Zhang, Y., Tan, X., Xu, P. et al. Quantitative comparison of the expression of myogenic regulatory factors in flounder (Paralichthys olivaceus) embryos and adult tissues., Chin. J. Ocean. Limnol. 28, 248–253 (2010). https://doi.org/10.1007/s00343-010-9286-9
DOI:
Zhang, Y., Tan, X., Xu, P. et al. Quantitative comparison of the expression of myogenic regulatory factors in flounder (Paralichthys olivaceus) embryos and adult tissues., Chin. J. Ocean. Limnol. 28, 248–253 (2010). https://doi.org/10.1007/s00343-010-9286-9DOI:
Quantitative comparison of the expression of myogenic regulatory factors in flounder (Paralichthys olivaceus) embryos and adult tissues
摘要
Abstract
MyoD
Myf5
and myogenin are myogenic regulatory factors that play important roles during myogenesis. It is thought that MyoD and Myf5 are required for myogenic determination
while myogenin is important for terminal differentiation and lineage maintenance. To better understand the function of myogenic regulatory factors in muscle development of flounder
an important economic fish in Asia
real-time quantitative RT-PCR was used to characterize the expression patterns of MyoD
Myf5
and myogenin at early stages of embryo development
and in different tissues of the adult flounder. The results show that
Myf5 is the first gene to be expressed during the early stages of flounder development
followed by MyoD and myogenin. The expressions of Myf5
yoD
and myogenin at the early stages have a common characteristic: expression gradually increased to a peak level
and then gradually decreased to an extremely low level. In the adult flounder
the expression of the three genes in muscle is much higher than that in other tissues
indicating that they are important for muscle growth and maintenance of grown fish. During embryonic stages
the expression level of MyoD might serve an important role in the balance between muscle cell differentiation and proliferation. When the MyoD expression is over 30% of its highest level
the muscle cells enter the differentiation stage.
关键词
Keywords
references
Berkes C. Tapscott, S. 2005. MyoD and the transcriptional control of myogenesis. Cell Dev. Biol., 16: 585–595.
Chen L, Krause M, Sepanski M, Fire A. 1994. The Caenorhabditis elegans MyoD homologue HLH-1 is essential for proper muscle function and complete morphogenesis. Development, 120: 1 631–1 641.
Chen Y H, Lee W C, Liu C F, Tsai H J. 2001. Molecular structure, dynamic expression, and promoter analysis of zebrafish (Danio rerio) myf-5 gene. Genesis, 29: 22–35.
Edmonson D G, Olson E N. 1993. Helix-loop-helix proteins as regulators of muscle-specific transcription. J. Biol. Chem., 268: 755–758.
Gu W, Schneider J W, Condorelly G, Kaushal S, Mahdavi V, Nadal-Ginard B. 1993. Interaction of myogenic factors and the retinoblastoma protein mediates muscle cell commitment and differentiation. Cell, 72: 309–324.
Hammond C L, Hinits Y, Osborn D P, Minchin J E, Tettamanti G, Hughes S M. 2007. Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish. Dev. Biol., 302(2): 504–521.
Hinits Y, Osborn D P, Hughes S M. 2009. Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations. Development, 136(3): 403–414.
Kassar-Duchossoy L, Gayraud-Morel B, Gomes D, Rocancourt D, Buckingham M, Shinin V, Tajbakhsh S. 2004. Mrf4 determines skeletal muscle identity in Myf5:Myod double-mutant mice. Nature, 431: 466–471.
Kitzmann M, Fernandez A. 2001. Crosstalk between cell cycle regulators and the myogenic factor MyoD in skeletal myoblasts. Cell. Mol. Life Sci., 58: 571–579.
Lyons G E, Buckingham M E. 1992. Developmental regulation of myogenesis in the mouse. Semin. Dev. Biol., 3: 243–253.
Megeney L, Rudnicki M A. 1995. Determination versus differentiation and the MyoD family of transcription factors. Biochem. Cell Biol., 73: 723–732.
Ott M O, Bober E, Lyons G, Arnold H H, Buckingham M. 1991. Early expression of the myogenic regulatory gene, Myf-5, in precursor cells of skeletal muscle in the mouse embryo. Development, 111: 1 097–1 107.
Parker M H, Seale P, Rudnicki M A. 2003. Looking back to the embryo: defining transcriptional networks in adult myogenesis. Nat. Rev. Genet., 4: 497–507.
