
Real life by definition combines heritability (e.g., the legacy of exposures) and experience (e.g. stress during sensitive or 'critical' periods), but how to study or even model this interaction has proven difficult. The hoary concept of evaluating traits according to nature versus nurture continues to persist despite repeated demonstrations that it retards, rather than advances, our understanding of biological processes. Behavioral genetics has proven the obvious, that genes influence behavior and, vice versa, that behavior influences genes. The concept of Genes X Environment (G X E) and its modern variants was viewed as an improvement on nature-nurture but has proven that, except in rare instances, it is not possible to fractionate phenotypes into these constituent elements. The entanglement inherent in terms such as nature-nurture or G X E is a Gordian knot that cannot be dissected or even split. Given that the world today is not what it was less than a century ago, yet the arbitrator (differential survival and reproduction) has stayed constant, de novo principles and practices are needed to better predict what the future holds. Put simply, the transformation that is now occurring within and between individuals as a product of global endocrine disruption is quite independent of what has been regarded as evolution by selection. This new perspective should focus on how epigenetic modifications might revise approaches to understand how the phenotype and, in particular its components, is shaped. In this review we summarize the literature in this developing area, focusing on our research on the fungicide vinclozolin.
Male, 570, Gene Expression, Endocrine Disruptors, Environment, Endocrine Disruptors - adverse effects, Oxazoles - adverse effects, Epigenesis, Genetic, Rats, Sprague-Dawley, Animals, Humans, Genetic Predisposition to Disease, Oxazoles, Fungicides, Industrial - adverse effects, DNA Methylation - genetics, Androgen Antagonists, Environmental Exposure, DNA Methylation, Fungicides, Industrial, Rats, Corticosterone - blood, Epigenetics, Female, Gene-Environment Interaction, Sprague-Dawley, Androgen Antagonists - adverse effects, Corticosterone
Male, 570, Gene Expression, Endocrine Disruptors, Environment, Endocrine Disruptors - adverse effects, Oxazoles - adverse effects, Epigenesis, Genetic, Rats, Sprague-Dawley, Animals, Humans, Genetic Predisposition to Disease, Oxazoles, Fungicides, Industrial - adverse effects, DNA Methylation - genetics, Androgen Antagonists, Environmental Exposure, DNA Methylation, Fungicides, Industrial, Rats, Corticosterone - blood, Epigenetics, Female, Gene-Environment Interaction, Sprague-Dawley, Androgen Antagonists - adverse effects, Corticosterone
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 68 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
