Epigenetics and Its Applications to Children’s Health
Abstract
Epigenetics represents the study of inheritable changes in the regulation of DNA expression during development. It represents a normal process by which totipotent early cells differentiate and commit to specific tissues, organs, and other structures that are properly arranged and are functional to enable optimum organizational performance. Exposure to nutritional deficits or excess, environmental toxins and endocrine disruptors, and both psychological and physiological stress can produce epigenetic reprogramming, so that affected cells and tissues alter functioning, leading to morbidity and premature mortality. Epigenetic changes in the germ line can produce transgenerational, inherited gene regulatory changes. Within an individual lifespan, altered gene regulation via hyper- or hypo-methylation, acetylation, and the action of endogenous genetic elements leads to aging and growth abnormalities, including cancer, immune dysfunction, and cardiovascular disease.
Keywords
Attention Deficit Hyperactivity Disorder Attention Deficit Hyperactivity Disorder Epigenetic Change Endocrine Disruptor Allostatic LoadReferences
- Angelopoulou, R., Lavranos, G., & Manolakou, P. (2012). Sex determination strategies in 2012: Towards a common regulatory model? Reproductive Biology and Endocrinology, 10, 13. doi: 10.1186/1477-7827-10-13.PubMedCentralPubMedCrossRefGoogle Scholar
- Bauer, S. E., Wagner, S. E., Burch, J., Bayakly, R., & Vena, J. E. (2013). A case-referent study: Light at night and breast cancer risk in Georgia. International Journal of Health Geographics, 12, 23. doi: 10.1186/1476-072X-12-23.PubMedCentralPubMedCrossRefGoogle Scholar
- Blazkova, J., Trejbalova, K., Gondois-Rey, F., Halfon, P., Philibert, P., Guiguen, A., et al. (2009). CpG methylation controls reactivation of HIV from latency. PLOS Pathogens, 5(8), e1000554. doi: 10.1371/journal.ppat.1000554.PubMedCentralPubMedCrossRefGoogle Scholar
- Brunk, U. T., & Terman, A. (2002). The mitochondrial-lysosomal axis theory of aging: Accumulation of damaged mitochondria as a result of imperfect autophagocytosis. European Journal of Biochemistry, 269, 1996–2002.PubMedCrossRefGoogle Scholar
- Campbell, K. H. S., McWhir, J., Ritchie, W. A., & Wilmut, I. (1996). Sheep cloned by nuclear transfer from a cultured cell line. Nature, 380, 64–66.PubMedCrossRefGoogle Scholar
- Carson, R. (1962). Silent spring. Boston: Houghton Mifflin.Google Scholar
- Christensen, B. C., Houseman, E. A., Marsit, C. J., Zheng, S., Wrensch, M. R., Wiemels, J. L., et al. (2009). Aging and environmental exposures alter tissue-specific DNA methylation dependent upon CpG island context. PLOS Genetics, 5(8), e1000602. doi: 10.1371/journal.pgen.1000602.PubMedCentralPubMedCrossRefGoogle Scholar
- Christian, J. J., & Davis, D. E. (1964). Endocrines, behavior, and population. Science, 146(3651), 1550–1560.PubMedCrossRefGoogle Scholar
- Clark, S. J. (2007). Action at a distance: Epigenetic silencing of large chromosomal regions in carcinogenesis. Human Molecular Genetics, 16, R88–R95.PubMedCrossRefGoogle Scholar
- Cui, W., & Wang, L.-H. (2008). DNA methylation: A two-edged sword as a target for anti-cancer drugs. Bioscience Hypotheses, 1(6), 334–335.CrossRefGoogle Scholar
- Davies, P. C. W., Demetrius, L., & Tuszynski, J. A. (2011). Cancer as a dynamical phase transition. Theoretical Biology and Medical Modeling, 8, 30. doi: 10.1186/1742-4682-8-30.CrossRefGoogle Scholar
- Deppe, U., Schierenberg, E., Cole, T., Krieg, C., Schmitt, D., Yoder, B., et al. (1978). Cell lineages of the embryo of the nematode Caenorhabditis elegans. Proceedings of the National Academy of Sciences of the United States of America, 75, 376–380.PubMedCentralPubMedCrossRefGoogle Scholar