Paterson B M, Walldorf U, Eldridge J, Dübendorfer A, Frasch M, Gehring W J. 1991. The Drosophila homologue of vertebrate myogenic-determination genes encodes a transiently expressed nuclear protein marking primary myogenic cells. Proc. Natl. Acad. Sci. USA, 88: 3 782–3 786.
Reynaud E G, Leibovitch M P, Tintignac L A, Pelpel K, Guillier M, Leibovitch S A. 2000. Stabilization of MyoD by direct binding to p57 (Kip2). J. Biol. Chem., 275: 18 767–18 776.
Rowlerson A, Veggetti A. 2001. Cellular mechanisms of post-embryonic muscle growth in aquaculture species. In: Johnston I A ed. Muscle Development and Growth. Fish Physiol., vol. 18, pp. 103–140.
Rudnicki M A, Jaenisch R. 1995. The MyoD family of transcription factors and skeletal myogenesis. BioEssays, 17: 203–209.
Rudnicki M A, Schnegelsberg P N, Stead R H, Braun T, Arnold H H, Jaenisch R. 1993. MyoD or Myf-5 is required for the formation of skeletal muscle. Cell, 75: 1 351–1 359.
Sassoon D, Eyons G, Wright, W E, Lin V, Lassar A, Weintraub H, Buckingham M. 1989. Expression of two myogenic regulatory factors myogenin and MyoD1 during mouse embryogenesis. Nature, 341: 303–307.
Tan X, Zhang Y, Zhang P J, Xu P, Xu Y. 2006. Molecular structure and expression patterns of flounder (Paralichthys olivaceus) Myf-5, a myogenic regulatory factor. Comp. Biochem. Physiol. B., 145: 204–213.
Wei Q, Paterson B M. 2001. Regulation of MyoD function in the dividing myoblasts. FEBS., 490: 171–178.
Weinberg E S, Allende M L, Kelly C S, Aboulmagd A, Murakami T, Andermann P, Doerre O G, Grunwald D J, Riggleman B. 1996. Developmental regulation of zebrafish MyoD in wild-type, no tail and spadetail embryos. Development, 122: 271–280.
Xu P, Tan X, Zhang Y, Zhang P J, Xu Y. 2007. Cloning and expression analysis of myogenin from flounder (Paralichthys olivaceus) and promoter analysis of muscle-specific expression. Comp. Biochem. Physiol. B., 147: 135–145.
Zhang J M, Wei Q, Zhao X, Paterson B M. 1999a. Coupling of the cell cycle and myogenesis through the cyclin D1-dependent interaction of MyoD with cdk4. EMBO. J., 18: 926–933.
Zhang J M, Zhao X, Wei Q, Paterson B M. 1999b. Direct inhibition of G1 cdk kinase activity by MyoD promotes myoblast cell cycle withdrawal and terminal differentiation. EMBO. J., 18: 6 983–6 993.
Zhang Y, Tan X, Zhang P J, Xu Y. 2006. Characterization of muscle regulatory gene, MyoD, from flounder (Paralichthys olivaceus) and analysis of its expression patterns during embryogenesis. Mar. Biotechnol. (NY), 8: 139–148.
The trial reading is over, you can activate your VIP account to continue reading.
Effect of fasting on protein metabolism in muscle tissue of Larimichthys crocea revealed by transcriptome and proteome
Identification and profiling of microRNAs of Euphausia superba using Illumina deep sequencing
Screening of eye-position related genes with DD-RT-PCR and RDA in the hybrids between Japanese flounder Paralichthys olivaceus and stone flounder Kareius bicoloratus
Further observation of the spermatozoa of lefteye flounderParalichthys olivaceus by electronic microscopy
Carbon budget of bastard halibutParalichthys olivaceus in relation to body weight and temperature
Related Author
Yu ZHANG
Weiliang SHEN
Juan LI
Baoxiao ZHENG
Zhengjia LOU
Mohammad Aslam HOSAIN
Baoying QIAN
Liangyi XUE
Related Institution
Ningbo Institute of Marine and Fisheries
School of Life Science, Taizhou University
College of Marine Sciences, Ningbo University
Key Laboratory of Oceanic and Polar Fisheries, Ministry of Agriculture, East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences
Key Laboratory of East China Sea Fishery Resources Exploitation, Ministry of Agriculture, East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences