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DNA Methylation, Epigenetics, and Evolution in Vertebrates: Facts and Challenges

DOI: 10.1155/2014/475981

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Abstract:

DNA methylation is a key epigenetic modification in the vertebrate genomes known to be involved in biological processes such as regulation of gene expression, DNA structure and control of transposable elements. Despite increasing knowledge about DNA methylation, we still lack a complete understanding of its specific functions and correlation with environment and gene expression in diverse organisms. To understand how global DNA methylation levels changed under environmental influence during vertebrate evolution, we analyzed its distribution pattern along the whole genome in mammals, reptiles and fishes showing that it is correlated with temperature, independently on phylogenetic inheritance. Other studies in mammals and plants have evidenced that environmental stimuli can promote epigenetic changes that, in turn, might generate localized changes in DNA sequence resulting in phenotypic effects. All these observations suggest that environment can affect the epigenome of vertebrates by generating hugely different methylation patterns that could, possibly, reflect in phenotypic differences. We are at the first steps towards the understanding of mechanisms that underlie the role of environment in molding the entire genome over evolutionary times. The next challenge will be to map similarities and differences of DNA methylation in vertebrates and to associate them with environmental adaptation and evolution. 1. Environmental Epigenetics and DNA Methylation In vertebrates, cytosine DNA methylation is a heritable epigenetic modification that occurs mostly at the CpG dinucleotides except for the CpGs in CpG islands [1]. Recently, it has become extremely attractive given its involvement in a diverse range of cellular functions including tissue-specific gene expression, cell differentiation [2], development [3, 4] and reprogramming ([5] see references therein), genomic imprinting, X chromosome inactivation, and regulation of chromatin structure and disease states [6–9]. Notably, the epigenome contains hypervariable regions that could be a source of cellular diversity [10] or could underlie disease states or provide an engine for neutral selection at cell or tissue level [11]. Such hypervariability might be influenced by metabolite fluctuations, temperature variation, and other environmental agents that exert their action on chromatin-modifying enzymes and gene regulation [12–15]. A clear example of how environment plays an important role in shaping the epigenome is represented by monozygotic twins, who are epigenetically indistinguishable early in life but with

References

[1]  M. Weber, J. J. Davies, D. Wittig et al., “Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells,” Nature Genetics, vol. 37, no. 8, pp. 853–862, 2005.
[2]  L. Jackson-Grusby, C. Beard, R. Possemato et al., “Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation,” Nature Genetics, vol. 27, no. 1, pp. 31–39, 2001.
[3]  M. Okano, D. W. Bell, D. A. Haber, and E. Li, “DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development,” Cell, vol. 99, no. 3, pp. 247–257, 1999.
[4]  W. Reik, W. Dean, and J. Walter, “Epigenetic reprogramming in mammalian development,” Science, vol. 293, no. 5532, pp. 1089–1093, 2001.
[5]  K. B. Dobbs, M. Rodriguez, M. J. Sudano, M. S. Ortega, and P. J. Hansen, “Dynamics of DNA methylation during early development of the preimplantation bovine embryo,” PLoS ONE, vol. 8, no. 6, Article ID e66230, 2013.
[6]  A. Bird, “DNA methylation patterns and epigenetic memory,” Genes and Development, vol. 16, no. 1, pp. 6–21, 2002.
[7]  A. E. Peaston and E. Whitelaw, “Epigenetics and phenotypic variation in mammals,” Mammalian Genome, vol. 17, no. 5, pp. 365–374, 2006.
[8]  V. Bollati and A. Baccarelli, “Environmental epigenetics,” Heredity, vol. 105, no. 1, pp. 105–112, 2010.
[9]  C. Faulk and D. C. Dolinoy, “Timing is everything: the when and how of environmentally induced changes in the epigenome of animals,” Epigenetics, vol. 6, no. 7, pp. 791–797, 2011.
[10]  M. M. Suzuki and A. Bird, “DNA methylation landscapes: provocative insights from epigenomics,” Nature Reviews Genetics, vol. 9, no. 6, pp. 465–476, 2008.
[11]  J.-P. Issa, “Epigenetic variation and cellular Darwinism,” Nature Genetics, vol. 43, no. 8, pp. 724–726, 2011.
[12]  R. A. Waterland and R. L. Jirtle, “Early nutrition, epigenetic changes at transposons and imprinted genes, and enhanced susceptibility to adult chronic diseases,” Nutrition, vol. 20, no. 1, pp. 63–68, 2004.
[13]  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.
[14]  N. Gilbert, I. Thomson, S. Boyle, J. Allan, B. Ramsahoye, and W. A. Bickmore, “DNA methylation affects nuclear organization, histone modifications, and linker histone binding but not chromatin compaction,” Journal of Cell Biology, vol. 177, no. 3, pp. 401–411, 2007.
[15]  V. Chinnusamy and J.-K. Zhu, “Epigenetic regulation of stress responses in plants,” Current Opinion in Plant Biology, vol. 12, no. 2, pp. 133–139, 2009.
[16]  M. F. Fraga, E. Ballestar, M. F. Paz et al., “Epigenetic differences arise during the lifetime of monozygotic twins,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 30, pp. 10604–10609, 2005.
[17]  E. J. Finnegan and E. S. Dennis, “Vernalization-induced trimethylation of histone H3 lysine 27 at FLC is not maintained in mitotically quiescent cells,” Current Biology, vol. 17, no. 22, pp. 1978–1983, 2007.
[18]  R. J. Schmitz, S. Sung, and R. M. Amasino, “Histone arginine methylation is required for vernalization-induced epigenetic silencing of FLC in winter-annual Arabidopsis thaliana,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 2, pp. 411–416, 2008.
[19]  M. D. Anway, A. S. Cupp, M. Uzumcu, and M. K. Skinner, “Toxicology: epigenetic transgenerational actions of endocrine disruptors and male fertility,” Science, vol. 308, no. 5727, pp. 1466–1469, 2005.
[20]  é. Danchin, A. Charmantier, F. A. Champagne, A. Mesoudi, B. Pujol, and S. Blanchet, “Beyond DNA: integrating inclusive inheritance into an extended theory of evolution,” Nature Reviews Genetics, vol. 12, no. 7, pp. 475–486, 2011.
[21]  A. Petronis, “Epigenetics as a unifying principle in the aetiology of complex traits and diseases,” Nature, vol. 465, no. 7299, pp. 721–727, 2010.
[22]  M. Jakovcevski and S. Akbarian, “Epigenetic mechanisms in neurological disease,” Nature Medicine, vol. 18, pp. 1194–1204, 2012.
[23]  E. Ballestar and M. Esteller, “Methyl-CpG-binding proteins in cancer: blaming the DNA methylation messenger,” Biochemistry and Cell Biology, vol. 83, no. 3, pp. 374–384, 2005.
[24]  K. D. Hansen, W. Timp, H. C. Bravo et al., “Increased methylation variation in epigenetic domains across cancer types,” Nature Genetics, vol. 43, no. 8, pp. 768–775, 2011.
[25]  K. D. Robertson, “DNA methylation and human disease,” Nature Reviews Genetics, vol. 6, no. 8, pp. 597–610, 2005.
[26]  M. Esteller and J. G. Herman, “Cancer as an epigenetic disease: DNA methylation and chromatin alterations in human tumours,” Journal of Pathology, vol. 196, no. 1, pp. 1–7, 2002.
[27]  E. Jablonka and M. J. Lamb, “Précis of evolution in four dimensions,” Journal of Behavioral and Brain Science, vol. 30, pp. 353–365, 2007.
[28]  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.
[29]  R. Rebollo, B. Horard, B. Hubert, and C. Vieira, “Jumping genes and epigenetics: towards new species,” Gene, vol. 454, no. 1-2, pp. 1–7, 2010.
[30]  O. Bossdorf, C. L. Richards, and M. Pigliucci, “Epigenetics for ecologists,” Ecology Letters, vol. 11, no. 2, pp. 106–115, 2008.
[31]  F. Johannes, V. Colot, and R. C. Jansen, “Epigenome dynamics: a quantitative genetics perspective,” Nature Reviews Genetics, vol. 9, no. 11, pp. 883–890, 2008.
[32]  C. L. Richards, O. Bossdorf, and K. J. F. Verhoeven, “Understanding natural epigenetic variation,” New Phytologist, vol. 187, no. 3, pp. 562–564, 2010.
[33]  L. M. Field, F. Lyko, M. Mandrioli, and G. Prantera, “DNA methylation in insects,” Insect Molecular Biology, vol. 13, no. 2, pp. 109–115, 2004.
[34]  R. J. Klose and A. P. Bird, “Genomic DNA methylation: the mark and its mediators,” Trends in Biochemical Sciences, vol. 31, no. 2, pp. 89–97, 2006.
[35]  A. Varriale and G. Bernardi, “DNA methylation and body temperature in fishes,” Gene, vol. 385, pp. 111–121, 2006.
[36]  A. Varriale and G. Bernardi, “DNA methylation in reptiles,” Gene, vol. 385, pp. 122–127, 2006.
[37]  S. Feng, S. J. Cokus, X. Zhang et al., “Conservation and divergence of methylation patterning in plants and animals,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 19, pp. 8689–8694, 2010.
[38]  A. Zemach, I. E. McDaniel, P. Silva, and D. Zilberman, “Genome-wide evolutionary analysis of eukaryotic DNA methylation,” Science, vol. 328, no. 5980, pp. 916–919, 2010.
[39]  S. B. Roberts and M. R. Gavery, “Is there a relationship between DNA methylation and phenotypic plasticity in invertebrates?” Frontiers in Physiology, vol. 2, article 116, 2012.
[40]  S. Tweedie, J. Charlton, V. Clark, and A. Bird, “Methylation of genomes and genes at the invertebrate-vertebrate boundary,” Molecular and Cellular Biology, vol. 17, no. 3, pp. 1469–1475, 1997.
[41]  M. Mandrioli and N. Volpi, “The genome of the lepidopteran Mamestra brassicae has a vertebrate-like content of methyl-cytosine,” Genetica, vol. 119, no. 2, pp. 187–191, 2003.
[42]  M. R. Kronforst, D. C. Gilley, J. E. Strassmann, and D. C. Queller, “DNA methylation is widespread across social Hymenoptera,” Current Biology, vol. 18, no. 7, pp. R287–R288, 2008.
[43]  N. Elango, B. G. Hunt, M. A. D. Goodisman, and S. V. Yi, “DNA methylation is widespread and associated with differential gene expression in castes of the honeybee, Apis mellifera,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 27, pp. 11206–11211, 2009.
[44]  Q. Li, N. Li, X. Hu et al., “Genome-wide mapping of dna methylation in chicken,” PLoS ONE, vol. 6, no. 5, Article ID e19428, 2011.
[45]  S. J. Cokus, S. Feng, X. Zhang et al., “Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning,” Nature, vol. 452, no. 7184, pp. 215–219, 2008.
[46]  R. Lister, R. C. O'Malley, J. Tonti-Filippini et al., “Highly integrated single-base resolution maps of the epigenome in Arabidopsis,” Cell, vol. 133, no. 3, pp. 523–536, 2008.
[47]  D. Zilberman, M. Gehring, R. K. Tran, T. Ballinger, and S. Henikoff, “Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription,” Nature Genetics, vol. 39, no. 1, pp. 61–69, 2007.
[48]  M. Gehring, K. L. Bubb, and S. Henikoff, “Extensive demethylation of repetitive elements during seed development underlies gene imprinting,” Science, vol. 324, no. 5933, pp. 1447–1451, 2009.
[49]  K. Jabbari, S. Cacciò, J. P. Pa?s de Barros, J. Desgrès, and G. Bernardi, “Evolutionary changes in CpG and methylation levels in the genome of vertebrates,” Gene, vol. 205, no. 1-2, pp. 109–118, 1997.
[50]  A. Varriale and G. Bernardi, “Distribution of DNA methylation, CpGs, and CpG islands in human isochores,” Genomics, vol. 95, no. 1, pp. 25–28, 2010.
[51]  T. Tatarinova, E. Elhaik, and M. Pellegrini, “Cross-species analysis of genic GC3 content and DNA methylation patterns,” Genome Biology and Evolution, vol. 5, pp. 1443–1456, 2013.
[52]  G. Bernardi, “Isochores,” in Encyclopedia of Life Sciences, John Wiley & Sons, Chichester, UK, 2012.
[53]  L. McLean, I. S. Young, M. K. Doherty et al., “Global cooling: cold acclimation and the expression of soluble proteins in carp skeletal muscle,” Proteomics, vol. 7, no. 15, pp. 2667–2681, 2007.
[54]  A. Y. Gracey, E. J. Fraser, W. Li et al., “Coping with cold: an integrative, multitissue analysis of the transcriptome of a poikilothermic vertebrate,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 48, pp. 16970–16975, 2004.
[55]  Z. Chen, C.-H. C. Cheng, J. Zhang et al., “Transcriptomic and genomic evolution under constant cold in Antarctic notothenioid fish,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 35, pp. 12944–12949, 2008.
[56]  H. S. Windisch, M. Lucassen, and S. Frickenhaus, “Evolutionary force in confamiliar marine vertebrates of different temperature realms: adaptive trends in zoarcid fish transcriptomes,” BMC Genomics, vol. 13, article 549, 2012.
[57]  D. N. Cooper and M. Krawczak, “Cytosine methylation and the fate of CpG dinucleotides in vertebrates genomes,” Human Genetics, vol. 83, no. 2, pp. 181–188, 1989.
[58]  G. Bernardi and G. Bernardi, “Compositional constraints and genome evolution,” Journal of Molecular Evolution, vol. 24, no. 1-2, pp. 1–11, 1986.
[59]  M. Pigliucci, “Modelling phenotypic plasticity. II. Do genetic correlations matter?” Heredity, vol. 77, no. 5, pp. 453–460, 1996.
[60]  C. Pál and I. Miklós, “Epigenetic inheritance, genetic assimilation and speciation,” Journal of Theoretical Biology, vol. 200, no. 1, pp. 19–37, 1999.
[61]  D. Garrick, S. Fiering, D. I. K. Martin, and E. Whitelaw, “Repeat-induced gene silencing in mammals,” Nature Genetics, vol. 18, no. 1, pp. 56–59, 1998.
[62]  E. Zuckerkandl and G. Cavalli, “Combinatorial epigenetics, “junk DNA”, and the evolution of complex organisms,” Gene, vol. 390, no. 1-2, pp. 232–242, 2007.

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