- Dixon, J. R., Jung, I., Selvaraj, S., Shen, Y., Antosiewicz-Bourget, J. E., Lee, A. Y., et al. (2015). Chromatin architecture reorganization during stem cell differentiation. Nature, 518, 331–336.PubMedCentralPubMedCrossRefGoogle Scholar
- Eckhardt, F., Lewin, J., Cortese, R., Rakyan, V. K., Attwood, J., Burger, M., et al. (2006). DNA methylation profiling of human chromosomes 6, 20, and 22. Nature Genetics, 38(12), 1378–1385.PubMedCentralPubMedCrossRefGoogle Scholar
- Eriksen, E. F., Axelrod, D. W., & Melsen, F. (1994). Bone histomorphometry. New York: Raven Press.Google Scholar
- Feinberg, A. P., & Irizarry, R. A. (2010). Stochastic epigenetic variation as a driving force of development, evolutionary adaptation, and disease. Proceedings of the National Academy of Sciences of the United States of America, 107(Suppl 1), 1757–1764.PubMedCentralPubMedCrossRefGoogle Scholar
- Ferrell, J. E. (2012). Bistability, bifurcations, and Waddington’s epigenetic landscape. Current Biology, 22(11), R458–R466.PubMedCentralPubMedCrossRefGoogle Scholar
- Fontana, L. (2008). Caloric restriction and cardiometabolic health. European Journal of Cardiovascular Prevention and Rehabilitation, 15(1), 3–9.PubMedCrossRefGoogle Scholar
- Frago, M. F., Ballestar, E., Paz, M. F., Ropero, S., Setien, F., Ballestar, M. L., et al. (2005). Epigenetic differences arise during the lifetime of monozygotic twins. Proceedings of the National Academy of Sciences of the United States of America, 102(30), 10604–10609.CrossRefGoogle Scholar
- Galvão, V., Miranda, J. G. V., Andrade, R. F. S., Andrade, J. S., Gallos, L. K., & Makse, H. A. (2010). Modularity maps of the network of human cell differentiation. Proceedings of the National Academy of Sciences of the United States of America, 107(13), 5750–5755.PubMedCentralPubMedCrossRefGoogle Scholar
- Gjoneska, E., Pfenning, A. R., Mathys, H., Quon, G., Kundaje, A., Tsai, L.-H., et al. (2015). Conserved epigenomic signals in mice and humans reveal immune basis of Alzheimer’s disease. Nature, 518, 365–369.PubMedCentralPubMedCrossRefGoogle Scholar
- Gluckman, P. D., Hanson, M. A., Buklijas, T., Low, F. M., & Beedle, A. S. (2009). Epigenetic mechanisms that underpin metabolic and cardiovascular diseases. Nature Reviews Endocrinology, 5, 401–408.PubMedCrossRefGoogle Scholar
- Godfray, H. C. J., Blacquiere, T., Field, L. M., Hails, R. S., Petrokofsky, G., Potts, S. G., et al. (2014). A restatement of the natural science evidence base concerning neonicotinoid insecticides and insect pollinators. Proceedings of the Royal Society B, 281, 20140558. doi: 10.1098/rspb.2014.0558.PubMedCentralPubMedCrossRefGoogle Scholar
- Goldberg, A. D., Allis, C. D., & Bernstein, E. (2007). Epigenetics: A landscape takes shape. Cell, 128, 635–638.PubMedCrossRefGoogle Scholar
- Gray, J., Nudelman, J., & Engel, C. (2010). State of the evidence: The connection between breast cancer and the environment, from science to action (6th ed.). San Francisco: Breast Cancer Fund. Accessed July 19, 2015, from www.breastcancerfund.org
- Guerrero-Bosagna, C. M., & Skinner, M. K. (2014). Environmental epigenetics and phytoestrogen/phytochemical exposures. Journal of Steroid Biochemistry and Molecular Biology, 139, 270–276.PubMedCrossRefGoogle Scholar
- Gurdon, J. B. (1960). The developmental capacity of nuclei taken from differentiating endoderm cells of Xenopus laevis. Journal of Embryology and Experimental Morphology, 8, 505–526.PubMedGoogle Scholar
- Gurdon, J. B. (1981). Molecular mechanisms in the control of gene expression during development. Biochemical Society Transactions, 9(1), 13–21.PubMedCrossRefGoogle Scholar
- Gurdon, J. B., Elsdale, T. R., & Fischberg, M. (1958). Sexually mature individuals of Xenopus laevis derived from the transplantation of single somatic nuclei. Nature, 182, 64–65.PubMedCrossRefGoogle Scholar
- Hadorn, E. (1965). Problems of determination and transdetermination. Brookhaven Symposium on Biology, 18, 148–161.Google Scholar
- Hadrich, C. M. (2011). Genetic variation and epigenetic patterns in autoimmunity. Journal of Genetic Syndromes and Gene Therapy, 2, 1. doi: 10.4172/2157-7412.10000e2.Google Scholar
- Halley-Stott, R. P., & Gurdon, J. B. (2013). Epigenetic memory in the context of nuclear reprogramming and cancer. Briefings in Functional Genomics, 12(3), 164–173.PubMedCentralPubMedCrossRefGoogle Scholar
- Harvey, S. A., & Smith, J. C. (2009). Visualization and quantification of morphogen gradient formation in the zebrafish. PLOS Biology, 7(5), e1000101. doi: 10.1371/journal.pbio.1000101.PubMedCentralPubMedCrossRefGoogle Scholar
- Hayflick, L. (2007a). Biological aging is no longer an unsolved problem. Annals of the New York Academy of Sciences, 1100, 1–13.PubMedCrossRefGoogle Scholar
- Hayflick, L. (2007b). Entropy explains aging, genetic determinism explains longevity, and undefined terminology explains misunderstanding both. PLOS Genetics, 3(12), 2351–2354.CrossRefGoogle Scholar
- Heijmans, B. T., Tobi, E. W., Stein, A. D., Putter, H., Blauw, G. J., Susser, E. S., et al. (2008). Persistent epigenetic differences associated with prenatal exposures to famine in humans. Proceedings of the National Academy of Sciences of the United States of America, 105(44), 17046–17049.PubMedCentralPubMedCrossRefGoogle Scholar
- Henke, C., Reubner, M., Faschingbauer, F., Stolt, C. C., Schaefer, N., Lang, N., et al. (2013). Regulation of murine placentogenesis by the retroviral genes Syncytin-A, Syncytin-B and Peg10. Differentiation, 85, 150–160.PubMedCrossRefGoogle Scholar
- Hollar, D. (2012). Development from conception through adolescence: Physiological and psychosocial factors impacting children with special health care needs. In D. Hollar (Ed.), Handbook of children with special health care needs (pp. 289–306). New York: Springer.CrossRefGoogle Scholar
- Hollar, D. (2013). Cross-sectional patterns of allostatic load among persons with varying disabilities, NHANES: 2001–2010. Disability and Health Journal, 6, 177–187.PubMedCrossRefGoogle Scholar
- Hollar, D., & Lewis, J. (2015). Heart age differentials and general cardiovascular risk profiles for persons with varying disabilities: NHANES 2001–2010. Disability and Health Journal, 8, 51–60.PubMedCrossRefGoogle Scholar
- Jacob, F., & Monod, J. (1961). Genetic regulatory mechanisms in the synthesis of proteins. Journal of Molecular Biology, 3(3), 318–356.PubMedCrossRefGoogle Scholar
- Johnson, L. J., & Tricker, P. J. (2010). Epigenomic plasticity within populations: Its evolutionary significance and potential. Heredity, 105, 113–121.PubMedCrossRefGoogle Scholar
- Kabasenche, W. P., & Skinner, M. K. (2014). DDT, epigenetic harm, and transgenerational environmental justice. Environmental Health, 13, 62. doi: 10.1186/1476-069X-13-62.PubMedCentralPubMedCrossRefGoogle Scholar
- Kelly, T., & Jones, P. (2010). DAMD to epigenetic silence. Proceedings of the National Academy of Sciences of the United States of America, 107(1), 3–4.PubMedCentralPubMedCrossRefGoogle Scholar
- Kiefer, J. C. (2007). Epigenetics in development. Developmental Dynamics, 236, 1144–1156.PubMedCrossRefGoogle Scholar
- Kothapalli, C. R., Taylor, P. M., Smolenski, R. T., Yacoub, M. H., & Ramamurthi, A. (2009). Transforming growth factor beta 1 and hyaluronan oligomers synergistically enhance elastin matrix regeneration by vascular smooth muscle cells. Tissue Engineering, Part A, 15(3), 501–511.CrossRefGoogle Scholar
- La Merrill, M., Cirillo, P. M., Terry, M. B., Krigbaum, N. Y., Flom, J. D., & Cohn, B. A. (2013). Prenatal exposure to the pesticide DDT and hypertension diagnosed in women before age 50: A longitudinal birth cohort study. Environmental Health Perspectives, 121, 594–599.PubMedCentralPubMedGoogle Scholar
- Laskey, R. A., & Gurdon, J. B. (1970). Genetic content of adult somatic cells tested by nuclear transplantation from cultured cells. Nature, 228, 1332–1334.PubMedCrossRefGoogle Scholar
- Leopold, A. (1949). A sand county almanac. New York: Oxford University Press.Google Scholar
- Löwer, R., Löwer, J., & Kurth, R. (1996). The viruses in all of us: Characteristics and biological significance of human endogenous retrovirus sequences. Proceedings of the National Academy of Sciences of the United States of America, 93, 5177–5184.PubMedCentralPubMedCrossRefGoogle Scholar
- Manikkam, M., Guerrero-Bosagna, C., Tracey, R., Haque, M. M., & Skinner, M. K. (2012). Transgenerational actions of environmental compounds on reproductive disease and identification of epigenetic biomarkers of ancestral exposures. PLOS One, 7(2), e31901. doi: 10.1371/journal.pone.0031901.PubMedCentralPubMedCrossRefGoogle Scholar
- Melo, S. A., & Esteller, M. (2011). A precursor microRNA in a cancer cell nucleus: Get me out of here! Cell Cycle, 10(6), 922–925.PubMedCentralPubMedCrossRefGoogle Scholar
- Melo, S. A., & Esteller, M. (2014). Disruption of microRNA nuclear transport in human cancer. Seminars in Cancer Biology, 27, 46–51.PubMedCrossRefGoogle Scholar
- Mercer, T. R., Dinger, M. E., & Mattick, J. S. (2009). Long non-coding RNAs: Insights into functions. Nature Reviews Genetics, 10, 155–159.PubMedCrossRefGoogle Scholar
- Mintz, B., & Illmensee, K. (1975). Normal genetically mosaic mice produced from malignant teratocarcinoma cells. Proceedings of the National Academy of Sciences of the United States of America, 72(9), 3585–3589.PubMedCentralPubMedCrossRefGoogle Scholar
- Mnif, W., Hassine, A. I. H., Bouaziz, A., Bartegi, A., Thomas, O., & Roig, B. (2011). Effect of endocrine disruptor pesticides: A review. International Journal of Environmental Research and Public Health, 8, 2265–2303.PubMedCentralPubMedCrossRefGoogle Scholar
- Morgan, H. D., Santos, F., Green, K., Dean, W., & Reik, W. (2005). Epigenetic reprogramming in mammals. Human Molecular Genetics, 14(1), R47–R58.PubMedCrossRefGoogle Scholar
- Mori, C. (2004). High-risk group and high-risk life stage: Key issues in adverse effects of environmental agents on human health. Reproductive Medicine and Biology, 3, 51–58.CrossRefGoogle Scholar
- Muller, P. H. (1946). Über zusammenhänge zwischen Konstitution und insectizider Wirkung. Helvetica Chimica Acta, 29, 1560–1580.Google Scholar
- Mullin, C. A., Frazier, M., Frazier, J. L., Ashcroft, S., Simonds, R., van Engelsdorp, D., et al. (2010). High levels of miticides and agrochemicals in North American apiaries: Implications for honey bee health. PLOS One, 5(3), e9754. doi: 10.1371/journal.pone.0009754.PubMedCentralPubMedCrossRefGoogle Scholar
- National Center for Health Statistics. (2012). Healthy people 2010 final review: Progress charts. Hyattsville, MD: U.S. Department of Health and Human Services, Centers for Disease Control and Prevention (PHS Publication No. 2012–1039).Google Scholar
- Parle-McDermott, A., & Ozaki, M. (2011). The impact of nutrition on differential methylated regions of the genome. Advances in Nutrition, 2, 463–471.PubMedCentralPubMedCrossRefGoogle Scholar
- Pearson, J. C., Lemons, D., & McGinnis, W. (2005). Modulating Hox gene functions during animal body patterning. Nature Reviews Genetics, 6, 893–904.PubMedCrossRefGoogle Scholar
- Pembrey, M. E., Bygren, L. O., Kaati, G., Edvinsson, S., Northstone, K., Sjostrom, M., et al. (2006). Sex-specific, male-line transgenerational responses in humans. European Journal of Human Genetics, 14, 159–166.PubMedCrossRefGoogle Scholar
