Control of shell pigmentation by secretory tubules in the abalone mantle

详细信息    查看全文

• 作者：Alyssa Budd (1)
  Carmel McDougall (1)
  Kathryn Green (2)
  Bernard M Degnan (1)
  
  1. Centre for Marine Science ; School of Biological Sciences ; The University of Queensland ; Brisbane ; QLD ; 4072 ; Australia
  2. Centre for Microscopy and Microanalysis ; The University of Queensland ; Brisbane ; QLD ; 4072 ; Australia
  
• 关键词：Mollusc ; Mantle ; Tubule ; Pigmentation ; Abalone ; Shell
• 刊名：Frontiers in Zoology
• 出版年：2014
• 出版时间：December 2014
• 年：2014
• 卷：11
• 期：1
• 全文大小：3,282 KB
• 参考文献：1. Waddington, CH, Cowe, RJ (1969) Computer simulation of a mulluscan (sic) pigmentation pattern. J Theor Biol 25: pp. 219-225 CrossRef
  2. Tabata, T, Takei, Y (2004) Morphogens, their identification and regulation. Development 131: pp. 703-712 CrossRef
  3. Lindsay, D (1982) Simulating molluscan shell pigment lines and states: implications for pattern diversity. Veliger 24: pp. 297-299
  4. Lindsay, DT (1982) A new programmatic basis for shell pigment patterns in the bivalve mollusc Lioconcha castrensis (L.). Differentiation 21: pp. 32-36 CrossRef
  5. Boettiger, A, Ermentrout, B, Oster, G (2009) The neural origins of shell structure and pattern in aquatic mollusks. Proc Natl Acad Sci U S A 106: pp. 6837-6842 CrossRef
  6. Kusch, I, Markus, M (1996) Mollusc shell pigmentation: cellular automaton simulations and evidence for undecidability. J Theor Biol 178: pp. 333-340 CrossRef
  7. Meinhardt, H (1984) Models for positional signalling, the threefold subdivision of segments and the pigmentation pattern of molluscs. J Embryol exp Morph 83: pp. 289-311
  8. Meinhardt, H, Klingler, M (1987) A model for pattern formation on the shells of molluscs. J Theor Biol 126: pp. 63-89 CrossRef
  9. Ermentrout, B, Campbell, J, Oster, G (1986) A model for shell patterns based on neural activity. Veliger 28: pp. 369-388
  10. McDougall, C, Green, K, Jackson, DJ, Degnan, BM (2011) Ultrastructure of the mantle of the gastropod Haliotis asinina and mechanisms of shell regionalization. Cells Tissues Organs 194: pp. 103-107 CrossRef
  11. Jolly, C, Berland, S, Milet, C, Borzeix, S, Lopez, E, Doumenc, D (2004) Zonal localization of shell matrix proteins in mantle of Haliotis tuberculata (Mollusca, Gastropoda). Mar Biotechnol 6: pp. 541-551 CrossRef
  12. Sud, D, Poncet, J, Saihi, A, Lebel, J, Doumenc, D, Boucaud-Camou, E (2002) A cytological study of the mantle edge of Haliotis tuberculata L. (Mollusca, Gastropoda) in relation to shell structure. J Shellfish Res 21: pp. 201-210
  13. Beedham, G (1958) Observations on the mantle of the Lamellibranchia. Quart J Mic Sci 3: pp. 181-197
  14. Lowenstam, HA, Weiner, S (1989) On Biomineralization. Oxford University Press, New York
  15. Comfort, A (1951) The pigmentation of molluscan shells. Biol Rev 26: pp. 285-301 CrossRef
  16. Needham, A (1975) The zoochromes of helicid shells. Naturwissenschaften 62: pp. 183-184 CrossRef
  17. Li, X, Bai, Z, Luo, H, Liu, Y, Wang, G, Li, J (2014) Cloning, differential tissue expression of a novel hcApo gene, and its correlation with total carotenoid content in purple and white inner-shell color pearl mussel Hyriopsis cumingii. Gene 538: pp. 258-265 CrossRef
  18. Gantsevich, M, Tyunnikova, A, Malakhov, V (2005) The genetics of shell pigmentation of the Mediterranean mussel Mytilus galloprovincialis Lamarck, 1819 (Bivalvia, Mytilida). Dokl Biol Sci 404: pp. 370-371 CrossRef
  19. Jackson, DJ, McDougall, C, Green, K, Simpson, F, W枚rheide, G, Degnan, BM (2006) A rapidly evolving secretome builds and patterns a sea shell. BMC Biol 4: pp. 40 CrossRef
  20. Jackson, DJ, McDougall, C, Woodcroft, B, Moase, P, Rose, RA, Kube, M, Reinhardt, R, Rokhsar, DS, Montagnani, C, Joubert, C, Piquemal, D, Degnan, BM (2010) Parallel evolution of nacre building gene sets in molluscs. Mol Biol Evol 27: pp. 591-608 CrossRef
  21. Marie, B, Marie, A, Jackson, DJ, Dubost, L, Degnan, BM, Milet, C, Marin, F (2010) Proteomic analysis of the organic matrix of the abalone Haliotis asinina calcified shell. Proteome Sci 8: pp. 54 CrossRef
  22. Counihan, RT, McNamara, DC, Souter, DC, Jebreen, EJ, Preston, NP, Johnson, CR, Degnan, BM (2001) Pattern, synchrony and predictability of spawning of the tropical abalone Haliotis asinina from Heron Reef, Australia. Mar Ecol Prog Ser 213: pp. 193-202 CrossRef
  23. Jackson, DJ, Ellemor, N, Degnan, BM (2005) Correlating gene expression with larval competence, and the effect of age and parentage on metamorphosis in the tropical abalone Haliotis asinina. Mar Biol 147: pp. 681-697 CrossRef
  24. Crofts, DR (1929) Haliotis. LMBC memoirs on typical British marine plants and animals 29: pp. 1-174
  25. Emberton, L (1963) Relationships between pigmentation of shell and of mantle in the snails Cepaea nemoralis (L.) and Cepaea hortensis (Mull.). Proc Zool Soc Lond 140: pp. 273-293 CrossRef
  26. Checa, AG, Salas, C, Harper, EM, Bueno-P茅rez, JD (2014) Early stage biomineralization in the periostracum of the 鈥榣iving fossil鈥?bivalve Neotrigonia. PLoS One 9: pp. e90033 CrossRef
  27. Standring, S (2008) Gray鈥檚 Anatomy: the anatomical basis of clinical practice. Elsevier, Edinburgh: Churchill Livingstone
  28. Jackson, DJ, W枚rheide, G, Degnan, BM (2007) Dynamic expression of ancient and novel molluscan shell genes during ecological transitions. BMC Evol Biol 7: pp. 160 CrossRef
  29. Jabbour-Zahab, R, Chagot, D, Blanc, F, Grizel, H (1992) Mantle histology, histochemistry and ultrastructure of the pearl oyster Pinctada margaritifera (L.). Aquat Living Resour 5: pp. 287-298 CrossRef
  30. Colville, A, Lim, R (2003) Microscopic structure of the mantle and palps in the freshwater mussels Velesunio ambiguus and Hyridella depressa (Bivalvia: Hyriidae). Molluscan Res 23: pp. 1-20 CrossRef
  31. Williams, EA, Craigie, A, Yeates, A, Degnan, SM (2008) Articulated coralline algae of the genus Amphiroa are highly effective natural inducers of settlement in the tropical abalone Haliotis asinina. Biol Bull 215: pp. 98-107 CrossRef
  32. Eisenman, E, Alfert, M (1982) A new fixation procedure for preserving the ultrastructure of marine invertebrate tissues. J Microsc 125: pp. 117-120 CrossRef
  33. Wilke, SA, Antonios, JK, Bushong, EA, Badkoobehi, A, Malek, E, Hwang, M, Terada, M, Ellisman, MH, Ghosh, A (2013) Deconstructing complexity: serial block-face electron microscopic analysis of the hippocampal mossy fiber synapse. J Neurosci 33: pp. 507-522 CrossRef
  
• 刊物主题：Zoology;
• 出版者：BioMed Central
• ISSN：1742-9994

文摘

Background Molluscan shells exhibit a wide diversity of pigmentation patterns and are often used as models for understanding the mechanisms underlying biological pattern formation. Numerous mathematical models have been put forward to describe these patterns, but all rely on assumptions regarding the nature of the pigments and the cells from which they are secreted. We investigated pigmentation and cellular morphology of the mantle (shell-secreting organ) of the tropical abalone, Haliotis asinina, as a crucial step towards understanding the molecular mechanisms of shell patterning in this gastropod mollusc. Results Accumulation and release of pigmented products occurs within secretory tubules in the prismatic zone of the juvenile H. asinina mantle. The colour observed within these tubules closely matches the colour deposited most recently within the shell lying directly above. The pigments are autofluorescent, and confocal microscopy reveals that multiple pigments can be present within a single tubule at any one time. Examination of mantle morphology in other gastropods reveals that mantle tubules are not restricted to abalone, but are not universal. Conclusions The presence of a tubule-based secretory system within the abalone mantle demonstrates that pigmentation is not controlled by a simple line of cells. Instead, co-ordination of patterning events is likely to be modular, with signals received by individual cells being transmitted throughout the entire tubule to synchronise the accumulation and secretion of pigmented material.