both on and off genes are designed to help the body, but when certain changes happen through dna methylation, specific genes that cause harm could be turned on, leading to chronic diseases. in some cases, turning off genes can lead to improper functions that drive the onset of health issues.
the affected genes are part of the epigenome, which is the term used to describe a grouping of chemical modifications that regulate how genes express themselves and, how genes are used and when. the epigenome does not alter the dna sequence. typically, this epigenome is designed to be fluid throughout one’s life so that any necessary changes to respond to environmental or psychosocial stressors, such as traumatic events, can occur freely.
dr. mulligan and her team found that changes to dna and gene expression in the epigenome in mothers who experience trauma can affect both their unborn children and grandchildren as those changed genes develop in the fetus. this led to prenatal and germline effects due to dna and gene expression.
“when the women were pregnant, they experienced the trauma directly. their developing baby experienced it prenatally, and then the oocytes in their developing baby experienced the violence through a germline exposure,” said dr. mulligan. “so, in other words, all three generations were exposed to the violence in one sense or another.”
she goes on to note that these marks on the epigenome in mothers are so significant that “you don’t even have to directly experience violence to have it leave a mark.”
what this means for children of trauma survivors
with biological changes, dna, and gene expression being the cornerstones of cellular function, adaptation to changing environments, and overall health, scientists are now able to observe how these changes can be passed down to unborn children and grandchildren. this paves the way for understanding how intergenerational trauma can affect even those who did not directly experience the original traumatic event.