全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Daphnia as an Emerging Epigenetic Model Organism

DOI: 10.1155/2012/147892

Full-Text   Cite this paper   Add to My Lib

Abstract:

Daphnia offer a variety of benefits for the study of epigenetics. Daphnia’s parthenogenetic life cycle allows the study of epigenetic effects in the absence of confounding genetic differences. Sex determination and sexual reproduction are epigenetically determined as are several other well-studied alternate phenotypes that arise in response to environmental stressors. Additionally, there is a large body of ecological literature available, recently complemented by the genome sequence of one species and transgenic technology. DNA methylation has been shown to be altered in response to toxicants and heavy metals, although investigation of other epigenetic mechanisms is only beginning. More thorough studies on DNA methylation as well as investigation of histone modifications and RNAi in sex determination and predator-induced defenses using this ecologically and evolutionarily important organism will contribute to our understanding of epigenetics. 1. Introduction The unusual life cycle of the freshwater microcrustacean, Daphnia, has been studied for more than 150 years [1]. Most species are cyclic parthenogens able to produce two types of eggs, diploid parthenogenetic eggs or haploid sexual eggs, in response to environmental cues [2, 3]. Sex determination is likewise environmentally controlled; males are produced in response to suitable environmental cues [3]. Additionally, Daphnia exhibit a range of spectacular polyphenisms, phenotypic alternations including helmet and neckteeth formation, in response to predators [4, 5]. This makes Daphnia an excellent candidate for studying environmental influences on epigenetic developmental programs. Most importantly in the context of epigenetics, clonal lines are genetically identical yet consist of phenotypically divergent individuals. This offers a unique opportunity to separate genetic and epigenetic influences on the phenotype, an invaluable asset when studying epigenetics. The attractiveness of Daphnia as a potential epigenetic model organism is further enhanced by the fact that they are easy and inexpensive to maintain and have a rapid life cycle. As a primary consumer and a food source for invertebrates and fish [6], there is an extensive body of literature on their ecological role, development, and the evolution of parthenogenesis. Thus, Daphnia is an ecologically important organism well-studied in the context of evolution, ecology, ecotoxicology, predator-induced polyphenisms, and genomics [7, 8] and offers unparalleled opportunities to study epigenetics in these biologically important processes. Epigenetics

References

[1]  J. Lubbock, “An account of the two methods of reproduction in Daphnia, and of the structure of ephippium,” Philosophical Transactions of the Royal Society, vol. 57, pp. 79–100, 1857.
[2]  F. Zaffagnini, “Reproduction in Daphnia,” in Daphnia, R. H. Peters and R. De Bernardi, Eds., vol. 45 of Memorie dellIstituto Italiano di Idrobiologia, pp. 245–284, 1987.
[3]  O. T. Kleiven, P. Larsson, and A. Hobaek, “Sexual reproduction in Daphnia magna requires three stimuli,” Oikos, vol. 65, no. 2, pp. 197–206, 1992.
[4]  M. B. Vandegehuchte and C.R. Janssen, “Epigenetics and its implications for ecotoxicology,” Ecotoxicology, vol. 20, pp. 607–624, 2011.
[5]  L. J. Weider and J. Pijanowska, “Plasticity of Daphnia life histories in response to chemical cues from predators,” Oikos, vol. 67, no. 3, pp. 385–392, 1993.
[6]  J. K. Colbourne, P. D. N. Hebert, and D. J. Taylor, “Evolutionary origins of phenotypic diversity in Daphnia,” in Molecular Evolution and Adaptive Radiation, T. J. Givnish and K. J. Sytsma, Eds., pp. 163–188, Cambridge University Press, Cambridge, UK, 1997.
[7]  A. Stollewerk, “The water flea Daphnia—a “new” model system for ecology and evolution?” Journal of Biology, vol. 9, no. 2, article 21, 2010.
[8]  D. Ebert, Ecology, Epidemiology, and Evolution of Parasitism in Daphnia, National Library of Medicine (US), National Center for Biotechnology Information, Bethesda, Md, USA, 2005, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Books/.
[9]  R. Jaenisch and A. Bird, “Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals,” Nature Genetics, vol. 33, pp. 245–254, 2003.
[10]  K. F. Santos, T. N. Mazzola, and H. F. Carvalho, “The prima donna of epigenetics: the regulation of gene expression by DNA methylation,” Brazilian Journal of Medical and Biological Research, vol. 38, no. 10, pp. 1531–1541, 2005.
[11]  F. Fuks, “DNA methylation and histone modifications: teaming up to silence genes,” Current Opinion in Genetics and Development, vol. 15, no. 5, pp. 490–495, 2005.
[12]  A. Lennartsson and K. Ekwall, “Histone modification patterns and epigenetic codes,” Biochimica et Biophysica Acta, vol. 1790, no. 9, pp. 863–868, 2009.
[13]  Z. Lippman and R. Martienssen, “The role of RNA interference in heterochromatic silencing,” Nature, vol. 431, no. 7006, pp. 364–370, 2004.
[14]  R. W. Carthew and E. J. Sontheimer, “Origins and Mechanisms of miRNAs and siRNAs,” Cell, vol. 136, no. 4, pp. 642–655, 2009.
[15]  S. M. Reamon-Buettner, V. Mutschler, and J. Borlak, “The next innovation cycle in toxicogenomics: environmental epigenetics,” Mutation Research, vol. 659, no. 1-2, pp. 158–165, 2008.
[16]  A. A. Agrawal, C. Laforsch, and R. Tollrian, “Transgenerational induction of defences in animals and plants,” Nature, vol. 401, no. 6748, pp. 60–63, 1999.
[17]  F. Johannes, E. Porcher, F. K. Teixeira et al., “Assessing the impact of transgenerational epigenetic variation on complex traits,” PLoS Genetics, vol. 5, no. 6, Article ID e1000530, 2009.
[18]  J. E. Cropley, C. M. Suter, K. B. Beckman, and D. I. K. Martin, “Germ-line epigenetic modification of the murine Avy allele by nutritional supplementation,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 46, pp. 17308–17312, 2006.
[19]  Y. Xing, S. Shi, L. Le, C. A. Lee, L. Silver-Morse, and W. X. Li, “Evidence for transgenerational transmission of epigenetic tumor susceptibility in Drosophila,” PLoS Genetics, vol. 3, no. 9, pp. 1598–1606, 2007.
[20]  N. A. Youngson and E. Whitelaw, “Transgenerational epigenetic effects,” Annual Review of Genomics and Human Genetics, vol. 9, pp. 233–257, 2008.
[21]  D. K. Morgan and E. Whitelaw, “The case for transgenerational epigenetic inheritance in humans,” Mammalian Genome, vol. 19, no. 6, pp. 394–397, 2008.
[22]  Y. Ojima, “A cytological study on the development and maturation of the parthenogenetic and sezual eggs of Daphnia pulex (Crustacea-Cladocera),” Kwansei Gakuin Unic Ann Studies, vol. 6, pp. 123–176, 1958.
[23]  D. Tsuchiya, B. D. Eads, and M. E. Zolan, “Methods for meiotic chromosome preparation, immunofluorescence, and fluorescence in situ hybridization in Daphnia pulex,” Methods in Molecular Biology, vol. 558, pp. 235–249, 2009.
[24]  T. Cremer and C. Cremer, “Chromosome territories, nuclear architecture and gene regulation in mammalian cells,” Nature Reviews Genetics, vol. 2, no. 4, pp. 292–301, 2001.
[25]  J. K. Colbourne, M. E. Pfrender, D. Gilbert et al., “The ecoresponsive genome of Daphnia pulex,” Science, vol. 331, no. 6017, pp. 555–561, 2011.
[26]  A. Soetaert, K. van der Ven, L. N. Moens, T. Vandenbrouck, P. van Remortel, and W. M. De Coen, “Daphnia magna and ecotoxicogenomics: gene expression profiles of the anti-ecdysteroidal fungicide fenarimol using energy-, molting- and life stage-related cDNA libraries,” Chemosphere, vol. 67, no. 1, pp. 60–71, 2007.
[27]  V. Obreshkove and A.W. Fraser, “Growth and differentiation of Daphnia magna eggs in vitro,” Biological Bulletin, vol. 78, pp. 428–436, 1940.
[28]  C. Laforsch and R. Tollrian, “Embryological aspects of inducible morphological defenses in Daphnia,” Journal of Morphology, vol. 262, no. 3, pp. 701–707, 2004.
[29]  K. Sagawa, H. Yamagata, and Y. Shiga, “Exploring embryonic germ line development in the water flea, Daphnia magna, by zinc-finger-containing VASA as a marker,” Gene Expression Patterns, vol. 5, no. 5, pp. 669–678, 2005.
[30]  C. D. Robinson, S. Lourido, S. P. Whelan, J. L. Dudycha, M. Lynch, and S. Isern, “Viral transgenesis of embryonic cell cultures from the freshwater microcrustacean Daphnia,” Journal of Experimental Zoology, vol. 305, no. 1, pp. 62–67, 2006.
[31]  Y. Kato, K. Kobayashi, H. Watanabe, and T. Iguchi, “Introduction of foreign DNA into the water flea, Daphnia magna, by electroporation,” Ecotoxicology, vol. 19, no. 3, pp. 589–592, 2010.
[32]  Y. Kato, Y. Shiga, K. Kobayashi et al., “Development of an RNA interference method in the cladoceran crustacean Daphnia magna,” Development Genes and Evolution, vol. 220, no. 11-12, pp. 337–345, 2011.
[33]  Y. Kato, K. Kobayashi, H. Watanabe, and T. Iguchi, “Environmental sex determination in the branchiopod crustacean Daphnia magna: deep conservation of a Doublesex gene in the sex-determining pathway,” PLoS Genetics, vol. 7, no. 3, Article ID e1001345, 2011.
[34]  M. B. Vandegehuchte, F. Lemière, L. Vanhaecke, W. Vanden Berghe, and C. R. Janssen, “Direct and transgenerational impact on Daphnia magna of chemicals with a known effect on DNA methylation,” Comparative Biochemistry and Physiology, vol. 151, no. 3, pp. 278–285, 2010.
[35]  M. B. Vandegehuchte, D. De Coninck, T. Vandenbrouck, W. M. De Coen, and C. R. Janssen, “Gene transcription profiles, global DNA methylation and potential transgenerational epigenetic effects related to Zn exposure history in Daphnia magna,” Environmental Pollution, vol. 158, no. 10, pp. 3323–3329, 2010.
[36]  M. B. Vandegehuchte, T. Vandenbrouck, D. D. Coninck, W. M. De Coen, and C. R. Janssen, “Can metal stress induce transferable changes in gene transcription in Daphnia magna?” Aquatic Toxicology, vol. 97, no. 3, pp. 188–195, 2010.
[37]  M. B. Vandegehuchte, F. Lemière, and C. R. Janssen, “Quantitative DNA-methylation in Daphnia magna and effects of multigeneration Zn exposure,” Comparative Biochemistry and Physiology, vol. 150, no. 3, pp. 343–348, 2009.
[38]  S. T. Threlkeld, “Daphnia life history strategies and resource allocation patterns,” in Daphnia, R. H. Peters and R. De Bernardi, Eds., vol. 45 of Memorie dellIstituto Italiano di Idrobiologia, pp. 353–366, 1987.
[39]  A. M. Schurko, J. M. Logsdon, and B. D. Eads, “Meiosis genes in Daphnia pulex and the role of parthenogenesis in genome evolution,” BMC Evolutionary Biology, vol. 9, no. 1, article 78, 2009.
[40]  C. Hiruta, C. Nishida, and S. Tochinai, “Abortive meiosis in the oogenesis of parthenogenetic Daphnia pulex,” Chromosome Research, vol. 18, no. 7, pp. 833–849, 2010.
[41]  P. D. Hebert and R. D. Ward, “Inheritance during parthenogenesis in Daphnia magna,” Genetics, vol. 71, no. 4, pp. 639–642, 1972.
[42]  A. R. Omilian, M. E. A. Cristescu, J. L. Dudycha, and M. Lynch, “Ameiotic recombination in asexual lineages of Daphnia,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 49, pp. 18638–18643, 2006.
[43]  F. Zaffagnini and B. Sabelli, “Karyologic observations on the maturation of the summer and winter Eggs of Daphnia pulex and Daphnia middendorffiana,” Chromosoma, vol. 36, no. 2, pp. 193–203, 1972.
[44]  K. K. Sanford, “The effect of temperature on the intersex character of Daphnia longispina,” Physiological Zoology, vol. 20, pp. 325–332, 1947.
[45]  A. W. Olmstead and G. A. LeBlanc, “The environmental-endocrine basis of gynandromorphism (intersex) in a crustacean,” International Journal of Biological Sciences, vol. 3, no. 2, pp. 77–84, 2007.
[46]  S. S. Schwartz and P. D. N. Hebert, “Daphniopsis ephemeralis sp.n. ( Cladocera, Daphniidae): a new genus for North America,” The Canadian Journal of Zoology, vol. 63, no. 11, pp. 2689–2693, 1985.
[47]  B. D. Eads, J. K. Colbourne, E. Bohuski, and J. Andrews, “Profiling sex-biased gene expression during parthenogenetic reproduction in Daphnia pulex,” BMC Genomics, vol. 8, article 464, 2007.
[48]  R. Tollrian and S. T. Dodson, “Inducible defenses in Cladocera: constraints, costs, and multipredator environments,” in The Ecology and Evolution of Inducible Defenses, R. Tollrian and C. D. Harvell, Eds., pp. 177–202, Princeton University Press, Princeton, NJ, USA, 1999.
[49]  R. Tollrian, “Predator-induced helmet formation in Daphnia cucullata (Sars),” Archiv fur Hydrobiologie, vol. 119, pp. 191–196, 1990.
[50]  M. J. Beaton and P. D. N. Hebert, “Patterns of DNA synthesis and mitotic activity during the intermoult of Daphnia,” Journal of Experimental Zoology, vol. 268, no. 5, pp. 400–409, 1994.
[51]  H. Miyakawa, M. Imai, N. Sugimoto et al., “Gene up-regulation in response to predator kairomones in the water flea, Daphnia pulex,” BMC Developmental Biology, vol. 10, article 45, 2010.
[52]  M. Imai, Y. Naraki, S. Tochinai, and T. Miura, “Elaborate regulations of the predator-induced polyphenism in the water flea Daphnia pulex: Kairomone-sensitive periods and life-history tradeoffs,” Journal of Experimental Zoology, vol. 311, no. 10, pp. 788–795, 2009.
[53]  D. Lemons and W. McGinnis, “Genomic evolution of hox gene clusters,” Science, vol. 313, no. 5795, pp. 1918–1922, 2006.
[54]  C. Rauskolb, M. Peifer, and E. Wieschaus, “extradenticle, a regulator of homeotic gene activity, is a homolog of the homeobox-containing human proto-oncogene pbx1,” Cell, vol. 74, no. 6, pp. 1101–1112, 1993.
[55]  K. Miura, M. Oda, S. Makita, and Y. Chinzei, “Characterization of the Drosophila Methoprene-tolerant gene product: Juvenile hormone binding and ligand-dependent gene regulation,” FEBS Journal, vol. 272, no. 5, pp. 1169–1178, 2005.
[56]  M. B. Vandegehuchte, T. Vandenbrouck, D. De Coninck, W. M. De Coen, and C. R. Janssen, “Gene transcription and higher-level effects of multigenerational Zn exposure in Daphnia magna,” Chemosphere, vol. 80, no. 9, pp. 1014–1020, 2010.
[57]  M. B. Vandegehuchte, T. Kyndt, B. Vanholme, A. Haegeman, G. Gheysen, and C. R. Janssen, “Occurrence of DNA methylation in Daphnia magna and influence of multigeneration Cd exposure,” Environment International, vol. 35, no. 4, pp. 700–706, 2009.
[58]  A. Baccarelli and V. Bollati, “Epigenetics and environmental chemicals,” Current Opinion in Pediatrics, vol. 21, no. 2, pp. 243–251, 2009.
[59]  D. C. Dolinoy, D. Huang, and R. L. Jirtle, “Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 32, pp. 13056–13061, 2007.
[60]  S. Feng, S. E. Jacobsen, and W. Reik, “Epigenetic reprogramming in plant and animal development,” Science, vol. 330, no. 6004, pp. 622–627, 2010.
[61]  M. Z. Fang, D. Chen, Y. Sun, Z. Jin, J. K. Christman, and C. S. Yang, “Reversal of hypermethylation and reactivation of p16INK4a, RARβ, and MGMT genes by genistein and other isoflavones from soy,” Clinical Cancer Research, vol. 11, no. 19 I, pp. 7033–7041, 2005.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133