Expression of genes responsible for biomineralization of Pinctada fucata during development

Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology

Volumn 155, Issue 3, 2010, Pages 241-248

  Miyazaki, Yoko ^a   Nishida, Takuma ^a   Aoki, Hideo ^b   Samata, Tetsuro ^a  

^a AZABU UNIVERSITY   (Japan)

^b Mie Prefecture Fisheries Research Institute   (Japan)

Author keywords

Crystal polymorphism; Gene expression; Ontogeny; Pinctada fucata; Real time polymerase chain reaction (PCR); Scanning electron microscopy (SEM); Shell microstructure; X ray diffraction

Indexed keywords

BETA ACTIN; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE; RNA 18S;

ARTICLE; BIOMINERALIZATION; CONTROLLED STUDY; DEVELOPMENTAL STAGE; GENE EXPRESSION; GENE FUNCTION; GROWTH RATE; HOUSEKEEPING GENE; LARVA; LARVAL DEVELOPMENT; LARVAL SHELL; MINERALOGY; NONHUMAN; NUCLEOTIDE SEQUENCE; ONTOGENY; PINCTADA; PINCTADA FUCATA; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION;

PINCTADA FUCATA;

EID: 74649083667     PISSN: 10964959     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbpb.2009.11.009     Document Type: Article

References (46)

1. Awaji M. Separation of outer epithelial cells from pearl oyster mantle by deispase digestion. In: Fraser M.J. (Ed). Eighth International Conference on Invertebrate and Fish Tissue Culture (1991), Tissue Culture Association. Press, California 43-46
2. Awaji M., and Machii A. A method for separation of outer epithelial cells from pearl oyster (Pinctada fucata martensii) mantle. Tissue Cult Res Commun 8 (1989) 89
3. Bayane B.L. Growth and the delay of metamorphosis of the larvae of Mytilus edulis (L). Ophelia 2 (1965) 1-47
4. Beniash E., Aizenberg J., Addadi L., and Weiner S. Amorphous calcium carbonate transforms into calcite during sea urchin larval spicule growth. Proc. R. Soc. Lond., B 264 (1997) 461-465
5. Cariolou M.A., and Morse D.E. Purification and characterization of calcium-binding conchiolin shell peptides from the mollusk, Haliotis rufescens, as a function of development. J. Comp. Physiol. B 157 (1988) 717-729
6. Crenshaw M.A. The soluble matrix from Mercenaria mercenaria shell. Biomineralization 6 (1972) 6-11
7. Fujimura T., Wada K., and Iwaki T. Development and morphology of the pearl oyster larvae, Pinctada fucata. Venus 54 (1995) 25-48
8. George N.C., Kikkian C.E., and Wilt F.H. Characterization and expression of a gene encoding a 30.6-kDa Strongylocentrotus purpuratus spicule matrix protein. Dev. Biol. 147 (1991) 334-342
9. Greenfield E.M., Wilson D.C., and Crenshaw M.A. Ionotropic nucleation of calcium carbonate by molluscan matrix. Am. Zool. 24 (1984) 925-932
10. Hasse B., Ehrenberg H., Marxen J.C., Becker W., and Epple M. Calcium carbonate modificsations in the mineralized shell of the freshwater snail Biomphalaria glabrata. Chem. Eur. J. 6 (2000) 3679-3685
11. Jacob D.E., Soldati A.L., Wirth R., Huth J., Wehrmeister U., and Hofmeister W. Nanostructure, Composition and mechanisms of bivalve shell growth. Geochim. Cosmochim. Acta 72 (2008) 5401-5415
12. Kobayashi I. Various patterns of biomineralization and its phylogenetic significances in bivalve molluscs. In: Omori M., and Watabe N. (Eds). The Mechanisms of Biomineralization in Animals and Plants (1980), Tokai Univ. Press, Tokyo 145-155
13. Kobayashi I. Function of hard tissues for cementation in bibalbes. In: Wada K., and Kobayashi I. (Eds). Biomineralization and Hard Tissue of Marine Organisms (1996), Tokai Univ. Press, Tokyo 205-218
14. Kobayashi I., and Samata T. Bivalve shell structure and organic matrix. Mater. Sci. Eng. C-Bio. S. 26 (2006) 692-698
15. Koga K., Hara A., and Akune S. Correlation of nucleolytic activities with the stage of growth of the silkworm. J. Insect Physiol. 15 (1969) 799-806
16. Livingston B.T., Killian C.E., Wilt F.H., Cameron A., Landrum M.J., Ermolaeva O., Sapojnikov V., Maglott D.R., Buchanan A.M., and Ettensohn C.A. A genome-wide analysis of biomineralization-related proteins in the sea urchin Strongylocentrotus purpuratus. Dev. Biol. 300 (2006) 335-348
17. Mao C.L., Golubic S., Le C.T., and Payri C. Developmental aspects of biomineralization in the Polynesian pearl oyster Pinctada margaritifera var. cumingii. Oceanol. Acta 24 (2001) S37-S49
18. Marin F., Luquet G., Marie B., and Medakovic D. Molluscan shell proteins: primary structure, origin, and evolution. Curr. Top. Dev. Biol. 80 (2008) 209-275
19. Medakovic D. Carbonic anhydrase activity and biomineralization process in embryos, larvae and adult blue mussels Mytilus edulis L. Helbol. Mar. Res. 54 (2000) 1-6
20. Miyamoto H., Miyashita T., Okushima M., Nakano S., Morita T., and Matsushiro A. A carbonic anhydrase from the nacreous layer in oyster pearls. Proc. Natl. Acad. Sci. USA 93 (1996) 9657-9660
21. Miyamoto H., Miyoshi F., and Kohno J. The carbonic anhydrase domain protein nacrein is expressed in the epithelial cells of the mantle and acts as a negative regulator in calcification in the mollusk Pinctada fucata. Zool. Sci. 22 (2005) 311-315
22. Miyazaki Y., Usui T., Kajikawa A., Hishiyama H., Matsuzawa N., Nishida T., Machii A., and Samata T. Daily oscillation of gene expression associated with nacreous layer formation. Front. Mater. Sci. China 2 2 (2008) 162-166
23. Nassif N., Pinna N., Gehrke N., Antonietti M., Jäger C., and Cölfen H. Amorphous layer around aragonite platelets in nacre. Proc. Natl. Acad. Sci. USA 102 (2005) 12653-12655
24. Norizuki M., and Samata T. Distribution and function of the nacrein-related protein inferred from structural analysis. Mar. Biotechnol. 10 (2008) 234-241
25. Okabe K., Koyanagi R., and Koga K. RNA in the degenerating silk gland of Bombyx mori. J. Insect Physiol. 21 6 (1975) 1305-1309
26. 3 crystallization. Cryst. Eng. Comm. 9 (2007) 1171-1177
27. Samata T., Hayashi N., and Kono M. A new matrix protein family related to the nacreous layer formation of Pinctada fucata. FEBS Lett. 462 (1999) 225-229
28. Schönitzer V., and Weiss I.M. The structure of mollusc larval shells formed in the presence of the chitin synthase inhibitor Nikkomycin Z. BMC Struct. Biol. 7 71 (2007) 1-24
29. Sudo S., Fujikawa T., Nagakura T., Ohkubo T., Sakaguchi K., Tanaka M., Nagashima K., and Takahashi T. Structure of mollusk shell framework proteins. Nature 387 (1997) 563-564
30. Suzuki M., and Nagasawa H. The structure-function relationship analysis of Prismalin-14 from the prismatic layer of the Japanese pearl oyster, Pinctada fucata. FEBS J. 274 (2007) 5158-5166
31. Suzuki M., Murayama E., Inoue H., Ozaki N., Tohse H., Kogure T., and Nagasawa H. Characterization of Prismalin-14, a novel matrix protein from the prismatic layer of the Japanese peal oyster (Pinctada fucata). Biochem. J. 382 (2004) 205-213
32. Suzuki M., Sakuda S., and Nagasawa H. Identification of chitin in the prismatic layer of the shell and a chitin synthase gene from the Japanese pearl oyster, Pinctada fucata. Biosci. Biotechnol. Biochem. 71 (2007) 1735-1744
33. Suzuki M., Saruwatari K., Kogure T., Yamamoto Y., Nishimura T., Kato T., and Magasawa H. An aidic mtrix potein, Pif, is a key macromolecule for nacre formation. Science 325 5946 (2009) 1388-1390
34. Takakura D., Norizuki M., Ishikawa F., and Samata T. Isolation and characterization of the N-linked oligosaccharides in nacrein from Pinctada fucata. Mar. Biotechnol. 10 (2008) 290-296
35. Takeuchi T., and Endo K. Biphasic and dually coordinated expression of the genes encoding major shell matrix proteins in the pearl oyster Pinctada fucata. Mar. Biotechnol. 8 (2006) 52-61
36. Taylor J.D., Kennedy W.J., and Hall A. The shell structure and mineralogy of the bivalvia. Introduction. nuculacea-trigonacea. Bull. Br. Mus. (Nat. Hist.) 3 (1969) 1-125
37. Tsukamoto D., Sarashina I., and Endo K. Structure and expression of an unusual acidic matrix protein of pearl oyster shells. Biochem. Biophys. Res. Commun. 320 (2004) 1175-1180
38. Uozumi S., and Suzuki S. The evolution of shell structures in the bivalvia. In: Habe T., and Omori M. (Eds). Study of Molluscan Paleobiology (1981), Kokusai Press Inc. 63-78
39. Watabe N. In: Trueman E.R., and Clarke M.R. (Eds). Shell Structure. The Mollusca vol.11 (1988), Academic Press Inc. 289-316
40. Weiner S. Aspartic acid-rich proteins: major components of the soluble organic matrix mollusk shells. Calcif. Tissue Int. 29 (1979) 163-167
41. Weiss I.M., and Schönitzer V. The distribution of chitin in larval shells of the bivalve mollusk Mytilus galloprovincialis. J. Struct. Biol. 153 (2006) 264-277
42. Weiss I.M., Tuross N., Addadi L., and Weiner S. Mollusc larval shell formation: amorphous calcium carbonate is a precursor phase for aragonite. J. Exp. Zool. 293 (2002) 478-491
43. Weiss I.M., Nitzer V., Eichner N., and Sumper M. The chitin synthase involved in marine bivalve mollusk shell formation contains a myosin domain. FEBS Lett. 580 (2006) 1846-1852
44. Wilt F.H. Developmental biology meets materials science: morphogenesis of biomineralized structures. Dev. Biol. 280 (2005) 15-25
45. Wilt F.H., Killian C.E., and Livingston B.T. Development of calcareous skeletal elements in invertebrates. Differentiation 71 (2003) 237-250
46. Yano M., Nagai K., Morimoto K., and Miyamoto H. Shematrin: a family of glycine-rich structural proteins in the shell of the pearl oyster Pinctada fucata. Comp. Biochem. Physiol. B 144 (2006) 254-262