|
|
||||||||
AJP - Cell Physiology, Vol 262, Issue 1 C1-C8, Copyright © 1992 by American Physiological Society
ARTICLES |
B. Russell and D. J. Dix
Department of Physiology, University of Illinois, Chicago 60680.
The intracellular distribution of mRNA in striated muscle fibers is highly ordered, as is the structural organization of the fibers' contractile apparatus. Results from in situ hybridization of muscle mRNA are reviewed in an attempt to discern the mechanisms involved in mRNA distribution and to determine its relationship to developmental, growth, and repair processes in muscle. Nonradioactively labeled complementary RNA probes allow anatomic localization of mRNA at the light and electron microscopic level. Myosin mRNA in striated muscle is concentrated around transcriptionally active nuclei, myosin mRNA is excluded by the myofibrillar mass, myosin mRNA distribution correlates with that of cytoskeletal elements, and myosin mRNA is concentrated in regions of rapid growth and repair. The even distribution of myosin mRNA along the length of myofibrils gives no indication of specific association with either the thick or thin filaments. Of the possible mechanisms directing mRNA distribution, results from in situ hybridization and other analyses support a restricted diffusion model. Diffusion of mRNA (and polysomes) is severely limited by the myofibrillar lattice. It is possible that myosin mRNA is also associated with a cytoskeletal element, which may direct the mRNA to specific intracellular locations and affect translational activity.
This article has been cited by other articles:
![]() |
D. Scholz, C. F. Baicu, W. J. Tuxworth, L. Xu, H. Kasiganesan, D. R. Menick, and G. Cooper IV Microtubule-dependent distribution of mRNA in adult cardiocytes Am J Physiol Heart Circ Physiol, March 1, 2008; 294(3): H1135 - H1144. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Fluck, C. Dapp, S. Schmutz, E. Wit, and H. Hoppeler Transcriptional profiling of tissue plasticity: role of shifts in gene expression and technical limitations J Appl Physiol, August 1, 2005; 99(2): 397 - 413. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Russell, D. Motlagh, and W. W. Ashley Form follows function: how muscle shape is regulated by work J Appl Physiol, March 1, 2000; 88(3): 1127 - 1132. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. R. Roy, S. R. Monke, D. L. Allen, and V. R. Edgerton Modulation of myonuclear number in functionally overloaded and exercised rat plantaris fibers J Appl Physiol, August 1, 1999; 87(2): 634 - 642. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Nikcevic, M. C. Heidkamp, M. Perhonen, and B. Russell Mechanical activity in heart regulates translation of alpha -myosin heavy chain mRNA but not its localization Am J Physiol Heart Circ Physiol, June 1, 1999; 276(6): H2013 - H2019. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. C. Dolber, R. P. Bauman, J. C. Rembert, and J. C. Greenfield Jr. Are interatrial band myocytes maximally hypertrophied in normal canine hearts? Am J Physiol Heart Circ Physiol, October 1, 1998; 275(4): H1225 - H1235. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. L. Nakhoul, B. A. Davis, M. F. Romero, and W. F. Boron Effect of expressing the water channel aquaporin-1 on the CO2 permeability of Xenopus oocytes Am J Physiol Cell Physiol, February 1, 1998; 274(2): C543 - C548. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |