Studies on the pinctada fucata BMP-2 Gene: Structural similarity and functional conservation of its osteogenic potential within the animal kingdom

International Journal of Zoology

Volumn 2013, Issue , 2013, Pages

  Takami, Akiko ^a   Kato, Hirotaka ^a   Takagi, Ryousuke ^a   Miyashita, Tomoyuki ^a  

^a KINKI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84877265124     PISSN: 16878477     EISSN: 16878485     Source Type: Journal    
DOI: 10.1155/2013/787323     Document Type: Article

References (42)

1. Derynck R., Miyazono K., Derynck R., Miyazono K., TGF-beta and the TGF-beta family. The TGF-Beta Family 2008 New York, NY, USA Cold Spring Harbor Laboratory Press 29 43
2. Derynck R., Akhurst R. J., Differentiation plasticity regulated by TGF- β family proteins in development and disease. Nature Cell Biology 2007 9 9 1000 1004 2-s2.0-34548329486 10.1038/ncb434 (Pubitemid 47338137)
3. Li Q., Agno J. E., Edson M. A., Nagaraja A. K., Nagashima T., Matzuk M. M., Transforming growth factor β receptor type 1 is essential for female reproductive tract integrity and function. PLoS Genetics 2011 7 e1002320
4. Nederbragt A. J., van Loon A. E., Dictus W. J. A. G., Expression of Patella vulgata orthologs of engrailed and dpp-BMP2/4 in adjacent domains during molluscan shell development suggests a conserved compartment boundary mechanism. Developmental Biology 2002 246 2 341 355 2-s2.0-0036067868 10.1006/dbio.2002.0653 (Pubitemid 34775351)
5. Iijima M., Takeuchi T., Sarashina I., Endo K., Expression patterns of engrailed and dpp in the gastropod Lymnaea stagnalis. Development Genes and Evolution 2008 218 5 237 251 2-s2.0-43049087352 10.1007/s00427-008-0217-0
6. Lelong C., Mathieu M., Favrel P., Structure and expression of mGDF, a new member of the transforming growth factor- β supwrfamily in the bivalve mollusc Crassostrea gigas. European Journal of Biochemistry 2000 267 13 3986 3993 2-s2.0-0033921029 10.1046/j.1432-1327.2000.01432.x (Pubitemid 30436089)
7. Herpin A., Lelong C., Becker T., Rosa F., Favrel P., Cunningham C., Structural and functional evidence for a singular repertoire of BMP receptor signal transducing proteins in the lophotrochozoan Crassostrea gigas suggests a shared ancestral BMP/activin pathway. FEBS Journal 2005 272 13 3424 3440 2-s2.0-22144459078 10.1111/j.1742-4658.2005.04761.x (Pubitemid 40979312)
8. Miyashita T., Hanashita T., Toriyama M., Takagi R., Akashika T., Higashikubo N., Gene cloning and biochemical characterization of the BMP-2 of Pinctada fucata. Bioscience, Biotechnology and Biochemistry 2008 72 1 37 47 2-s2.0-38549159892 10.1271/bbb.70302 (Pubitemid 351158950)
9. Li C., Hu Y., Liang J., Kong Y., Huang J., Feng Q., Li S., Zhang G., Xie L., Zhang R., Calcineurin plays an important role in the shell formation of pearl oyster (Pinctada fucata). Marine Biotechnology 2010 12 1 100 110 2-s2.0-76349085419 10.1007/s10126-009-9204-3
10. Helvering L. M., Sharp R. L., Ou X., Geiser A. G., Regulation of the promoters for the human bone morphogenetic protein 2 and 4 genes. Gene 2000 256 1-2 123 138 2-s2.0-0034601692 10.1016/S0378-1119(00)00364-4
11. Tomita M., Reinhold M. I., Molkentin J. D., Naski M. C., Calcineurin and NFAT4 induce chondrogenesis. Journal of Biological Chemistry 2002 277 44 42214 42218 2-s2.0-0036828714 10.1074/jbc.C200504200 (Pubitemid 35257540)
12. Lopez E., Vidal B., Berland S., Camprasse S., Camprasse G., Silve C., Demonstration of the capacity of nacre to induce bone formation by human osteoblasts maintained in vitro. Tissue and Cell 1992 24 5 667 679 2-s2.0-0026453503 10.1016/0040-8166(92)90037-8
13. Silve C., Lopez E., Vidal B., Smith D. C., Camprasse S., Camprasse G., Couly G., Nacre initiates biomineralization by human osteoblasts maintained in vitro. Calcified Tissue International 1992 51 5 363 369 2-s2.0-0027096774 10.1007/BF00316881 (Pubitemid 23019416)
14. Lamghari M., Almeida M. J., Berland S., Huet H., Laurent A., Milet C., Lopez E., Stimulation of bone marrow cells and bone formation by nacre: in vivo and in vitro studies. Bone 1999 25 1 91S 94S 2-s2.0-0032803046 10.1016/S8756-3282(99)00141-6 (Pubitemid 29333188)
15. Liao H., Mutvei H., Hammarström L., Wurtz T., Li J., Tissue responses to nacreous implants in rat femur: an in situ hybridization and histochemical study. Biomaterials 2002 23 13 2693 2701 2-s2.0-0036249891 10.1016/S0142-9612(01)00421-5 (Pubitemid 34467048)
16. Westbroek P., Marin F., A marriage of bone and nacre. Nature 1998 392 6679 861 862 2-s2.0-0032580154 10.1038/31798 (Pubitemid 28232039)
17. Sampath T. K., Rashka K. E., Doctor J. S., Tucker R. F., Hoffmann F. M., Drosophila transforming growth factor β superfamily proteins induce endochondral bone formation in mammals. Proceedings of the National Academy of Sciences of the United States of America 1993 90 13 6004 6008 2-s2.0-0027161383 (Pubitemid 23191442)
18. Pagni M., Junier T., Dotlet: powerful and easy strategy for pairwise comparisons. Journal of Cell and Molecular Biology 2010 7-8 1-2 81 82
19. Miyashita T., Hirotaka K., Takagi R., Expression and purification of the recombinant mature bone morphogenetic protein-2 of Pinctada fucata in Escherichia coli and comparison of the codon usage. Memoirs of the School of Biology-Oriented Science and Technology of Kinki University 2006 18 1 7
20. Reznikoff C. A., Brankow D. W., Heidelberger C., Establishment and characterization of a cloned line of C3H mouse embryo cells sensitive to postconfluence inhibition of division. Cancer Research 1973 33 12 3231 3238 2-s2.0-0015752438
21. Suzuki Y., Tanihara M., Suzuki K., Saitou A., Nishimura Y., Alginate hydrogel linked with synthetic oligopeptide derived from BMP-2 allows ectopic osteoinduction in vivo. Journal of Biomedical Materials Research 2000 50 405 409 (Pubitemid 30180733)
22. Saito A., Suzuki Y., Ogata S. I., Ohtsuki C., Tanihara M., Activation of osteo-progenitor cells by a novel synthetic peptide derived from the bone morphogenetic protein-2 knuckle epitope. Biochimica et Biophysica Acta 2003 1651 1-2 60 67 2-s2.0-0642341968 10.1016/S1570-9639(03)00235-8 (Pubitemid 38234553)
23. Franceschi R. T., The developmental control of osteoblast-specific gene expression: role of specific transcription factors and the extracellular matrix environment. Critical Reviews in Oral Biology and Medicine 1999 10 1 40 57 2-s2.0-0032737614 (Pubitemid 29510046)
24. Frith J., Genever P., Transcriptional control of mesenchymal stem cell differentiation. Transfusion Medicine and Hemotherapy 2008 35 3 216 227 2-s2.0-49649083563 10.1159/000127448
25. Nishimura R., Hata K., Matsubara T., Wakabayashi M., Yoneda T., Regulation of bone and cartilage development by network between BMP signalling and transcription factors. The Journal of Biochemistry 2012 151 247 254 10.1093/jb/mvs004
26. Chen G., Deng C., Li Y. P., TGF- β and BMP signaling in osteoblast differentiation and bone formation. International Journal of Biological Sciences 2012 8 2 272 288 10.7150/ijbs.2929
27. Ulsamer A., Ortuño M. J., Ruiz S., Susperregui A. R. G., Osses N., Rosa J. L., Ventura F., BMP-2 induces Osterix expression through up-regulation of Dlx5 and its phosphorylation by p38. Journal of Biological Chemistry 2008 283 7 3816 3826
28. Lee M. H., Kim Y. J., Yoon W. J., Kim J. I., Kim B. G., Hwang Y. S., Wozney J. M., Chi X. Z., Bae S. C., Choi K. Y., Cho J. Y., Choi J. Y., Ryoo H. M., Dlx5 specifically regulates Runx2 type II expression by binding to homeodomain-response elements in the Runx2 distal promoter. Journal of Biological Chemistry 2005 280 42 35579 35587 2-s2.0-27444447372 10.1074/jbc.M502267200 (Pubitemid 41532750)
29. Komori T., Regulation of osteoblast differentiation by Runx2. Advances in Experimental Medicine and Biology 2010 658 43 49 2-s2.0-77953686495 10.1007/978-1-4419-1050-9-5
30. Miyamoto H., Miyashita T., Okushima M., Nakano S., Morita T., Matsushiro A., A carbonic anhydrase from the nacreous layer in oyster pearls. Proceedings of the National Academy of Sciences of the United States of America 1996 93 18 9657 9660 2-s2.0-0029821928
31. Samata T., Hayashi N., Kono M., Hasegawa K., Horita C., Akera S., A new matrix protein family related to the nacreous layer formation of Pinctada fucata. FEBS Letters 1999 462 1-2 225 229 2-s2.0-0032712041 10.1016/S0014- 5793(99)01387-3
32. Miyashita T., Takagi R., Okushima M., Nakano S., Miyamoto H., Nishikawa E., Matsushiro A., Complementary DNA cloning and characterization of Pearlin, a new class of matrix protein in the nacreous layer of oyster pearls. Marine Biotechnology 2000 2 5 409 418 2-s2.0-0033666992
33. Yano M., Nagai K., Morimoto K., Miyamoto H., A novel nacre protein N19 in the pearl oyster Pinctada fucata. Biochemical and Biophysical Research Communications 2007 362 158 163 (Pubitemid 47296306)
34. Suzuki M., Saruwatari K., Kogure T., Yamamoto Y., Nishimura T., Kato T., Nagasawa H., An acidic matrix protein, Pif, is a key macromolecule for nacre formation. Science 2009 325 5946 1388 1390 2-s2.0-70249111462 10.1126/science.1173793
35. Suzuki M., Murayama E., Inoue H., Ozaki N., Tohse H., Kogure T., Nagasawa H., Characterization of Prismalin-14, a novel matrix protein from the prismatic layer of the Japanese pearl oyster (Pinctada fucata). Biochemical Journal 2004 382 1 205 213 2-s2.0-4344712499 10.1042/BJ20040319 (Pubitemid 39141583)
36. Miyashita T., Takami A., Takagi R., Molecular cloning and characterization of the 5′-flanking regulatory region of the carbonic anhydrase nacrein gene of the pearl oyster Pinctada fucata and its expression. Biochemical Genetics 2012 50 9-10 673 683 10.1007/s10528-012-9510-8
37. Wang E. A., Rosen V., D'Alessandro J. S., Bauduy M., Cordes P., Harada T., Israel D. I., Hewick R. M., Kerns K. M., LaPan P., Luxenberg D. P., McQuaid D., Moutsatsos I. K., Nove J., Wozney J. M., Recombinant human bone morphogenetic protein induces bone formation. Proceedings of the National Academy of Sciences of the United States of America 1990 87 6 2220 2224 2-s2.0-0025216220
38. Rider C. C., Mulloy B., Bone morphogenetic protein and growth differentiation factor cytokine families and their protein antagonists. Biochemical Journal 2010 429 1 1 12 2-s2.0-77954527232 10.1042/BJ20100305
39. Ozkaynak E., Schnegelsberg P. N. J., Jin D. F., Clifford G. M., Warren F. D., Drier E. A., Oppermann H., Osteogenic protein-2. A new member of the transforming growth factor- β superfamily expressed early in embryogenesis. Journal of Biological Chemistry 1992 267 35 25220 25227 2-s2.0-0026459795
40. Groppe J., Rumpel K., Economides A. N., Stahl N., Sebald W., Affolter M., Biochemical and biophysical characterization of refolded Drosophila DPP, a homolog of bone morphogenetic proteins 2 and 4. Journal of Biological Chemistry 1998 273 44 29052 29065 2-s2.0-0032582505 10.1074/jbc.273.44.29052 (Pubitemid 28507601)
41. Zhou J.-J. A., Enhancing production of recombinant BMP-2 in mammalian cell culture systems by inhibition of pro-protein cleavage using 9DR peptides [M.S. thesis] 2008 University of Toronto
42. Saremba S., Nickel J., Seher A., Kotzsch A., Sebald W., Mueller T. D., Type I receptor binding of bone morphogenetic protein 6 is dependent on N-glycosylation of the ligand. FEBS Journal 2008 275 1 172 183 2-s2.0-37349118993 10.1111/j.1742-4658.2007.06187.x (Pubitemid 350294073)