ZHANG Jian-She, XIA Xin-Jie, CHU Wu-Ying, CHEN Ding-Gen, FU Gui-Hong, LIU Zhen, CHENG Jia, LIU Fang, LU Shuang-Qing. GENE EXPRESSI ON PROFI LES OF THEM USCLE TISSUES OF THEMANDARIN FISH,SIN IPERCA CHUATSI L. W ITH ZEBRAFISH cDNA M ICROARRAY[J]. ACTA HYDROBIOLOGICA SINICA, 2009, 33(1): 46-53.
Citation: ZHANG Jian-She, XIA Xin-Jie, CHU Wu-Ying, CHEN Ding-Gen, FU Gui-Hong, LIU Zhen, CHENG Jia, LIU Fang, LU Shuang-Qing. GENE EXPRESSI ON PROFI LES OF THEM USCLE TISSUES OF THEMANDARIN FISH,SIN IPERCA CHUATSI L. W ITH ZEBRAFISH cDNA M ICROARRAY[J]. ACTA HYDROBIOLOGICA SINICA, 2009, 33(1): 46-53.

GENE EXPRESSI ON PROFI LES OF THEM USCLE TISSUES OF THEMANDARIN FISH,SIN IPERCA CHUATSI L. W ITH ZEBRAFISH cDNA M ICROARRAY

  • Received Date: May 12, 2008
  • Rev Recd Date: November 22, 2008
  • Published Date: January 24, 2009
  • The mandarin fish has been recently becoming one of the most important aquaculture fish species in China be-cause of its good meat quality and protein composition1I mproving the production of these fish is a continuing goal of the aq-uaculture industry, and a better understanding of the molecular control of the muscle structure and development in this commercially important species could prove beneficial for more economic rearing and quality of production1Therefore,we intended to investigate what genes control the development of large amount of high-quality white muscle in this species, which may provide foundation for the understanding of itsmyogensis and information to refine musculature for aquaculture1 cDNA microarray is a powerful tool for the assaying of an organism’ s gemone and expression profiles1However, it is relatively behind in fish because limited arrays available1In order to obtain the gene expression profile and screen differ-entially expressed genes in muscle tissues in themandarin fish,we applied theAffymetrix zebrafish cDNA microarray heter-olously hybridized to both themadarin fish, Siniperca chuatsi and the silver carp, H1molitrix1Total RNAswere isolated from the muscle tissues of the two species of fish and labeled with biotin, and hybridized to Zebrafish cDNA gene chips1Hybridized microarray chips were scanned with Affymetrix 418 Array Scanner1All expression signals from the hy-bridization to 156.7 genes in zebrafish cDNA array were analyzed by R/Bioconductor software (http://www1bioconductor1org) 1Background correction and normalization were done by the methods of Robust multi-Array Aver-age known as gcRMA in R/Bioconductor1Out of 15617 genes in Zebrafish cDNA chips, total of 375 geneswere identified to be significantly expressed in themuscle tissuesof the two fishes1Compared to the silver carp, 180 genes are up-regulated and 195 are down-regulated in the madarine fish’ smuscle tissues1Among the 180 up-regulated genes, 49 genes are func-tionally known and 131 are unknown1The 49 known genes could be categorized into seven functional groups and several of them are considered aspotential candidates related to the fish’ smuscle structure and development1Several genes related to the muscle structure and meat textureswere identified, including myosin heavy chain gene (MYH),myofiber linker gene (plectin) and cytoskeletal structure genes (tubulin and actin) 1In themandarin fish,myosin heavy chain gene is expressed extremely higher at 3-% than that in the silver carp (Tab1-) and this large amount ofmyosin heavy chain protein expres-sion may reflect to the large abundance of high-qualitywhite muscle in this fish1Plactin identified from mammalian muscle tissue is another gene directly related to muscle structure and it functions as a cytolinker to cytoskeletal proteins and signal transductor1Plactin was expressed 16.5% higher in the mandarin fish than that in silver carp (log-ratio at 3195/3130). Titin gene was also highly expressed in both of the two fish1These results indicated that the muscle tissue of the mandarin fish was highly endurant and elastic1A cluster of genes functioning in cytoskeleton and dynamics including tubulin iso-forms, actin and microtubule-associated protein genes were quite abundantly expressed in the muscle of the mandarin fish1This group of genes played important roles in muscle cell structure, cell division and material transportation1In com-parison to the silver carp, both alpha-and beta-tubulin were expressed at 21% and 17% higher in themandarin fish,which suggested that high amount of tubulin protein in muscle cells of the mandarin fish may be directly related to itsmuscle e-lastic feature1 This is the first study using zebrafish cDNA microarray to heterogonous hybridization of other evolutionally far from fish species, and this information can be used to help select strains of high quality ofmuscular species for aquaculture industry and to provide a better understanding of gene expression profiles in relation to their biological functions in muscle tissue of different fish species.
  • [1]
    Douglas S E. Microarray studies of gene expression in fish[J]. Om ics, 2006, 10: 474-489
    [2]
    Sherlock G. Of fish and chips[J]. Nat M ethods, 2005, 2: 329-330
    [3]
    Ton C, Stamatiou D, Liew C C. Gene expression profile of zebrafish exposed to hypoxia during development [J]. Physiol Genom ics, 2003, 13: 97-106
    [4]
    Linney E, DobbsMcAuliffe B, Sajadi H, et al. Microarray gene expression profiling during the segmentation phase of zebrafish development [J]. Comp B iochem Physiol C Toxicol Phar macol, 2004, 138: 351-362
    [5]
    Yamasaki Y, Komoike Y, Higashinakagawa T. Adaptive changes in TEF1 gene expression during cold acclimation in the medaka [J]. Zoolog Sci, 2006, 23: 903-908
    [6]
    Adams A, Thompson K D. Biotechnology offers revolution to fish health management[J]. Trends B iotechnol, 2006, 24: 201-205
    [7]
    Lam S H,Wu YL,Vega V B, et al. Conservation of gene expression signatures between zebrafish and human liver tumors and tumor progression[J]. Nat B iotechnol, 2006, 24: 73-75
    [8]
    Martin S A, Blaney S C, Houlihan D F. Transcriptome response following administration of a live bacterial vaccine in Atlantic salmon (Salmo salar) [J]. Mol Immunol, 2006, 43: 1900-1911
    [9]
    Byon J Y,Ohira T, Hirono I, et al. Use of a cDNA microarray to study immunity against viral hemorrhagic septicemia (VHS) in Japanese flounder (Paralichthysolivaceus) followingDNA vaccination[J]. Fish Shellfish Immunol, 2005, 18: 135-147
    [10]
    Tsoi S C, Cale J M,Bird IM, et al. Use of human cDNA microarrays for identification of differentially expressed genes in Atlantic salmon liver during Aeromonas salmonicida infection [J]. M ar B iotechnol(NY), 2003, 5: 545-554
    [11]
    W irgin I, Waldman J R. Resistance to contaminants in North American fish populations[J]. M utat Res, 2004, 552: 73-100
    [12]
    Koskinen H, Pehkonen P,Vehniainen E, et al. Response of rainbow trout transcriptome to model chemical contaminants[J]. B iochem B iophys Res Commun, 2004, 320: 745-753
    [13]
    Tang J Z, Zhang D Y, Chen J, et al. Comparative analysis of the amino acid composition and profemic patterns of the muscle proteins from teleostes, S. chuatsi and H. M olitrix [J]. Journal of Fisheries of China, 2007, 31 (3): 361-368
    [14]
    Bolstad B M, Irizaarry,AstrandM, et al. A comparison of nor malization methods for high density oligonucleotide array data based on bias and variance[J]. B ioinfor matics, 2003, 19: 185-193
    [15]
    Wu Z. A model2based background adjustment for oligonucleotide expression arrays[J]. J. Am. Atat. Assoc., 2004, 99: 909-917
    [16]
    Renn S C,AubinHorth N, Hofmann H A. Biologicallymeaningful expression profiling across species using heterologous hybridization to a cDNA microarray[J]. BMC Genom ics, 2004, 5: 42
    [17]
    Gauvry L, Fauconneau B. Cloning of a trout fast skeletal myosin heavy chain expressed both in embryo and adult muscles and in myotubes neoformed in vitro[J]. Comp B iochem Physiol B B iochem Mol B iol, 1996, 115: 183-190
    [18]
    Guo X F, Nakaya M,Watabe S. Myosin subfragment1 isoforms having different heavy chain structures from fast skeletal muscle of thermally acclimated carp[J]. J B iochem (Tokyo), 1994, 116: 728-735
    [19]
    BoczonadiV,McInroyL,Maatta A. Cytolinker cross2talk: periplakin N2ter minus interactswith plactin to regulate keratin organization and epithelialmigration[J]. Exp Cell Res,2007,313(16):3579-3591
    [20]
    Dugina V, Fontao L, Chaponnier C, et al. Focal adhesion features duringmyofibroblastic differentiation are controlled by intracellular and extracellular factors[J]. J Cell Sci, 2001, 114: 3285-3296
    [21]
    Fontao L, Geerts D, Kuikman I, et al. The interaction of plectin with actin: evidence for cross2linkingof actin filaments by dimerization of the actin2binding domain of plectin [J]. J Cell Sci, 2001, 114: 2065-2076
    [22]
    Rezniczek G A, Konieczny P,Nikolic B. Plactin If scaffolding at the sarcolemma of dystrophic (mda) muscle fibers throughmultiple interaction with beta2dystroglycan[J]. Cell B iol,. 2007, 176 (7): 965-977
    [23]
    Dumont E, Ralliere C, Tabet K C, et al. A NLRR1 gene is expressed inmigrating slow muscle cellsof the trout (Oncorhynchus mykiss) eemryos[J]. Dev Genes Evol, 2007, 217(6): 469-475
    [24]
    Kudo H, Amizuka N, Araki K, et al. Zebrafish periostin is required for the adhesion ofmuscle fiber bundles to the myoseptum and for the differentiation of the muscle fibers[J]. Dev B iol, 2004, 267 (2): 473-487
    [25]
    Cortes F,Daggett D,BrysonRichardson R J, et al. Cadherinmediated differential cell adhesion controls slow muscle cell migration in the developing zebrafish myotome[J]. Dev Cell, 2003, 5 (6): 865-876
    [26]
    Wade R H. Microtubules: an overview [J]. M ethods M ol Med, 2007, 137: 1-16
    [27]
    Ebner H L, CordasA, Pafundo D E, et al. I mportance of cytoskeletal elements in volume regulatory responses of trout hepatocytes [J]. Am J Physiol Regul Integr Comp Physiol, 2005, 289: R877-890
    [28]
    Modig C, RutbergM,Detrich H W. MAP 0, a 4002kDa microtubule2associated protein unique to teleost fish[J]. Cell Motil Cytoskeleton, 1997, 38: 258-269
    [29]
    Detrich H W,NeighborsB W, Sloboda R D. Microtubule-associated proteins from Antarctic fishes[J]. Cell M otil Cytoskeleton, 1990, 17: 174-186
    [30]
    Nilsson H, RutbergM,WallinM. Localization of kinesin and cytoplasmic dynein in cultured melanophores from Atlantic cod, Gadusmorhua[J]. CellM otil Cytoskeleton, 1996, 33: 183-196
    [31]
    Nguyen V, Joly J,Bourrat F. An in situ screen for genes controlling cell proliferation in the optic tectum of the medaka (Oryzias latipes) [J]. M ech Dev, 2001, 107: 55-67
    [32]
    Ikegami R, RiveraBennettsA K,BrookerD L, et al. Effect of inhibitors ofDNA replication on early zebrafish embryos: evidence for coordinate activation of multiple intrinsic cell2cycle checkpoints at the mid2blastula transition[J]. Zygote, 1997, 5: 153-175
    [33]
    McLean L, Young I S,DohertyM K. Global cooling: cold acclimation and the expression of soluble proteins in carp skeletal muscle[J]. Proteom ics, 2007, 7: 2667-2681
    [34]
    Ng C E,Osato M, Tay B H, et al. cDNA cloning of Runx family genes from the pufferfish (Fugu rubripes) [J]. Gene, 2007, 399: 162-173
    [35]
    Kausel G, SalazarM,CastroL, et al. Modular changesof cis2regulatory elements from two functional Pit 1 genes in the duplicated genome of Cyprinus carpio[J]. J Cell B iochem, 2006,99: 905-921
    [36]
    Evenhuis J, Bengten E, Snell C, et al. Characterization of additional novel immune type receptors in channel catfish, Ictalurus punctatus[J]. Immunogenetics, 2007, 59: 661-671
    [37]
    Watzke J, Schir mer K, Scholz S. Bacterial lipopolysaccharides induce genes involved in the innate immune response in embryos of the zebrafish (Danio rerio) [J]. Fish Shellfish Immunol, 2007, 23: 901-905
    [38]
    Bei J X, Zhang Y,LiW S, et al. Application of genome databases and bioinformatics in exploration for fish genes[J]. Acta Hydrobiologica Sinica, 2008, 32(3): 387-392[贝锦新,张勇,李文笙, 等. 鱼类基因数据库与生物信息学在鱼类基因开发上的应 用. 水生生物学报, 2008, 3(3): 387-392]
    [39]
    Zhao H B, Peng K,Wang Y F, et al. Progress of studies on myostatin in fish[J]. Acta Hydrobiologica Sinica, 2006, 3 (2): 227-231[赵浩斌,彭扣,王玉凤,等. 鱼类生长抑制素 (myostatin) 研究进展. 水生生物学报, 2006, 3(2): 227-231]
    [40]
    Li X M, Fan W, Zhang B, et al. Cloning of myostatin of common carp (Cyprinus carpio) and its expression pattern in different tissues [J]. Acta Hydrobiologica Sinica, 2007, 31 (5): 643-648 [李兴美,范巍,张彬,等.鲤鱼肌肉生长抑制基因 (MSTN)的 克隆及其组织表达特征. 水生生物学报, 2007, 31 (5): 643-648]
  • Cited by

    Periodical cited type(16)

    1. 贾濮元,郭华阳,朱克诚,刘宝锁,郭梁,张楠,江世贵,张殿昌. 黄鳍棘鲷精子冷冻保存方法探究. 南方水产科学. 2021(06): 58-65 .
    2. 刘光霞,吴兴兵,何勇凤,邓智明,杨德国,王小明,杨少荣,刘欢. 圆口铜鱼精子超低温冷冻保存. 中国水产科学. 2020(01): 44-52 .
    3. 马林,李楠,郝爽,吴会民,姜巨峰,刘克明,白晓慧,刘肖莲,李春艳,尤宏争. 乌克兰鳞鲤精子超低温冷冻保存方法研究. 水产科学. 2019(04): 473-478 .
    4. 王鑫伟,史应学,魏平,竺俊全,吴雄飞. 乙二醇降低超低温冷冻黄姑鱼精子的DNA损伤. 动物学杂志. 2016(02): 261-267 .
    5. 王肇霖,陈睿毅,楼宝,詹炜,徐冬冬,王立改,刘峰. 小黄鱼精液超低温冷冻保存技术的试验研究. 浙江海洋学院学报(自然科学版). 2016(01): 15-18 .
    6. 史应学,程顺,竺俊全,吴雄飞. 中国花鲈精子的超低温冷冻保存及酶活性检测. 水生生物学报. 2015(06): 1241-1247 . 本站查看
    7. 杨春玲,赵永贞,彭敏,陈晓汉,李咏梅,陈秀荔. 单细胞凝胶电泳检测南美白对虾冷冻精子的DNA损伤. 动物医学进展. 2014(09): 58-62 .
    8. 韩龙江,刘清华,于道德,官曙光,纪利芹,王文琪,刘名,温海深,李军. 太平洋鳕(Gadus macrocephalus)精液超低温冷冻方法的建立及精子超微结构分析. 海洋与湖沼. 2014(04): 789-797 .
    9. 张艺. 大黄鱼精子冷冻保存方法的研究. 宁德师范学院学报(自然科学版). 2014(03): 225-228+234 .
    10. 程顺,闫家强,竺俊全,姜建湖,吴雄飞,史会来. 大黄鱼(Pseudosciaena crocea)精子冷冻前后的活力及超微结构变化. 海洋与湖沼. 2013(01): 56-61 .
    11. 李霞,刘志丹,秦艳杰. 中间球海胆精子超低温冷冻损伤的研究. 大连海洋大学学报. 2012(02): 105-109 .
    12. 芦春斌,杨冬宇,高忱,刘标. 转基因大豆对雄性鼠生殖系统的安全性评估. 扬州大学学报(农业与生命科学版). 2012(01): 23-27 .
    13. 吴兴华,郑凌凌,宋立荣. 渗透与非渗透性抗冻剂联用技术对铜绿微囊藻的超低温保藏研究. 水生生物学报. 2012(02): 344-351 . 本站查看
    14. 姜建湖,闫家强,竺俊全,杨万喜. 大黄鱼精子的超低温冻存及细胞结构损伤的检测. 农业生物技术学报. 2011(04): 725-733 .
    15. 金春华,闫家强,竺俊全. 黄姑鱼精子的超低温冻存及细胞结构损伤的检测. 水产学报. 2011(06): 846-853 .
    16. 骆新荣,马瑛,孟浩,高庆华. 奶牛性控与常规冻精DNA损伤的彗星检测. 中国奶牛. 2011(20): 6-8 .

    Other cited types(9)

Catalog

    Article views (870) PDF downloads (638) Cited by(25)
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return