Muscle growth and muscle function: A molecular biological perspective

被引:26
作者
Goldspink, G
机构
[1] Dept. of Anat. and Devmtl. Biology, Royal Free Hospital, University of London, London NW3 2PF, Rowland Hill Street
基金
英国惠康基金;
关键词
D O I
10.1016/S0034-5288(96)90038-7
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Molecular biological methods are pervading all biomedical fields and it is likely that they will soon introduce new techniques to veterinary diagnostics and have a major impact on food and fibre production in animal agriculture. The ability to manipulate muscle growth and phenotype will present new ethical problems, particularly if the techniques are used to manipulate muscle development in greyhounds and racehorses where the financial rewards could be very substantial. Muscle has been a useful tissue for the study of the molecular control of tissue development because terminal differentiation results in the production of large quantities of highly specialised proteins. Now that the functional anatomy of structural genes in muscle is being elucidated, a coherent picture is beginning to emerge of the way in which post-natal muscle growth and phenotype are regulated at the gene level. The hormones and growth factors involved in regulating the quantitative and qualitative changes in gene expression are now better understood, together with the ability of the tissue to adapt to physical signals and hence new activity patterns. The myosin heavy chain isoform genes which encode the myosin cross-bridges (the force generators for muscular contraction) exist as a large multigene family. The contractility and other characteristics of muscle depend to a large extent on the differential expression of members of this and other gene families. Muscle fibres adapt for increased power output by expressing a subset of 'fast' genes and for increased economy of action by expressing a slow subset of genes and producing more mitochondria. With the increasing understanding of gene expression in muscle, there are prospects for manipulating the mass, contractility and other characteristics of muscle and also to change its phenotype and understand certain disease states.
引用
收藏
页码:193 / 204
页数:12
相关论文
共 100 条
[1]  
ALEXANDER M, 1977, MECH ENERGETICS ANIM, P1
[3]   INTRICATE COMBINATORIAL PATTERNS OF EXON SPLICING GENERATE MULTIPLE REGULATED TROPONIN-T ISOFORMS FROM A SINGLE GENE [J].
BREITBART, RE ;
NGUYEN, HT ;
MEDFORD, RM ;
DESTREE, AT ;
MAHDAVI, V ;
NADALGINARD, B .
CELL, 1985, 41 (01) :67-82
[4]   IDENTIFICATION OF A MYOCYTE NUCLEAR FACTOR THAT BINDS TO THE MUSCLE-SPECIFIC ENHANCER OF THE MOUSE MUSCLE CREATINE-KINASE GENE [J].
BUSKIN, JN ;
HAUSCHKA, SD .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (06) :2627-2640
[5]   MYOSIN ISOZYME TRANSITIONS OCCURRING DURING THE POSTNATAL-DEVELOPMENT OF THE RAT SOLEUS MUSCLE [J].
BUTLERBROWNE, GS ;
WHALEN, RG .
DEVELOPMENTAL BIOLOGY, 1984, 102 (02) :324-334
[6]  
CHANG KC, 1995, J CELL SCI, V108, P1779
[7]  
CHANG KC, 1993, J CELL SCI, V106, P331
[8]  
CHENEY R E, 1992, Current Opinion in Cell Biology, V4, P27, DOI 10.1016/0955-0674(92)90055-H
[9]   SKELETAL-MUSCLE EXPRESSION AND ABNORMAL FUNCTION OF BETA-MYOSIN IN HYPERTROPHIC CARDIOMYOPATHY [J].
CUDA, G ;
FANANAPAZIR, L ;
ZHU, WS ;
SELLERS, JR ;
EPSTEIN, ND .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2861-2865