cells expressing high levels of this Z1.1GFP fusion protein, with myofibril disassembly occurring as titin-GFP fragments accumulated. These data indicate that the Z-band region of titin plays an important role in maintaining and organizing the structure of the myofibril. The Z1.1 cDNA was derived from a chicken cardiac lambda gt11 expression library, screened with a zeugmatin antibody. Recent work has suggested that zeugmatin is actually part of the N-terminal region of the 81-kb titin cDNA. A reverse transcriptase polymerase chain reaction using a primer from the distal end (5' end) of the Z1.1 zeugmatin cDNA and a primer from the nearest known proximal (3' end) chicken titin (also called connectin) cDNA resulted in a predicted 0.3-kb polymerase chain reaction product linking the two known chicken titin cDNAs to each other. The linking region had a 79% identity at the amino acid level to human cardiac titin. This result and a Southern blot analysis of chicken genomic DNA hybridized with Z1.1 add further support to our original suggestion that zeugmatin is a proteolytic fragment from the N- terminal region of titin.

Volume 8, Issue 4, pp. 705-717, 04/01/1997
Copyright © 1997 by The American Society for Cell Biology




This article has been cited by other articles:


Home page
JCBHome page
C. Machado and D. J. Andrew
D-Titin: A Giant Protein with Dual Roles in Chromosomes and Muscles
J. Cell Biol., October 30, 2000; 151(3): 639 - 652.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
V Person, S Kostin, K Suzuki, S Labeit, and J Schaper
Antisense oligonucleotide experiments elucidate the essential role of titin in sarcomerogenesis in adult rat cardiomyocytes in long-term culture
J. Cell Sci., January 11, 2000; 113(21): 3851 - 3859.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
Y Zhang, D Featherstone, W Davis, E Rushton, and K Broadie
Drosophila D-titin is required for myoblast fusion and skeletal muscle striation
J. Cell Sci., January 9, 2000; 113(17): 3103 - 3115.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
P. van der Ven, J. Bartsch, M Gautel, H Jockusch, and D. Furst
A functional knock-out of titin results in defective myofibril assembly
J. Cell Sci., January 4, 2000; 113(8): 1405 - 1414.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
E Ehler, B. Rothen, S. Hammerle, M Komiyama, and J. Perriard
Myofibrillogenesis in the developing chicken heart: assembly of Z-disk, M-line and the thick filaments
J. Cell Sci., January 5, 1999; 112(10): 1529 - 1539.
[Abstract] [PDF]


Home page
JCBHome page
C. C. Gregorio, K. Trombitas, T. Centner, B. Kolmerer, G. Stier, K. Kunke, K. Suzuki, F. Obermayr, B. Herrmann, H. Granzier, et al.
The NH2 Terminus of Titin Spans the Z-Disc: Its Interaction with a Novel 19-kD Ligand (T-cap) Is Required for Sarcomeric Integrity
J. Cell Biol., November 16, 1998; 143(4): 1013 - 1027.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
C. Machado, C. E. Sunkel, and D. J. Andrew
Human Autoantibodies Reveal Titin as a Chromosomal Protein
J. Cell Biol., April 20, 1998; 141(2): 321 - 333.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
H. Aoki, S. Izumo, and J. Sadoshima
Angiotensin II Activates RhoA in Cardiac Myocytes : A Critical Role of RhoA in Angiotensin II–Induced Premyofibril Formation
Circ. Res., April 6, 1998; 82(6): 666 - 676.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. A. Dabiri, K. K. Turnacioglu, J. M. Sanger, and J. W. Sanger
Myofibrillogenesis visualized in living embryonic cardiomyocytes
PNAS, August 19, 1997; 94(17): 9493 - 9498.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]