- Petronis, A. (2010). Epigenetics as a unifying principle in the aetiology of complex traits and diseases. Nature, 465, 721–727.PubMedCrossRefGoogle Scholar
- Pogribny, I. P., & Vanyushin, B. F. (2010). Age-related genomic hypomethylation. In T. O. Tollefsbol (Ed.), Epigenetics of aging (pp. 11–28). New York: Springer.CrossRefGoogle Scholar
- Prigogine, I. (1977). Time, structure, and fluctuations. Stockholm: The Nobel Foundation.Google Scholar
- Prigogine, I. (2002). Dynamical roots of time symmetry breaking. Philosophical Transactions of the Royal Society of London A, 360, 299–301.CrossRefGoogle Scholar
- Radtke, K. M., Ruf, M., Gunter, H. M., Dohrmann, K., Schauer, M., Meyer, A., et al. (2011). Transgenerational impact of intimate partner violence on methylation in the promoter of the glucocorticoid receptor. Translational Psychiatry, 1, e21. doi: 10.1038/tp.2011.21.PubMedCentralPubMedCrossRefGoogle Scholar
- Raine, N. E., & Gill, R. J. (2015). Tasteless pesticides affect bees in the field. Nature, 521, 38–40.PubMedCrossRefGoogle Scholar
- Reiter, R. J., Tan, D. X., Korkmaz, A., & Rosales-Corral, S. A. (2014). Melatonin and stable circadian rhythms optimize maternal, placental and fetal physiology. Human Reproduction Update, 20(2), 293–307.PubMedCrossRefGoogle Scholar
- Roadmap Epigenomics Consortium, Kundaje, A., Meuleman, W., Ernst, J., Bilenky, M., Yen, A., et al. (2010). Integrative analysis of 111 reference human epigenomes. Nature, 518, 317–330.Google Scholar
- Roberts, T. C. (2014). The microRNA biology of the mammalian nucleus. Molecular Therapy – Nucleic Acids, 3(8), e188. doi: 10.1038/mtna.2014.40.PubMedCentralPubMedCrossRefGoogle Scholar
- Rong, J. X., Shapiro, M., Trogan, E., & Fisher, E. A. (2003). Transdifferentiation of mouse aortic smooth muscle cells to a macrophage-like state after cholesterol loading. Proceedings of the National Academy of Sciences of the United States of America, 100(23), 13531–13536.PubMedCentralPubMedCrossRefGoogle Scholar
- Roth, T. L., & Sweatt, J. D. (2011). Annual research review: Epigenetic mechanisms and environmental shaping of the brain during sensitive periods of development. Journal of Child Psychology and Psychiatry, 52(4), 398–408.PubMedCentralPubMedCrossRefGoogle Scholar
- Seeman, T. E., McEwen, B. S., Rowe, J. W., & Singer, B. H. (2001). Allostatic load as a marker of cumulative biological risk: MacArthur studies of successful aging. Proceedings of the National Academy of Sciences of the United States of America, 98(8), 4770–4775.PubMedCentralPubMedCrossRefGoogle Scholar
- Seeman, T. E., Singer, B. H., Ryff, C. D., Love, G. D., & Levy-Storms, L. (2002). Social relationships, gender, and allostatic load across two age cohorts. Psychosomatic Medicine, 64, 395–406.PubMedCrossRefGoogle Scholar
- Selye, H. (1950). Stress and the general adaptation syndrome. The British Medical Journal, 1(4667), 1382–1392.CrossRefGoogle Scholar
- Shen, L., Catalano, P. J., Benson, A. B., O’Dwyer, P., Hamilton, S. R., & Issa, J. P. J. (2007). Association between DNA methylation and shortened survival in patients with advanced colorectal cancer treated with 5-fluorouracil-based chemotherapy. Clinical Cancer Research, 13(20), 6093–6098.PubMedCentralPubMedCrossRefGoogle Scholar
- Shiraishi, M., Oates, A. J., & Sekiya, T. (2002). An overview of the analysis of DNA methylation in mammalian genomes. Biological Chemistry, 383(6), 893–906.PubMedCrossRefGoogle Scholar
- Skinner, M. K., Manikkam, M., & Guerrero-Bosagna, C. (2011). Epigenetic transgenerational actions of endocrine disruptors. Reproductive Toxicology, 31(3), 337–343.PubMedCentralPubMedCrossRefGoogle Scholar
- Stevens, L. C. (1960). Embryonic potency of embryoid bodies derived from a transplantable testicular teratoma of the mouse. Developmental Biology, 2, 285–297.PubMedCrossRefGoogle Scholar
- Stevens, L. C. (1973). A developmental genetic approach to the study of teratocarcinogenesis. BioScience, 23(3), 169–172.CrossRefGoogle Scholar
- Symonds, M. E. (2010). Epigenomics – grand challenge: Much more than the developmental origins of adult health and disease. Frontiers in Genetics, 1, 1. doi: 10.3389/fgene.2010.00001.PubMedCentralPubMedCrossRefGoogle Scholar
- Takeuchi, J. K., & Bruneau, B. G. (2009). Directed transdifferentiation of mouse mesoderm to heart tissue by defined factors. Nature, 459, 708–712.PubMedCentralPubMedCrossRefGoogle Scholar
- Taruscio, D., & Mantovani, A. (1998). Human endogenous retroviral sequences: Possible roles in reproductive physiopathology. Biology of Reproduction, 59, 713–724.PubMedCrossRefGoogle Scholar
- Thom, R. (1972). Structural stability and morphogenesis. New York: W. A. Benjamin.Google Scholar
- Tren, R. (2010). DDT and malaria prevention. Environmental Health Perspectives, 118(1), A14–A15.PubMedCentralPubMedGoogle Scholar
- U.S. Environmental Protection Agency. (2013). America’s children and the environment (3rd ed.). Washington, DC: Author (Publication No. EPA 240-R-13-001).Google Scholar
- van den Berg, H. (2009). Global status of DDT and its alternatives for use in vector control to prevent disease. Environmental Health Perspectives, 117, 1656–1663.PubMedCentralPubMedCrossRefGoogle Scholar
- Van der Muelen, J., Speleman, F., & Van Vlierberghe, P. (2014). The H3K27me3 demethylase UTX in normal development and disease. Epigenetics, 9(5), 658–668.CrossRefGoogle Scholar
- Waddington, C. H. (1957). The strategy of the genes: A discussion of some aspects of theoretical biology. London: Allen & Unwin.Google Scholar
- Waterland, R. A., Kellermayer, R., Rached, M.-T., Taterian, N., Gomes, M. V., Zhang, J., et al. (2009). Epigenomic profiling indicates a role for DNA methylation in early postnatal liver development. Human Molecular Genetics, 18(16), 3026–3028.PubMedCentralPubMedCrossRefGoogle Scholar
- Wilkins, A. S. (2010). The enemy within: An epigenetic role of retrotransposons in cancer initiation. Bioessays, 32, 856–865.PubMedCrossRefGoogle Scholar
- Wilson, E. O. (1984). Biophilia: The human bond with other species. Cambridge, MA: Harvard University Press.Google Scholar
- Wolpert, L., Beddington, R., Brockes, J., Jessell, T., Laurence, P., & Meyerowitz, E. (1998). Principles of development. New York: Oxford University Press.Google Scholar
- Ye, M., Beach, J., Martin, J. W., & Senthilselvan, A. (2015). Association between lung function in adults and plasma DDT and DDE levels: Results from the Canadian Health Measures Survey. Environmental Health Perspectives, 123(5), 422–427.PubMedCentralPubMedGoogle Scholar
- Yehuda, R., & Bierer, L. (2009). The relevance of epigenetics to PTSD: Implications for the DSM-IV. Journal of Trauma and Stress, 22(5), 427–434.CrossRefGoogle Scholar
- Yu, W., Gins, D., Onyango, P., Muldoon-Jacobs, K., Karp, J., Feinberg, A. P., et al. (2008). Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA. Nature, 451, 202–206.PubMedCentralPubMedCrossRefGoogle Scholar
- Zamudio, N., & Bourc’his, D. (2010). Transposable elements in the mammalian germline: A comfortable niche or a deadly trap? Heredity, 105, 92–104.PubMedCrossRefGoogle Scholar
- Zhong, S.-H., Liu, J.-Z., Jin, H., Lin, L., Li, Q., Chen, Y., et al. (2013). Warm temperatures induce transgenerational epigenetic release of RNA silencing by inhibiting siRNA biogenesis in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America, 110(22), 9171–9176.PubMedCentralPubMedCrossRefGoogle Scholar
- Zucchi, F. C. R., Yao, Y., & Metz, G. A. (2012). The secret language of destiny: Stress imprinting and transgenerational origins of disease. Frontiers in Genetics, 3, 96. doi: 10.3389/fgene.2012.00096.PubMedCentralPubMedCrossRefGoogle Scholar