Myosin heavy chain genes expressed in juvenile and adult silver carp Hypopthalmichthys molitrix: Novel fast-type myosin heavy chain genes of silver carp

被引:17
作者
Fukushima, Hideto [1 ]
Ikeda, Daisuke [1 ]
Tao, Yan [2 ]
Watabe, Shugo [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Aquat Mol Biol & Biotechnol, Bunkyo Ku, Tokyo 1138657, Japan
[2] Shanghai Ocean Univ, Coll Food Sci & Technol, Shanghai 200090, Peoples R China
基金
日本学术振兴会;
关键词
cDNA cloning; Fast skeletal muscle; Phylogenetic tree; Slow skeletal muscle; FAST SKELETAL-MUSCLE; MYOFIBRILLAR ATPASE; SUBFRAGMENT-1; ISOFORMS; REGION; SUBSTITUTIONS; ADAPTATIONS; CLONING; WHITE; RED;
D O I
10.1016/j.gene.2008.11.022
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Silver carp Hypopthalmichthys molitrix is eurythermal temperate fish, whose muscle is considered to express several types of myosin heavy chain (MYH) genes at different stages of its growth and to adjust to the environmental temperature. In this study, MYH genes expressed in the muscles of juvenile and adult silver carp were investigated. Five types of MYH cDNA clone were isolated from silver carp (H. molitrix) by RACE strategy using a set of fast-type MYH specific primers, and termed scMYH(F1), scMYH(F2), scMYH(F3), scMYH(F4) and scMYH(F5) in the order of their abundance in cDNA libraries constructed from fast skeletal muscles of adult silver carp. scMYH(F1), scMYH(F3) and scMYH(F5) showed high nucleotide sequence identities of 96, 98 and 96% to gcMYH(F30), gcMYH(F10) and gcMYH(F1), respectively, that encode MYHs predominantly expressed in fast skeletal muscle of grass carp (Ctenopharyngodon idella) acclimated to 30, 10 and 20 degrees C, respectively. scMYH(F2) and scMYH(F4) showed a high identity to A4-type MYH from rock cod (Notothenia coriiceps) slow skeletal muscle. Phylogenetic analysis demonstrated that scMYH(F1), and scMYH(F5) were monophyletic with fish adult fast-type MYHs, whereas scMYH(F2) and scMYH(F4) formed a cluster with fish slow-like fast-type MYH, and scMYH(F3) did with fish embryonic fast-type MYHs. Interestingly, juvenile silver carp predominantly expressed scMYH(F3) irrespective of acclimation temperatures at 10, 18 or 26 degrees C. The comparison among scMYH(F1), scMYH(F2) and scMYH(F3) in the deduced amino acid sequence revealed that the putative binding sites for ATP, actin, and essential and regulatory light chains in myosin subfragment-1 (S1) have high identities with each other (81-100%). However, their loop-1 and loop-2 regions in S1 were highly variable, suggesting their different functions. The deduced amino acid sequences of myosin subfragment-2 and L-meromyosin showed high identities of 90-91% and 86-90%, respectively, among the above three scMYHs. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:102 / 111
页数:10
相关论文
共 39 条
[1]   THE COVALENT MALEIMIDOBENZOYL-ACTIN-MYOSIN HEAD COMPLEX - CROSS-LINKING OF THE 50 KDA HEAVY-CHAIN REGION TO ACTIN SUBDOMAIN-2 [J].
BERTRAND, R ;
DERANCOURT, J ;
KASSAB, R .
FEBS LETTERS, 1994, 345 (2-3) :113-119
[2]  
BOBKOV AA, 1996, P NATL ACAD SCI USA, V81, P1991
[3]   PHYLOGENETIC ANALYSIS OF THE MYOSIN SUPERFAMILY [J].
CHENEY, RE ;
RILEY, MA ;
MOOSEKER, MS .
CELL MOTILITY AND THE CYTOSKELETON, 1993, 24 (04) :215-223
[4]   A conserved C-terminal assembly region in paramyosin and myosin rods [J].
Cohen, C ;
Parry, DAD .
JOURNAL OF STRUCTURAL BIOLOGY, 1998, 122 (1-2) :180-187
[5]   New insights into myosin evolution and classification [J].
Foth, BJ ;
Goedecke, MC ;
Soldati, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (10) :3681-3686
[6]   Characterisation of red and white muscle myosin heavy chain gene coding sequences from antarctic and tropical fish [J].
Gauvry, L ;
Ennion, S ;
Ettelaie, C ;
Goldspink, G .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2000, 127 (04) :575-588
[7]   Selective gene expression during adaptation of muscle in response to different physiological demands [J].
Goldspink, G .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1998, 120 (01) :5-15
[8]   MYOSIN SUBFRAGMENT-1 ISOFORMS HAVING DIFFERENT HEAVY-CHAIN STRUCTURES FROM FAST SKELETAL-MUSCLE OF THERMALLY ACCLIMATED CARP [J].
GUO, XF ;
NAKAYA, M ;
WATABE, S .
JOURNAL OF BIOCHEMISTRY, 1994, 116 (04) :728-735
[9]   CONSEQUENCES OF THERMAL-CHANGE ON THE MYOFIBRILLAR ATPASE OF 5 FRESH-WATER TELEOSTS [J].
HEAP, SP ;
WATT, PW ;
GOLDSPINK, G .
JOURNAL OF FISH BIOLOGY, 1985, 26 (06) :733-738
[10]   Structure-function relationships of the two surface loops of myosin heavy chain isoforms from thermally acclimated carp [J].
Hirayama, Y ;
Sutoh, K ;
Watabe, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 269 (01) :237-241