Temperature and the expression of seven muscle-specific protein genes during embryogenesis in the Atlantic cod Gadus morhua L.

被引:32
作者
Hall, TE
Cole, NJ
Johnston, IA
机构
[1] Univ St Andrews, Gatty Marine Lab, Sch Biol, St Andrews KY16 8LB, Fife, Scotland
[2] Univ Dundee, Div Cell & Dev Biol, Dundee DD1 5EH, Scotland
关键词
Gadus morhua; temperature; development; muscle; in situ hybridization; cod; myofibril; MyoD; myosin; troponin; creatine kinase;
D O I
10.1242/jeb.00535
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Seven cDNA clones coding for different muscle-specific proteins (MSPs) were isolated from the fast muscle tissue of Atlantic cod Gadus morhua L. In situ hybridization using cRNA probes was used to characterize the temporal and spatial patterns of gene expression with respect to somite stage in embryos incubated at 4degreesC, 7degreesC and 10degreesC. MyoD transcripts were first observed in the presomitic mesoderm prior to somite formation, and in the lateral compartment of the forming somites. MyoD expression was not observed in the adaxial cells that give rise to the slow muscle layer, and expression was undetectable by in situ hybridization in the lateral somitic mesoderm after the 35-somite stage, during development of the final similar to15 somites. RT-PCR analysis, however, confirmed the presence of low levels of the transcript during these later stages. A phylogenetic comparison of the deduced amino-acid sequences of the full-length MyoD cDNA clone and those from other teleosts, and inference from the in situ expression pattern suggested homology with a second paralogue (MyoD2) recently isolated from the gilthead seabream Sparus aurata. Following MyoD expression, alpha-actin was the first structural gene to be switched on at the 16-somite stage, followed by myosin heavy chain, troponin T, troponin I and muscle creatine kinase. The final mRNA in the series to be expressed was troponin C. All genes were switched on prior to myofibril assembly. The troponin C sequence was unusual in that it showed the greatest sequence identity with the rainbow trout Oncorhynchus mykiss cardiac/slow form, but was expressed in the fast myotomal muscle and not in the heart. In addition, the third TUC calcium binding site showed a lower level of sequence conservation than the rest of the sequence. No differences were seen in the timing of appearance or rate of posterior progression (relative to somite stage) of any MSP transcripts between embryos raised at the different temperatures. It was concluded that myofibrillar genes are activated asynchronously in a distinct temporal order prior to myofibrillar assembly and that this process was highly canalized over the temperature range studied.
引用
收藏
页码:3187 / 3200
页数:14
相关论文
共 108 条
[1]  
Allendorf F.W., 1984, P1
[2]   An application of the annual egg production method to estimate the spawning biomass of cod (Gadus morhua L.), plaice (Pleuronectes platessa L.) and sole (Solea solea L.) in the Irish Sea [J].
Armstrong, MJ ;
Connolly, P ;
Nash, RDM ;
Pawson, MG ;
Alesworth, E ;
Coulahan, PJ ;
Dickey-Collas, M ;
Milligan, SP ;
O'Neill, MF ;
Witthames, PR ;
Woolner, L .
ICES JOURNAL OF MARINE SCIENCE, 2001, 58 (01) :183-203
[3]   Male reproductive competition in spawning aggregations of cod (Gadus morhua, L.) [J].
Bekkevold, D ;
Hansen, MM ;
Loeschcke, V .
MOLECULAR ECOLOGY, 2002, 11 (01) :91-102
[4]  
BENFIELD PA, 1984, J BIOL CHEM, V259, P4979
[5]   Physiologically regulated alternative splicing patterns of fast troponin T RNA are conserved in mammals [J].
Briggs, MM ;
Schachat, F .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (01) :C298-C305
[6]  
BROOKS S, 1993, MAR BIOL, V117, P501
[7]   WHITE MUSCLE DIFFERENTIATION IN THE EEL (ANGUILLA-ANGUILLA L) - CHANGES IN THE MYOSIN ISOFORMS PATTERN AND ATPASE PROFILE DURING POST-METAMORPHIC DEVELOPMENT [J].
CHANOINE, C ;
GUYOTLENFANT, M ;
ELATTARI, A ;
SAADI, A ;
GALLIEN, CL .
DIFFERENTIATION, 1992, 49 (02) :69-75
[8]  
Chenchik A, 1998, RT PCR METHODS GENE, P305
[9]   Some distinctive features of zebrafish myogenesis based on unexpected distributions of the muscle cytoskeletal proteins actin, myosin, desmin, α-actinin, troponin and titin [J].
Costa, ML ;
Escaleira, RC ;
Rodrigues, VB ;
Manasfi, M ;
Mermelstein, CS .
MECHANISMS OF DEVELOPMENT, 2002, 116 (1-2) :95-104
[10]   DEVELOPMENTAL-CHANGES IN THE COMPOSITION OF MYOFIBRILLAR PROTEINS IN THE SWIMMING MUSCLES OF ATLANTIC HERRING, CLUPEA-HARENGUS [J].
CROCKFORD, T ;
JOHNSTON, IA .
MARINE BIOLOGY, 1993, 115 (01) :15-22