期刊论文详细信息
Cell Division
Epitope of titin A-band-specific monoclonal antibody Tit1 5 H1.1 is highly conserved in several Fn3 domains of the titin molecule. Centriole staining in human, mouse and zebrafish cells
Erkki Juronen3  Imre Mikelsaar2  Anu Kõiveer3  Peeter Toomik1  Ruth Mikelsaar3  Alar Sünter3  Aavo-Valdur Mikelsaar2 
[1] Estonian University of Life Sciences, Tartu, Estonia;LabAs Ltd, Tartu, Estonia;Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
关键词: Zebrafish (Danio rerio);    Mouse;    Human being;    Evolution;    Fn3 domains;    Titin;   
Others  :  791079
DOI  :  10.1186/1747-1028-7-21
 received in 2012-03-14, accepted in 2012-09-14,  发布年份 2012
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【 摘 要 】

Background

Previously we have reported on the development of a new mouse anti-titin monoclonal antibody, named MAb Titl 5 H1.1, using the synthetic peptide N-AVNKYGIGEPLESDSVVAK-C which corresponds to an amino acid sequence in the A-region of the titin molecule as immunogen. In the human skeletal muscles, MAb Titl 5 H1.1 reacts specifically with titin in the A-band of the sarcomere and in different non-muscle cell types with nucleus and cytoplasm, including centrioles. In this report we have studied the evolutionary aspects of the binding of MAb Tit1 5 H1.1 with its target antigen (titin).

Results

We have specified the epitope area of MAb Tit1 5 H1.1 by subpeptide mapping to the hexapeptide N-AVNKYG-C. According to protein databases this amino acid sequence is located in the COOH-terminus of several different Fn3 domains of the A-region of titin molecule in many organisms, such as human being, mouse, rabbit, zebrafish (Danio rerio), and even in sea squirt (Ciona intestinalis). Our immunohisto- and cytochemical studies with MAb Tit1 5 H1.1 in human, mouse and zebrafish tissues and cell cultures showed a striated staining pattern in muscle cells and also staining of centrioles, cytoplasm and nuclei in non-muscle cells.

Conclusions

The data confirm that titin can play, in addition to the known roles in striated muscle cells also an important role in non-muscle cells as a centriole associated protein. This phenomenon is highly conserved in the evolution and is related to Fn3 domains of the titin molecule. Using titin A-band-specific monoclonal antibody MAb Tit1 5 H1.1 it was possible to locate titin in the sarcomeres of skeletal muscle cells and in the centrioles, cytoplasm and nuclei of non-muscle cells in phylogenetically so distant organisms as Homo sapiens, Mus musculus and zebrafish (Danio rerio).

【 授权许可】

   
2012 Mikelsaar et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Mikelsaar AV, Sünter A, Toomik P, Mikelsaar R, Kalev I, Kõiveer A, Piirsoo A, Karpson K, Juronen E: Titin a-band-specific monoclonal antibody Tit1 5 H1.1. cellular titin as a centriolar protein in non-muscle cells. Hybridoma 2010, 29:391-401.
  • [2]Kumar S, Hedges SB: A molecular timescale for vertebrate evolution. Nature 1998, 392:917-920.
  • [3]Bromham L, Phillips MJ, Penny D: Growing up with dinosaurs: molecular dates and the mammalian radiation. Trends Ecol Evol 1999, 14:113-118.
  • [4]Bromham L, Penny D, Rambaut A, Hendy MD: The power of relative rates tests depends on the data. J Mol Evol 2000, 50:296-301.
  • [5]Postlethwait JH, Woods IG, Ngo-Hazelett P, Yan YL, Kelly PD, Chu F, Huang H, Hill-Force A, Talbot WS: Zebrafish comparative genomics and the origins of vertebrate chromosomes. Genome Res 2000, 10:1890-1902.
  • [6]Woods IG, Kelly PD, Chu F, Ngo-Hazelett P, Yan YL, Huang H, Postlethwait JH, Talbot WS: A comparative map of the zebrafish genome. Genome Res 2000, 10(12):1903-1914.
  • [7]Liu TX, Zhou Y, Kanki JP, Deng M, Rhodes J, Yang HW, Sheng XM, Zon LI, Look AT: Evolutionary conservation of zebrafish linkage group 14 with frequently deleted regions of human chromosome 5 in myeloid malignancies. PNAS 2002, 99:6136-6141.
  • [8]Hedges SB, Blair JE, Venturi ML, Shoe JL: A molecular timescale of eukaryote evolution and the rise of complex multicellular life. BMC Evol Biol 2004, 4:2. BioMed Central Full Text
  • [9]Benton MJ, Donoghue PCJ: Paleontological Evidence to Date the Tree of Life. Mol Biol Evol 2007, 24:26-53.
  • [10]Costa ML, Roberta C, Escaleira RC, Rodrigues VB, Manasfi M, Mermelstein CS: Some distinctive features of zebrafish myogenesis based on unexpected distributions of the muscle cytoskeletal proteins actin, myosin, desmin, α-actinin,troponin and titin. Mech Dev 2002, 116:95-104.
  • [11]Muhle-Goll C, Pastore A, Nilges M: The three-dimensional structure of a type I module from titin: a prototype of intracellular fibronectin type III domains. Structure 1998, 6:1291-1302.
  • [12]Muhle-Goll C, Habeek M, Cazorla O, Nilges M, Labeit S, Granzier H: Structural and evolutional studies of titin’s fn3 modules reveal conserved surface pattems and binding to myosin Sl-a possible role in the Frank-Starling mechanism of the heart. J Mol Biol 2001, 313:431-447.
  • [13]Labeit S, Kolmerer B: Titins: giant proteins in charge of muscle ultrastructure and elasticity. Science 1995, 270:293-295.
  • [14]Kenny PA, Liston EM, Higgins DG: Molecular evolution of immunoglobulin and fibronectin domains in titin and related muscle proteins. Gene 1999, 232:11-23.
  • [15]Amodeo P, Fraternali F, Lesk AM, Pastore A: Modularity and homology: modelling of the titin type I modules and their interfaces. J Mol Biol 2001, 311:283-296.
  • [16]Head JG, Houmeida A, Knight P, Clarke AR, Trinick J, Brady RL: Stability and folding rates of domains spanning the large A-band super-repeat of titin. Biophys J 2001, 81:1570-1579.
  • [17]Tskhovrebova L, Trinick J: Properties of titin immunoglobulin and fibronectin-3 domains. J Biol Chem 2004, 279:46351-46354.
  • [18]Tskhovrebova L, Trinick J: Roles of titin in the structure and elasticity of the sarcomere. J Biomed Biotechnol 2010.
  • [19]Labeit S, Gautel M, Lakey A, Trinick J: Towards a molecular understanding of titin. EMBO J 1992, 11:1711-1716.
  • [20]Soteriou A, Gamage M, Trinick J: A survey of interactions made by the giant muscle protein titin. J Cell Sci 1993, 104:119-123.
  • [21]Houmeida A, Holt J, Tskhovrebova L, Trinick J: Studies of the interaction between titin and myosin. J Cell Biol 1995, 131:1471-1481.
  • [22]Espreafico EM, Coling DE, Tsakraklides V, Krogh K, Wolenski JS, Kalinec G, Kachar B: Localization of myosin-V in the centrosome. Proc Natl Acad Sci USA 1998, 95:8636-8641.
  • [23]Andersen JS, Wilkinson CJ, Mayor T, Mortensen P, Erich A, Nigg EA, Mann M: Proteomic characterization of the human centrosome by protein correlation profiling. Nature 2003, 426:570-574.
  • [24]Zastrow MS, Flaherty DB, Benian GM, Wilson KL: Nuclear titin interacts with A- and B-type lamins in vitro and in vivo. J Cell Sci 2005, 119:239-249.
  • [25]Gupta T, Mullins MC: Dissection of organs from the adult zebrafish. J Vis Exp 2010, (37):e1717.
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