Nce for transgenerational epigenetic inheritance comes from studies in plants and

Nce for transgenerational epigenetic inheritance comes from studies in plants and mice [140?43]. In the dandelion, exogenous stress induces changes in DNA methylation that are transmitted to the next generation [141?43]. In the mouse, the Avy locus, a gene region that controls coat color, can be epigenetically modified by environmental exposures such as diet [142]. These epigenetic modifications can be transgenerationally inherited and influence phenotypes in the offspring [140,142], suggesting that there is a failure to erase the epigenetic marks that are established at the Avy locus in the germline. The epigenetic marks that facilitate transgenerational epigenetic inheritance are poorly understood [144]. The simplest explanation has always been that DNA methylation at specific loci escapes the reprogramming events. But how? One possible mechanism might involve retrotransposons, as these DNA repeat elements seem to be resistant to the erasure of DNA methylation patterns during reprogramming [143?47]. In fact, the Avy locus is actually a retrotransposon inserted upstream of the transcription start site of the Agouti gene. Additionally, recent work in Caenorhabditis elegans suggests that epigenetic marks, such as histone H3 lysine 4 trimethylation could mediate transgenerational inheritance [148?50]. The recent discovery that germline cells contain large numbers of small RNA species suggests another novel way of transmitting epigenetic information through the germ line [143,144,151,152]. Research has shown that the OPC-8212 site maternal transmission of piwi-interacting RNAs (piRNAs) in Drosophila influences fertility of offspring via piRNA-directed silencingAuthor PF-04418948 chemical information Manuscript Author Manuscript Author Manuscript Author ManuscriptSemin Oncol. Author manuscript; available in PMC 2017 February 01.Ryan and Faupel-BadgerPageof transposable elements [143,153]. Recent work also demonstrated that early developmental trauma in mice leads to behavioral and metabolic changes that are inherited in offspring for several generations [143,154]. These phenotypes were conveyed to the offspring by miRNAs and piwiRNAs in the sperm [154]. The relevance of this observation to cancer is apparent when one considers that cigarette smoking induces differential miRNA expression in human spermatozoa [155], perhaps suggesting one mechanism by which tobacco exposure can influence not just the cancer risk of the exposed individual, but also that of the offspring. One of the earliest examples of transgenerational inheritance of traits in humans was in 2001 when a Swedish study found that the nutritional and smoking habits of paternal grandparents could influence their descendants’ lifespan [156]. In addition, prenatal exposure–especially around the time of conception–to famine during the Dutch Hunger Winter (1944-1945) led to hypomethylation at the IGF2 gene among offspring conceived at that time [157]. A key future area to explore will be to determine what the phenotypic effects of such exposures and epigenetic changes are. Recent experimental evidence shed light on a potential mechanism for this observation and may also involve transmission of small RNAs. Starvation was found to induce expression of specific RNAs that were then inherited across multiple generations, targeting genes involved in nutrition [158]. So, can the food we eat, the air we breathe and our emotional experiences impact the health and happiness of our descendants? [144] While studies undoubtedly show evidence.Nce for transgenerational epigenetic inheritance comes from studies in plants and mice [140?43]. In the dandelion, exogenous stress induces changes in DNA methylation that are transmitted to the next generation [141?43]. In the mouse, the Avy locus, a gene region that controls coat color, can be epigenetically modified by environmental exposures such as diet [142]. These epigenetic modifications can be transgenerationally inherited and influence phenotypes in the offspring [140,142], suggesting that there is a failure to erase the epigenetic marks that are established at the Avy locus in the germline. The epigenetic marks that facilitate transgenerational epigenetic inheritance are poorly understood [144]. The simplest explanation has always been that DNA methylation at specific loci escapes the reprogramming events. But how? One possible mechanism might involve retrotransposons, as these DNA repeat elements seem to be resistant to the erasure of DNA methylation patterns during reprogramming [143?47]. In fact, the Avy locus is actually a retrotransposon inserted upstream of the transcription start site of the Agouti gene. Additionally, recent work in Caenorhabditis elegans suggests that epigenetic marks, such as histone H3 lysine 4 trimethylation could mediate transgenerational inheritance [148?50]. The recent discovery that germline cells contain large numbers of small RNA species suggests another novel way of transmitting epigenetic information through the germ line [143,144,151,152]. Research has shown that the maternal transmission of piwi-interacting RNAs (piRNAs) in Drosophila influences fertility of offspring via piRNA-directed silencingAuthor Manuscript Author Manuscript Author Manuscript Author ManuscriptSemin Oncol. Author manuscript; available in PMC 2017 February 01.Ryan and Faupel-BadgerPageof transposable elements [143,153]. Recent work also demonstrated that early developmental trauma in mice leads to behavioral and metabolic changes that are inherited in offspring for several generations [143,154]. These phenotypes were conveyed to the offspring by miRNAs and piwiRNAs in the sperm [154]. The relevance of this observation to cancer is apparent when one considers that cigarette smoking induces differential miRNA expression in human spermatozoa [155], perhaps suggesting one mechanism by which tobacco exposure can influence not just the cancer risk of the exposed individual, but also that of the offspring. One of the earliest examples of transgenerational inheritance of traits in humans was in 2001 when a Swedish study found that the nutritional and smoking habits of paternal grandparents could influence their descendants’ lifespan [156]. In addition, prenatal exposure–especially around the time of conception–to famine during the Dutch Hunger Winter (1944-1945) led to hypomethylation at the IGF2 gene among offspring conceived at that time [157]. A key future area to explore will be to determine what the phenotypic effects of such exposures and epigenetic changes are. Recent experimental evidence shed light on a potential mechanism for this observation and may also involve transmission of small RNAs. Starvation was found to induce expression of specific RNAs that were then inherited across multiple generations, targeting genes involved in nutrition [158]. So, can the food we eat, the air we breathe and our emotional experiences impact the health and happiness of our descendants? [144] While studies undoubtedly show evidence.