Title:Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress
VOLUME: 19 ISSUE: 8
Author(s):Ludwig Stenz, Daniel S. Schechter*, Sandra Rusconi Serpa and Ariane Paoloni-Giacobino
Affiliation:Department of Genetic Medicine and Development, University of Geneva Hospitals and Faculty of Medicine, Geneva, Department of Child & Adolescent Psychiatry, University of Geneva Hospitals and Faculty of Medicine, Geneva, Department of Child & Adolescent Psychiatry, University of Geneva Hospitals and Faculty of Medicine, Geneva, Department of Genetic Medicine and Development, University of Geneva Hospitals and Faculty of Medicine, Geneva
Keywords:Intergenerational, Transmission, DNA methylation, ELS, Early life stress, HPA.
Abstract:Early life stress in humans (i.e. maltreatment, violence exposure, loss of a loved one) and in rodents
(i.e. disrupted attachment or nesting, electric shock, restraint, predator odor) occurs during critical
steps of neural circuit formation. ELS in humans is associated with increased risk for developmental psychopathology,
including anxious and depressive phenotypes. The biological mechanisms underlying these
potentially persistent maladaptive changes involve long-term epigenetic modifications, which have been
suggested to be potentially transmissible to subsequent generations. DNA methylation is an epigenetic
mechanism that modifies gene expression patterns in response to environmental challenges and influences
mutation rates. It remains to be seen whether a functionally relevant fraction of DNA methylation marks can
escape genome-wide erasures that occur in primordial germ cells and after fertilization within the zygote.
Early life-stress-triggered changes in epigenetic mediated transmission of acquired behavioral traits among
humans have been assessed mainly by targeting genes involved in the hypothalamic-pituitary-adrenal
(HPA) axis, such as NR3C1 and FKBP5. Recently, researchers examining epigenetic transmission have begun
to apply genome-wide approaches. In humans, reduced representation bisulfite sequencing (RRBS) was
performed on peripheral samples that were obtained from individuals who were prenatally exposed to the
“Dutch Hunger Winter”, resulting in two Differentially Methylated Regions (DMRs) in INSR and CPTIA
genes that were functionally, biologically and technically validated, and significantly associated with birth
weights and LDL cholesterol levels in offspring. In rodents, non-genomic intergenerational transmission of
anxiety which was associated with differentially methylated enhancers that were putatively involved in lipid
signaling and synaptic/neurotransmission in hippocampal granule cells, was discovered also using RRBS.
Finally, transgenerational transmission of altered behaviors was associated with sperm-derived microRNAs
produced by ELS male mice. The field of epigenetic transmission is just beginning to enter the epigenomic
era by using genome-wide analyses. Such approaches remain of strong interest to human studies, first in order
to help to assess the relevance of the previous targeted studies, and second to discover new important
epigenetic modifications of potential clinical importance. New discoveries may help to assess how transmittable
the negative impact of stress may be to offspring. The latter may open doors for future treatments and
resilience-promoting interventions, as well as new approaches to treat the effects of childhood trauma before
the onset of psychiatric disorder.
