Transgenerational inheritance of fetal alcohol effects on proopiomelanocortin gene expression and methylation, cortisol response to stress, and anxiety-like behaviors in offspring for three generations in rats: Evidence for male germline transmission

Abstract

Previously it has been shown that fetal alcohol exposure increases the stress response partly due to lowering stress regulatory proopiomelanocortin (Pomc) gene expression in the hypothalamus via epigenetic mechanisms for multiple generations in mixed-breed rats. In this study we assess the induction of heritable epigenetic changes of Pomc-related variants by fetal alcohol exposure in isogenic Fischer 344 rats. Using transgenerational breeding models and fetal alcohol exposure procedures, we determined changes in hypothalamic Pomc gene expression and its methylation levels, plasma corticosterone hormone response to restraint stress, and anxiety-like behaviors using elevated plus maze tests in fetal alcohol-exposed offspring for multiple generations in isogenic Fischer rats. Fetal alcohol-exposed male and female rat offspring showed significant deficits in POMC neuronal functions with increased Pomc gene methylation and reduced expression. These changes in POMC neuronal functions were associated with increased plasma corticosterone response to restraint stress and increased anxiety-like behavior. These effects of fetal alcohol exposure persisted in the F1, F2, and F3 progeny of the male germline but not of the female germline. These data suggest that fetal alcohol exposure induces heritable changes in Pomc-related variants involving stress hyperresponsiveness and anxiety-like behaviors which perpetuate into subsequent generations through the male germline via epigenetic modifications.

About the Authors:

Omkaram Gangisetty

Roles Conceptualization, Data curation, Formal analysis, Writing – review & editing

Affiliation: Rutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America

Shaista Chaudhary

Roles Data curation, Formal analysis, Investigation, Writing – review & editing

Affiliation: Rutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America

Ajay Palagani

Roles Data curation, Formal analysis, Investigation

Affiliation: Rutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America

Dipak K. Sarkar

Roles Conceptualization, Funding acquisition, Writing – original draft

* E-mail: [email protected]

Affiliation: Rutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America

ORCID logo https://orcid.org/0000-0003-3237-9871

Introduction

The transgenerational effect of environmental toxicants was first demonstrated in rodent models in 2005 [1]. We are the first to demonstrate the transgenerational effects of alcohol in a rodent model of fetal alcohol exposure (FAE) [2]. Since then, transgenerational effects of alcohol and other drugs and stress during the developmental period have been demonstrated by many laboratories using rodent models [3–9]. Also, male-germline-mediated transgenerational transmission has been demonstrated for maternal diet effects through the F3 generation [10]. Transgenerational effects refer to phenomena that could not be ascribed to direct exposure of the target or stimulant on the affected organism. For instance, it can only affect the gestating embryo results in the altered phenotype in the second or third generation either through male or female transmission. However, the intergenerational effects occur when maternal exposure has direct effects on the altered phenotype of F1 and possibly on F2 offspring. Some human genetic studies provide evidence of intergenerational transmission of risk variants with the paternal lineage [11–13]. Additionally, sex-chromosome-wide association analysis suggested male-specific risk genes for alcohol dependence [14]. Transgenerational occurrence of reproductive diseases that have been linked to endocrine disruptors and endometriosis in women has also been documented [15]. Data of the Avon Longitudinal Study of Parents and Children (ALSPAC) indicate an association of grand maternal smoking with increased birth weight, birth length, and BMI in grandsons of non-smoking mothers but not in granddaughters—evidence for possible transgenerational transmission through the male germline in humans [16]. Epidemiological studies have shown an association of paternal alcohol consumption with deficiencies in offspring, such as decreases in birth weight and increases in ventricular septal defects in children [17], effects which are typically found with maternal alcohol exposure [18]. There is evidence that hyperactivity and diminished cognitive abilities in some children are related biologically to an alcoholic father [19, 20]. Alcohol abuse in humans is also shown to cause demethylation of normally hypermethylated imprinted regions in sperm DNA that is proposed to alter critical gene expression required for normal prenatal development resulting in offspring with features of fetal alcohol spectrum disorders (FASD) [21]. Our recent study using a human cohort of the Collaborative Initiative on Fetal Alcohol Spectrum Disorders (CIFASD) identified higher DNA methylation of the proopiomelanocortin (POMC) gene, which regulates stress axis functions, in mothers (and in their children) who gave birth to children with fetal alcohol spectrum disorder [22]. These data support the notion that epigenetic mechanisms might be involved in transgenerational effects of alcohol. Previously, by employing outbred Sprague-Dawley rats, we demonstrated that the fetal alcohol exposure increases methylation of the Pomc gene in association with stress hyperresponse in offspring for multiple generations [2]. Epigenetic states can be influenced by an underlying DNA sequence or be purely epigenetic (sequence-independent) [23]. An unbiased assessment of the heritability of epigenetic variation requires working with isogenic populations, in which any genetic contribution to variations can be neglected. Studies have reported various gene promoter DNA methylation changes following ethanol exposure, including Slc6a4 (serotonin transporter), Slc17a6 (glutamate transporter), oxidative stress, and peroxisome biogenesis genes. In addition, prenatal ethanol exposure led to decreased promoter methylation of polycomb repressive complex 1 members and TATA-box binding protein associated factors. A common endophenotype of fetal alcohol-exposed offspring is an elevated response of the hypothalamic pituitary adrenal axis. POMC is a critical regulator of the hypothalamic pituitary adrenal axis. We therefore assessed the induction of heritable epigenetic Pomc-related variants by fetal alcohol exposure in isogenic Fischer 344 (F344) rats maintained in standardized conditions in order to control both genetic and environmental sources of variations. The data of this study indicate a significant increase in methylation levels in the proximal part of Pomc promoter with the concomitant reduction in Pomc mRNA levels, in association with enhancement of stress hormone response to a stress challenge and increased anxiety-like behaviors in F1, F2, or F3 male progeny of the alcohol-fed mother’s male lineage.

Materials and methods

Animals

All rat studies were performed with approved protocol (PROTO0999900285) in compliance with the Association for the Assessment and Accreditation of Laboratory Animal Care and Rutgers University. Fischer rats were obtained from Harlan Laboratories (Indianapolis, IN) and were housed in a controlled condition at a constant temperature of 22°C and 12-hour light/dark cycles throughout the study. These rats were bred in our animal facility and used for this study. On gestational day (GD) 7 through 21, rats were fed with rat chow ad libitum (AD), a liquid diet containing ethanol (AF; 1.7–5.0% v/v from GD7-10 and 6.7% v/v from GD11-21; Bioserve Inc., Frenchtown, NJ), or pair-fed (PF; Bioserve) an isocaloric liquid control diet (with alcohol calories replaced by maltose-dextrin). Previous studies have shown that the peak blood ethanol concentration is achieved in the range of 120–150 mg/dl in pregnant dams fed with this ethanol-containing liquid diet [24]. AF and PF litters were cross-fostered, and the litter size was maintained at 8 pups/dam. Only one pup from each litter was used in an experimental measure. Transgenerational studies were conducted by breeding AF, PF, or AD rats with control animals of the opposite gender to produce two germlines. We generated the male germline (AFM or PFM) by breeding male (AF or PF) rats and their male offspring with control (AD) female rats and the female germline (AFF or PFF) by breeding female (AF or PF) rats and their female offspring with control (AD) male rats. All rats were sacrificed by rapid decapitation to avoid stress at 60–90 days after birth, and tissues were collected for further experimentation.

Corticosterone response to restraint stress

Corticosterone response to restraint stress at various time points were determined in male and female rat offspring (on day of diestrus) at day 60 after birth from male and female germlines. Animals were restrained by placing them in a transparent plexiglass restrainer for 1 hour (between 12:00 and 14:00h). Blood samples were collected at various time points before (0h) and after restraint. Female rats were restrained on the day of diestrus to avoid the influence of the fluctuating levels of steroid on the corticosterone response. Plasma corticosterone levels were measured using corticosterone ELISA kit (IBL America, Mineopolis, MN) following manufacturer’s instructions.

Elevated plus maze

The elevated plus maze (EPM) test was conducted to assess anxiety-related behaviors as described previously [25]. The apparatus with a shape of a ‘‘+”consisted of two open arms and two closed arms. The arms extended from a central platform, 10 × 10 cm2 in area, and the maze was elevated to a height of 55 cm from the floor. Rats placed on the junction of the open and closed arms were allowed to freely explore the maze for 300 second. The time spent in the open and closed arms was recorded using ANY-Maze video tracking software. Proper care was taken to avoid any sudden noise or disturbance. The apparatus was cleaned with 75% ethanol after each trial.

Gene expression analysis by qRT-PCR

Pomc gene levels in the mediobasal hypothalamus (MBH) samples were measured by quantitative real-time polymerase chain reaction (RT-PCR) (SYBR Green assay) as described previously [26]. Total RNA was isolated from tissue samples using an RNeasy kit (Qiagen, Valencia, CA). Total RNA (1 μg) was converted to first-strand complementary DNA (cDNA) using a high-capacity cDNA reverse transcription kit (Life Technologies). The primer sequences used for Pomc, Gapdh, 18S, and Rpl19 are presented in Table 1. Real-time quantitative PCR was performed at 95°C for 5 minutes, followed by 40 cycles of 95°C for 15 seconds, 60°C for 30 seconds, and 72°C for 40 seconds in the Applied Biosystems 7500 real-time PCR system (Foster City, CA). The quantity of target genes (Pomc) and the three reference genes (Gapdh, 18S, and Rpl19) were measured using the standard curve method. Target-gene expression was normalized with reference gene expression levels.

[Figure omitted. See PDF.]

Table 1. Primer sequences.

https://doi.org/10.1371/journal.pone.0263340.t001

DNA methylation analysis by bisulfite pyrosequencing

In order to characterize the extent of cytosine methylation of CpG dinucleotides in the Pomc proximal promoter, we designed bisulfite sequencing primers in the CpG island. The methods for Pomc bisulfite pyrosequencing were as described previously [27]. A MethPrimer program was used to assess the CpG island and bisulfite sequencing primers for Pomc gene promoter (Table 1). Genomic DNA was extracted from MBH samples using DNeasy kit (Qiagen). About 1 ug of DNA was subjected to bisulfite treatment using EZ DNA methylation kit (Zymo Research, Orange, CA). Following bisulfite treatment, PCR reaction was performed with bisulfite sequencing primers using Pyromark PCR reagents (Qiagen, Valencia, CA) as detailed in the manufacturer’s protocols. Pyrosequencing was carried out using a sequencing primer on a PSQ-HS-96A model pyrosequencer (Qiagen). In the study, we analyzed one control C in a non-CpG background for efficient C→T conversion. This CpG site provides a built-in control for bisulfite treatment. Each CpG in the study was analyzed by comparing C/T peaks. The peak heights in the resulting pyrogram report the ratio of cytosine to thymine at each analyzed CpG site and reflects the portion of methylated DNA. The percentage of methylation was calculated and represented using the following formula:

% of methylation = percent C remaining as C in each target CpGX Control C → T %.

It is a highly sensitive method to detect and quantify small changes in methylation levels. The built-in control ensures the reliability of the results.

Statistical analysis

The data shown in the figures and text are mean ± SEM. Comparisons between groups were made using one-way analysis of variance (ANOVA) with post hoc analysis using the Newman Keuls posttest. Two-way ANOVA with Bonferroni post hoc tests were used for multiple comparisons. Significance was set at p<0.05. We used Prism 5.0 software for the analysis.

Results

Fetal alcohol exposure reduces Pomc gene expression in the mediobasal hypothalamus of male offspring rats for multiple generations

To determine the impact of fetal alcohol exposure in the inheritance of stress axis abnormalities, we first measured the changes in gene expression of a stress regulatory hormone Pomc in offspring during three generations. In the transgenerational study, we employed selected breeding procedures to determine if the transgenerational transmission of FAE effects is male or female germline specific. Determination of Pomc mRNA levels in the mediobasal hypothalamus (MBH) revealed that feeding an alcohol-containing liquid diet (AF), but not pair-feeding an isocaloric liquid diet (PF), significantly reduced the levels of Pomc gene expression in the MBH of F1 generation male and female offspring (Fig 1A and 1B). The suppressive effect of fetal alcohol on Pomc gene expression persisted in subsequent F2 and F3 generation offspring in a sex- and germline-dependent manner. We found the Pomc gene expression level was significantly lower in male offspring derived from the fetal alcohol-fed male germline (AFM) in the F2 and F3 generations (Fig 1C and 1E). However, the Pomc gene expression level did not change in male offspring derived from the fetal alcohol-fed female germline (AFF) or in female offspring derived from the alcohol-fed male germline (AFM) or female germline (AFF) in the F2 and F3 generations (Fig 1D and 1F). We also did not find any effect of pair-feeding the isocaloric liquid diet (PF) on Pomc gene expression in male or female offspring of any germline during F2 to F3 generation breeding (Fig 1). These data are in agreement with the previous finding that fetal alcohol exposure -induced changes in Pomc gene expression is transmitted to multiple generations via the male germline in Sprague Dawley rats [2].

[Figure omitted. See PDF.]

Fig 1. Transgenerational changes in Pomc mRNA levels in fetal alcohol exposed offspring for three generations.

Changes in the level of Pomc mRNA in the mediobasal hypothalamus of male and female offspring of pregnant rats fed an alcohol-containing liquid diet (AF), pair-fed an isocaloric liquid diet (PF), or ad lib-fed rat chow (AD) in the F1 generation (A, B), and in male and female offspring bred from the alcohol-fed male germline (AFM) or female germline (AFF) or pair-fed male germline (PFM) or female germline (PFF) in F2 (C, D) and F3 (E, F) generations. Data are mean ± SEM (n = 8 rats) and analyzed using one-way ANOVA followed by the Student Newman-Keuls post hoc test, and significant differences are indicated by ap<0.05, compared to AD; bp<0.05, compared to PF or PFF; cp<0.05, compared to PFM; dp<0.05, compared to the AFF group.

https://doi.org/10.1371/journal.pone.0263340.g001

Fetal alcohol exposure induces transgenerational effect on Pomc promoter DNA methylation in the mediobasal hypothalamus of male offspring rats for multiple generations

It is now well recognized that epigenetic modifications of a gene play an important role in the control of its transcription. Global or site-specific methylation of CpG sites near and within the regulatory regions of genes is often associated with transcriptional inactivity and gene suppression [28]. Therefore, we determined if the fetal alcohol exposure -induced changes in Pomc gene expression is associated with the altered promoter DNA methylation. Using the Methyl Primer Express v1.0 program (ABI, Waltham, MA), we previously identified three potential CpGs: CpG1 (-238), CpG2 (-224), and CpG3 (-216) in Pomc promoter CpG islands. We also showed FAE altered the methylation status of these CpGs by employing pyrosequencing, which is highly sensitive in determining methylation status at single CpG resolution [27]. Using the pyrosequencing methods, we show here FAE alters Pomc gene methylation at various CpG sites of Pomc promoter CpG islands in a sex- and germline-dependent manner (Fig 2). FAE increased methylation levels of all three different CpGs across Pomc promoter CpG islands in the MBH of both male and female F1 offspring (Fig 2A and 2B). In F2 and F3 generation males, Pomc promoter methylation levels of CpG1 (-238) and CpG3 (-216) were significantly increased only in offspring of the male germline (AFM) but not in the female germline (AFF) (Fig 2C and 2E). In F2 and F3 generation females, Pomc promoter methylation levels did not change in offspring of AFM and AFF germlines (Fig 2D and 2F). This method of bisulfite pyrosequencing is a highly sensitive one to detect even small changes in DNA methylation of each CpG. We previously measured changes in DNA methylation of these three potential CpGs of POMC promoter and its correlation with expression (2, 26). Although the increased changes in DNA methylation of these CpGs are small, they are correlated with reduced expression of POMC as we reported previously. These data are in agreement with our previous findings that fetal alcohol exposure increased Pomc gene methylation is transmitted to multiple generations via the male germline in outbred Sprague Dawley rats [2]. Therefore, the male-germline-specific transgenerational effects of FAE on Pomc gene transcription is related to epigenetic modifications of the gene promoter and not to genetic variations of the animals.

[Figure omitted. See PDF.]

Fig 2. Transgenerational changes in Pomc DNA methylation levels in fetal alcohol exposed offspring for three generations.

Transgenerational changes in Pomc DNA promoter methylation in male and female AF, PF, or AD offspring in the F1 generation (A, B), and in AFM, AFF, PFM, and PFF in F2 (C, D) and F3 (E, F) generations. Pomc gene methylation at various CpG sites of Pomc promoter CpG islands CpG1 (-238), CpG2 (-224), and CpG3 (-216) were measured using pyrosequencing. Data are mean ± SEM (n = 9 rats) and analyzed using one-way ANOVA followed by the Student Newman-Keuls post hoc test. Significant differences are indicated by ap<0.05, compared to AD; bp<0.05, compared to PF or PFF; cp<0.05, compared to PFM; dp<0.05, compared to the AFF group.

https://doi.org/10.1371/journal.pone.0263340.g002

Transgenerational effects of fetal alcohol exposure on corticosterone response to a restraint stress challenge

To evaluate whether the transgenerational effect of fetal alcohol exposure applies to some endophenotypes of the Pomc defect, we determined stress hormone response to restraint stress in F1–F3 rat offspring. It was observed that fetal alcohol exposure increased plasma levels of corticosterone in response to 60 minutes of restraint stress, which persisted 60 minutes following restraint in both male and female offspring of F1 progeny (Fig 3A and 3C). The total amount of corticosterone released during the 120-minute period, as determined by the area under the curve, was also increased in both sexes in this generation’s progeny (Fig 3B and 3D). In the F2 male progeny, the corticosterone response to restraint stress was significantly elevated in both AFM and AFF germlines as determined by time response (Fig 3E and 3G) and the area under the curve (Fig 3F). In the F2 female progeny, the corticosterone response to stress fluctuated and showed a moderate reduction in the control-fed male germline (PFM), as well as in AFF and AFM groups (Fig 3G and 3H). In the F3 male progeny, the corticosterone response to restraint stress was significantly elevated in AFM but not in the AFF germline as determined by time response (Fig 3I) and the area under the curve (Fig 3J). No changes of corticosterone response to restraint were found in F3 female progeny in AFF or AFM germlines (Fig 3K and 3L). These results suggest that fetal alcohol’s effects on stress axis abnormalities perpetuate into subsequent generations through the male germline.

[Figure omitted. See PDF.]

Fig 3. Transgenerational changes in plasma corticosterone response to restraint stress in fetal alcohol exposed offspring.

Corticosterone responses to restraint stress were evaluated in male and female rat offspring (on day of diestrus) at day 60 after birth from male and female e germlines. Time-dependent changes of cortisol before, during, and after restraint are shown for each group for F1 males and females (A, C), F2 males and females (E, G), and F3 males and females (I, K). Data are mean ± SEM (n = 8 rats) and analyzed using two-way ANOVA followed by Tukey’s multiple comparison post hoc test. Significant differences of the hormone response at the same time point between groups are indicated by ap<0.05, compared to AD; bp<0.05, compared to PF or PFF; cp<0.05, compared to PFM; dp<0.05, and compared to the AFF group. Total levels of corticosterone released during the restraint stress study as determined by the area under curve for F1 (B, D), F2 (F, H), and F3 (J, L) male and female offspring from different germlines (n = 8 rats). Data are mean ± SEM (n = 8 rats) and analyzed using one-way ANOVA followed by the Student Newman-Keuls post hoc test. ap<0.05, compared to AD; bp<0.05, compared to PF or PFF; dp<0.05, and compared to the AFF group.

https://doi.org/10.1371/journal.pone.0263340.g003

Transgenerational effects of fetal alcohol exposure on anxiety-like behaviors

We also tested the effects of fetal alcohol exposure on anxiety-like behavior. The Elevated Plus Maze data showed that fetal alcohol exposure induced a significant increase in the amount of time spent in closed arms and a significant decrease in time spent in open arms in the AF group when compared to AD and PF groups in both the male and female F1 offspring (Fig 4A–4D). In the F2 generation, the male offspring of the male germline (AFM) also showed a significant increase in the amount of time spent in closed arms and a significant decrease in time spent in open arms as compared to controls, whereas the female germline (AFF) did not show any significant change in time spent in closed and open arms as compared to controls in both male and female rats (Fig 4E–4H). In the F3 generation, the male and female progeny of the male germline (AFM) also showed a significant increase in the amount of time spent in closed arms as compared to controls (Fig 4I–4L). However, the F3 male and female progeny of the female germline (AFF) did not show any change. Also, no significant changes were observed in the amount of time spent in open arms in F3 generation male and female progeny (Fig 4I–4L).

[Figure omitted. See PDF.]

Fig 4. Transgenerational changes on anxiety-like behaviors in fetal alcohol exposed offspring.

Effect of prenatal ethanol exposure on anxiety-like behaviors as determined by the elevated plus maze (EPM) in male and female offspring of F1, F2, and F3 generations. For EPM analysis, time (sec) in closed and open arms was analyzed in F1-F3 generation rats. Data are expressed as mean ± SEM, n = 8 in each condition. The data were analyzed using one-way ANOVA followed by the Student Newman-Keuls post hoc test and significant differences are indicated by ap<0.05, compared to AD; bp<0.05, compared to PF or PFF; cp<0.05, compared to PFM; dp<0.05, compared to the AFF group.

https://doi.org/10.1371/journal.pone.0263340.g004

Discussion

Our previous studies in outbred Sprague Dawley rats suggest that the fetal alcohol exposure -induced methylation state of the Pomc gene and its endophenotypes is inherited through the male germline. Epigenetic states can be influenced by an underlying DNA sequence or be purely epigenetic (sequence-independent) [23]. We therefore assess the induction of heritable epigenetic Pomc-related variants by fetal alcohol exposure in isogenic F344 rats maintained in standardized conditions in order to control both genetic and environmental sources of variations. The data of this study indicate that in F344 rats, the F1, F2, and F3 male progeny of the AF mother’s male lineage had a significant increase in methylation levels in the proximal part of the Pomc promoter with the concomitant reduction in the Pomc mRNA level. DNA methylation or expression levels of Pomc did not change in F1, F2, or F3 male progeny of the PF mother’s male lineage as compared to controls. These data provide support to the view that FAE-induced epigenetic marks on the Pomc gene are heritable.

We showed here that fetal alcohol exposure induces long-lasting hypermethylation of the Pomc gene, since the percentage of the cytosine methylation of CpG sites adjacent to the gene transcription start site for Pomc was higher in FAE animals than in controls. Methylation of the proximal region of the promoter is known to correlate closely with a negative effect on gene expression [24]. Moreover, deletions or mutations in these promoter regions cause a decrease in gene expression for Pomc [29, 30]. Hence, increased DNA methylation in the key epigenetic island in the promoter regions of the Pomc gene could have reduced expression levels of this gene in the hypothalamus, which has been demonstrated in the fetal alcohol exposed offspring. In this context, it should be emphasized that administration of 5-azadeoxycytidine (AZA), a blocker of DNA methylation, DNA methyltransferases, prevents FAE-induced alteration of POMC gene expression and further transmission to the next generation via the offspring [2]. Overall, these findings provide evidence that FAE effects on Pomc hypermethylation and stress axis abnormalities persisted throughout adulthood and perpetuated into subsequent generations through the male germline [2].

The transgenerational effect of fetal alcohol exposure was also noted in some endophenotypes of the Pomc defect. We found an increase in the restraint stress-induced increase in corticosterone levels in male offspring of the F1, F2, and F3 progeny of the male germline. These male germline-dependent corticosterone responses to stress were like those of POMC gene methylation changes in F1 to F3 FAE offspring. Additionally, previous studies have shown that POMC neuronal transplants prevent a FAE-induced increase in corticosterone response to stress [31]. Therefore, FAE-induced epigenetic modification of the Pomc gene may also contribute, at least partly, to the multigenerational defects of the stress response in FAE offspring.

Behavioral testing across three generations also indicated that fetal alcohol exposure generates stable transgenerational increases in anxiety-like behaviors, persisting via the male germline to unexposed offspring. In our study, fetal alcohol exposure increased anxiety-like behaviors in the elevated plus maze because the FAE offspring showed an increased amount of time spent in the closed arm. These behavioral changes persisted in only male germline-derived male and female offspring for three generations. We also found a significant decrease in the amount of time spent in the open arms in both male and female offspring of the male germline for two generations and a moderate decrease (did not reach significant differences) in the third generation male and female progeny of the male germline. Previously it has been shown that transplantation of POMC neurons in the FAE offspring increased the number of entries into the open arms and reduced the time spent in closed arms relative to the control animals in an elevated plus maze [32], suggesting that POMC neurons contribute to the control of the anxiety-like behaviors in response to novel environments in fetal alcohol exposed animals. Thus, fetal alcohol exposure -induced POMC deficiency contributes at least partly to the increased anxiety-like behaviors in FAE offspring of the male germline for multiple generations. It should be noted that the transgenerational effect of fetal alcohol exposure on anxiety-like behavior is expressed in both male and female offspring of the male germline, while the transgenerational effect of fetal alcohol exposure on POMC gene methylation and expression are observed only in the male progeny of the male germline. Hence, there may be other undetermined factors which also contribute to the changes of these behaviors in female FAE offspring for male germline-dependent transgenerational transmission.

Epigenetic transgenerational inheritance was reported in a number of animal studies using exposure to environmental toxicants, diet restrictions, hormonal imbalance, and stress factors. Environmental exposure to vinclozoline, an endocrine disruptor, increases stress and anxiety in the F3 generation [33]. A maternal high-fat diet increases susceptibility of male offspring to liver disease through epigenetic reprogramming of lipid metabolism and inflammatory responses [34]. Postnatal trauma elicits depressive-like behavior for up to three generations [35]. A study has provided evidence for the implication of sperm microRNAs in transgenerational inheritance of trauma-induced phenotypes across generations [36]. Fetal alcohol exposure elicits epigenetic marks on interferon-γ that pass through multiple generations via the male germ line, providing evidence of FAE’s adverse effect on the immune system [37]. Some human studies provided evidence for epigenetic transgenerational inheritance. Transgenerational transmission of trauma has been studied in the offspring of veterans and refugee families [38, 39]. Studies have shown that a grandparent with a major depressive disorder with alcohol abuse increased the risk of an individual having major depressive behavior [40].

In conclusion, our data suggest that FAE induces heritable changes in POMC gene expression and affects the stress response and anxiety-like behaviors via epigenetic modifications for multiple generations via the male germline.

Supporting information

S1 Table. Power analysis of the POMC expression and methylation data to calculate sample size.

10.1371/journal.pone.0263340.s001

(DOCX)

Acknowledgments

We thank Stacey Pontoriero for editorial assistance and Miguel Cabrera for assistance in alcohol-feeding animals.

Citation: Gangisetty O, Chaudhary S, Palagani A, Sarkar DK (2022) Transgenerational inheritance of fetal alcohol effects on proopiomelanocortin gene expression and methylation, cortisol response to stress, and anxiety-like behaviors in offspring for three generations in rats: Evidence for male germline transmission. PLoS ONE 17(2): e0263340. https://doi.org/10.1371/journal.pone.0263340

References

1. Anway MD, Cupp AS, Uzumcu M, Skinner MK. Epigenetic transgenerational actions of endocrine disruptors and male fertility. Science 2005;308: 1466–1469. pmid:15933200

2. Govorko D, Bekdash RA, Zhang C, Sarkar DK. Male germline transmits fetal alcohol adverse effect on hypothalamic proopiomelanocortin gene across generations. Biol Psychiatry 2012;72: 378–388. pmid:22622000

3. Nizhnikov ME, Popoola DO, Cameron NM. Transgenerational transmission of the effect of gestational ethanol exposure on ethanol use-related behavior. Alcohol Clin Exp Res. 2016;40: 497–506. pmid:26876534

4. Finegersh A, Rompala GR, Martin DI, Homanics GE. Drinking beyond a lifetime: New and emerging insights into paternal alcohol exposure on subsequent generations. Alcohol 2015;49: 461–470. pmid:25887183

5. Yohn NL, Bartolomei MS, Blendy JA. Multigenerational and transgenerational inheritance of drug exposure: the effects of alcohol, opiates, cocaine, marijuana, and nicotine. Prog Biophys Mol Biol. 2015;118: 21–33. pmid:25839742

6. Minguez L, Ballandonne C, Rakotomalala C, Dubreule C, Kientz-Bouchart V, Halm-Lemeille MP. Transgenerational effects of two antidepressants (sertraline and venlafaxine) on Daphnia magna life history traits. Environ Sci Technol. 2015;49: 1148–1155. pmid:25506746

7. VandeVoort CA, Grimsrud KN, Midic U, Mtango N, Latham KE. Transgenerational effects of binge drinking in a primate model: implications for human health. Fertil Steril. 2015;103: 560–569. pmid:25492684

8. Vassoler FM, Byrnes EM, Pierce RC. The impact of exposure to addictive drugs on future generations: physiological and behavioral effects. Neuropharmacology 2014;76(Pt B): 269–275. pmid:23810828

9. Babenko O, Kovalchuk I, Metz GA. Stress-induced perinatal and transgenerational epigenetic programming of brain development and mental health. Neurosci Biobehav Rev. 2015;48: 70–91. pmid:25464029

10. Dunn GA, Bale T. Maternal high-fat diet effects on third-generation female body size via the paternal lineage. Endocrinology 2011;152: 2228–2236. pmid:21447631

11. Zuo L, Wang K, Zhang X, Pan X, Wang G, Krystal JH, et al. Sex chromosome-wide association analysis suggested male-specific risk genes for alcohol dependence. Psychiatr Genet. 2013;23: 233–238. pmid:23907288

12. Manzardo AM, Henkhaus R, Hidaka B, Penick EC, Poje AB, Butler MG. X chromosome inactivation in women with alcoholism. Alcohol Clin Exp Res. 2012;36: 1325–1329. pmid:22375556

13. Liu XQ, Greenwood CM, Wang KS, Paterson AD. A genome scan for parent-of-origin linkage effects in alcoholism. BMC Genet. 2005;30(6 Suppl 1):S160. pmid:16451622

14. Lemire M. A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage. BMC Genet. 2006;30(6 Suppl 1):S159. pmid:16451620

15. Bruner-Tran KL, Gnecco J, Ding T, Glore DR, Pensabene V, Osteen KG. Exposure to the environmental endocrine disruptor TCDD and human reproductive dysfunction: translating lessons from murine models. Reprod Toxicol. 2016 Mar. pii: S0890-6238(16)30264-7. pmid:27423904

16. Miller LL, Pembrey M, Davey Smith G, Northstone K, Golding J. Is the growth of the fetus of a non- smoking mother influenced by the smoking of either grandmother while pregnant? PLoS One. 2014;9:e86781. pmid:24504157

17. Little RE, Sing CF. Father’s drinking and infant birth weight: report of an association. Teratology 1987;36: 59–65. pmid:3672378

18. Abel EL. Paternal contribution to fetal alcohol syndrome. Addiction Biology 2001;9: 127–133. pmid:15223537

19. Hegedus AM, Alterman AI, