Dysfunctions of the translational machinery in digestive glands of mussels exposed to mercury ions

Aquatic Toxicology

Volumn 134-135, Issue , 2013, Pages 23-33

  Pytharopoulou, Sofia ^a   Kournoutou, Georgia G ^a   Leotsinidis, Michel ^a   Georgiou, Christos D ^b   Kalpaxis, Dimitrios L ^a  

^a UNIVERSITY OF PATRAS   (Greece)

^b UNIVERSITY OF PATRAS   (Greece)

Author keywords

Mercury; Mussels; Oxidative stress; ROS; Translation

Indexed keywords

MERCURY; PEPTIDYLTRANSFERASE; SUPEROXIDE DISMUTASE; TRANSFER RNA;

BIOSPHERE; DIGESTIVE SYSTEM; GENOTOXICITY; ION; MERCURY (ELEMENT); MOLLUSC; PEPTIDE; POLLUTION EXPOSURE; PROTEIN; RNA;

AMINOACYLATION; ANIMAL EXPERIMENT; ARTICLE; BINDING SITE; BIOACCUMULATION; COMPLEX FORMATION; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; ENZYME ACTIVITY; EXOCRINE GLAND; LIPID PEROXIDATION; MERCURIALISM; MICRONUCLEUS TEST; MUSSEL; NONHUMAN; OXIDATION REDUCTION STATE; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN SYNTHESIS INHIBITION; RNA TRANSLATION; RNA TRANSPORT;

ANIMALS; BIOLOGICAL MARKERS; BIVALVIA; DIGESTIVE SYSTEM; EXOCRINE GLANDS; GILLS; LIPID PEROXIDATION; MERCURY; MICRONUCLEUS TESTS; OXIDATIVE STRESS; PROTEIN BIOSYNTHESIS; RIBOSOME SUBUNITS; SUPEROXIDE DISMUTASE; WATER POLLUTANTS, CHEMICAL;

MYTILUS GALLOPROVINCIALIS;

EID: 84875659779     PISSN: 0166445X     EISSN: 18791514     Source Type: Journal    
DOI: 10.1016/j.aquatox.2013.02.014     Document Type: Article

References (59)

1. Agusa T., Kunito T., Sudaryanto A., Monirith I., Kan-Atireklap S., Iwata H., Ismail A., Sanguansin J., Muchtar M., Tana T.S., Tanabe S. Exposure assessment for trace elements from consumption of marine fish in Southeast Asia. Environmental Pollution 2007, 145:766-777.
2. Amarantos I., Xaplanteri M.A., Choli-Papadopoulou T., Kalpaxis D.L. Effects of two photoreactive spermine analogues on peptide bond formation and their application for labeling proteins in Escherichia coli functional ribosomal complexes. Biochemistry 2001, 40:7641-7650.
3. Amarantos I., Zarkadis I.K., Kalpaxis D.L. The identification of spermine binding sites in 16S rRNA allows interpretation of the spermine effect on ribosomal 30S subunit functions. Nucleic Acids Research 2002, 30:2832-2843.
4. Annicchiarico C., Biandolino F., Cardellicchio N., Di Leo A., Giandomenico S., Prato E. Predicting toxicity in marine sediment in Taranto Gulf (Ionian Sea Southern Italy) using sediment quality guidelines and a battery bioassay. Ecotoxicology 2006, 16:239-246.
5. Avery S.V. Molecular targets of oxidative stress. Biochemical Journal 2011, 434:201-210.
6. Bailly M., Giannouli S., Blaise M., Stathopoulos C., Kern D., Becker H.D. A single tRNA base pair mediates bacterial tRNA-dependent biosynthesis of asparagine. Nucleic Acids Research 2006, 34:6083-6094.
7. Baird C., Cann M. Environmental Chemistry 2004, W.H. Freeman, New York.
8. Bradford M.M. A rapid and sensitive method for quantification of microgram quantities of protein, utilizing the principle of protein-dye binding. Analytical Biochemistry 1976, 72:248-254.
9. Bolognesi C., Fenech M. Mussel micronucleus cytome assay. Nature Protocols 2012, 7:1125-1137.
10. Bond U. Stressed out! Effects of environmental stress on mRNA metabolism. FEMS Yeast Research 2006, 6:160-170.
11. Boujbiha M.A., Ben Salah G., Ben Feleh A., Saoudi M., Kamoun H., Bousslema A., Ommezzine A., Said K., Fakhfakh F., El Feki A. Hematotoxicity and genotoxicity of mercuric chloride following sub-chronic exposure through drinking water in male rats. Biological Trace Element Research 2012, 148:76-82.
12. Budkevich T.V., El'skaya A.V., Nierhaus K.H. Features of 80S mammalian ribosome and its subunits. Nucleic Acids Research 2008, 36:4736-4744.
13. Calabro A.R., Gazarian D.I., Barile F.A. Effect of metals on β-actin and total protein synthesis in cultured human intestinal epithelial cells. Journal of Pharmacological and Toxicological Methods 2011, 63:47-58.
14. Carrasco L., Diez S., Soto D.X., Catalan J., Bayona J.M. Assessment of mercury and methylmercury pollution with zebra mussel (Dreissena polymorpha) in the Ebro River (NE Spain) impacted by industrial hazardous dumps. Science of the Total Environment 2008, 407:178-184.
15. Caskey C.T., Beaudet A.L., Tate W.P. Mammalian release factor; in vitro assay and purification. Methods in Enzymology 1974, 30:293-303.
16. Ciesiołka J., Michałowski Wrzesinski J., Krajewski J., Krzyzosiak W.J. Patterns of cleavages induced by lead ions in defined RNA secondary structure motifs. Journal of Molecular Biology 1998, 275:211-220.
17. Cohen S.S. A Guide to Polyamines 1998, Oxford University Press, New York.
18. Cully M., Downward J. Translational responses to growth factors and stress. Biochemical Society Transactions 2009, 37:284-288.
19. De Flora S., Bennicelli C., Bagnasco M. Genotoxicity of mercury compounds. A Review. Mutation Research 1994, 317:57-79.
20. Ehrenstein C., Shu P., Wickenheiser E.B., Hirner A.V., Dolfen M., Emons H., Obe G. Methyl mercury uptake and associations with the induction of chromosomal aberrations in Chinese hamster ovary (CHO) cells. Chemico-Biological Interactions 2002, 141:259-274.
21. Farina M., Avila D.S., da Rocha J.B.T., Aschner M. Metals, oxidative stress and neurodegeneration: A focus on iron, manganese and mercury. Neurochemistry International 2012, doi:pii: S0197-0186(12)00396-8. 10.1016/j.neuint.2012.12.006.
22. Ferreras A.C., Bandeira E., Cayama E., Zambrano R., Avila H., Yépez A., Triana J.L., Triana-Alonso F.J. Efficient and faithful in vitro translation of natural and synthetic mRNA with human ribosomes. International Journal of Molecular Medicine 2004, 13:527-536.
23. Franco R., Sánchez-Olea R., Reyes-Reyes E.M., Panayiotidis M. Environmental toxicity, oxidative stress and apoptosis. Ménage à Trois. Mutation Research 2009, 674:3-22.
24. Freimann P., Schmidt D. Determination of mercury in seawater by cold vapour atomic absorption specto-photometry. Analytical and Bioanalytical Chemistry 1984, 317:792.
25. Georgiou C.D., Papapostolou I., Patsoukis N., Tsegenidis T., Sideris T. An ultrasensitive fluorescent assay for the in vivo quantification of superoxide radical in organisms. Analytical Biochemistry 2005, 347:144-151.
26. Gochfeld M. Cases of mercury exposure, bioavailability, and absorption. Ecotoxicology and Environmental Safety 2003, 56:174-179.
27. Grant C.M. Regulation of translation by hydrogen peroxide. Antioxidants and Redox Signalling 2011, 15:191-203.
28. Hardt W.D., Schlegl J., Erdmann V.A., Hartmann R.K. Role of the D arm and the anticodon arm in tRNA recognition by eubacterial and eukaryotic RNase P enzymes. Biochemistry 1993, 32:13046-13053.
29. Holcik M., Sonenberg N. Translational control in stress and apoptosis. Nature Reviews Molecular Cell Biology 2005, 6:318-327.
30. Ivanković D., Pavicić J., Erk M., Filipović-Marijić V., Raspor B. Evaluation of the Mytilus galloprovincialis Lam. digestive gland metallothionein as a biomarker in a long-term field study: seasonal and spatial variability. Marine Pollution Bulletin 2005, 50:1303-1313.
31. Ivanov L., Lesauskaité V., Ivanoviené L., Sadauskiené I., Gaileviĉiûté R., Karĉiauskait D., Rodoviĉius H. Effects of cadmium ions on the initial stage of translation and the cell death in mouse liver. Medicina 2005, 41:47-53.
32. Jackson R.J., Hellen C.U., Pestova T.V. The mechanism of eukaryotic translation initiation and principles of its regulation. Nature Reviews Molecular Cell Biology 2010, 11:113-127.
33. Ji X., Wang W., Cheng J., Yuan T., Zhao X., Zhuang H., Qu L. Free radicals and antioxidant status in rat liver after dietary exposure of environmental mercury. Environmental Toxicology and Pharmacology 2006, 22:309-314.
34. Kalpaxis D.L., Drainas D. Effect of spermine on peptide-bond formation, catalyzed by ribosomal peptidyltransferase. Molecular and Cellular Biochemistry 1992, 115:19-26.
35. Kalpaxis D.L., Amarantos I., Tsibouxi A., Papapetropoulou M. Regulation of translation initiation in mussels (Mytilus galloprovincialis, lam.) following contamination stress. Journal of Toxicology and Environmental Health. Part A 2003, 14:481-494.
36. Kaul G., Pattan G., Rafeequi T. Eukaryotic elongation factor-2 (eEF2): its regulation and peptide chain elongation. Cell Biochemistry and Function 2011, 29:227-234.
37. Klaholz B.P. Molecular recognition and catalysis in translation termination complexes. Trends in Biochemical Sciences 2011, 36:282-292.
38. Korencić D., Söll D., Ambrogelly A. A one-step method for in vitro production of tRNA transcripts. Nucleic Acids Research 2002, 30:e105.
39. Liu M., Gong X., Alluri R.K., Wu J., Sablo T., Li Z. Characterization of RNA damage under oxidative stress in Escherichia coli. Biological Chemistry 2012, 393:123-132.
40. Marshall R.A., Aitken C.E., Dorywalska M., Puglisi J.D. Translation at the single-molecule level. Annual Review of Biochemistry 2008, 77:177-203.
41. Miller D.M., Lund B.O., Woods J.S. Reactivity of Hg(II) with superoxide: evidence for the catalytic dismutation of superoxide by Hg(II). Journal of Biochemical Toxicology 1991, 6:293-298.
42. Murayama A., Raffin J.P., Remy P., Ebel J.P. Yeast phenylalanyl-tRNA synthetase: properties of the sulfhydryl groups; evidence for -SH requirement in tRNA acylation. FEBS Letters 1975, 53:15-22.
43. Phe in ternary complex with EF-Tu:GTP. Biochemistry and Molecular Biology International 1993, 31:95-103.
44. Petropoulos A.D., Xaplanteri M.A., Dinos G.P., Wilson D.N., Kalpaxis D.L. Polyamines affect diversely the antibiotic potency: insight gained from kinetic studies of the blasticidin S and spiramycin interactions with functional ribosomes. Journal of Biological Chemistry 2004, 279:26518-26525.
45. Pytharopoulou S., Sazakli E., Grintzalis K., Georgiou C.D., Leotsinidis M., Kalpaxis D.L. Translational responses of Mytilus galloprovincialis to environmental pollution: integrating the responses to oxidative stress and other biomarker responses into a general stress index. Aquatic Toxicology 2008, 89:18-27.
46. Pytharopoulou S., Grintzalis K., Sazakli E., Leotsinidis M., Georgiou C.D., Kalpaxis D.L. Translational responses and oxidative stress of mussels experimentally exposed to Hg, Cu and Cd: one pattern does not fit at all. Aquatic Toxicology 2011, 105:157-165.
47. Raftopoulou E.K., Dimitriadis V.K. Comparative study of the accumulation and detoxification of Cu (essential metal) and Hg (nonessential metal) in the digestive gland and gills of mussels Mytilus galloprovincialis, using analytical and histochemical techniques. Chemosphere 2011, 83:1155-1165.
48. Rodovičius H., VieŽelienè D., Stavenevičienè I., Sadauskienè I., KaŠauskas A., Ivanov L. Effects of lead ions on activities of tRNALeu and leucyl-tRNA synthetase of mouse liver. Medicina 2003, 39:683-688.
49. Schurz F., Sabater-Vilar M., Fink-Gremmels J. Mutagenicity of mercury chloride and mechanisms of cellular defense: the role of metal-binding proteins. Mutagenesis 2000, 15:525-530.
50. Saikia M., Krokowski D., Bo-Jhih G., Ivanov P., Parisien M., Hu G., Anderson P., Pan T., Hatzoglou M. Genome-wide identification and quantitative analysis of cleaved tRNA fragments induced by cellular stress. Journal of Biological Chemistry 2012, 285:42708-42725.
51. Stien X., Percic P., Gnassia-Barelli M., Roméo M., Laufaurie M. Evaluation of biomarkers in caged fishes and mussels to assess the quality of waters in a bay of the NW Mediterranean Sea. Environmental Pollution 1998, 99:339-345.
52. Syversen T.L. Effects of methyl mercury on protein synthesis in vitro. Acta Pharmacologica et Toxicologica (Copenh) 1981, 49:422-426.
53. Regoli F., Benedetti M., Giuliani M.E. Antioxidant defenses and acquisition of tolerance to chemical stress. Tolerance to Environmental Contaminants 2011, 153-173. CRC Press, Boca Raton, FL. C. Amiard-Triquet, P.S. Rainbow, M. Roméo (Eds.).
54. Thompson D.M., Lu C., Green P.J., Parker R. tRNA cleavage is a conserved response to oxidative stress in eukaryotes. RNA 2008, 14:2095-2103.
55. Tyedmers J., Madariaga M.L., Lindquist S. Prion switching in response to environmental stress. PLoS Biology 2008, 6:e294.
56. Viarengo A., Ponzano E., Dondero F., Fabbri R. A simple spectrophotometric method for metallothionein evaluation in marine organisms: an application to Mediterranean and Antarctic mollusks. Marine Environment Research 1997, 44:69-84.
57. Xie L., Flippin J.L., Deighton N., Funk D.H., Dickey D.A., Buchwalter D.B. Mercury(II) bioaccumulation and antioxidant physiology in four aquatic insects. Environmental Science & Technology 2009, 43:934-940.
58. Yamasaki S., Anderson P. Reprogramming mRNA translation during stress. Current Opinion in Cell Biology 2008, 20:222-226.
59. Zamora R., Alaiz M., Hidalgo F.J. Feed-back inhibition of oxidative stress by oxidized lipid/amino acid reaction products. Biochemistry 1997, 36:15765-15771.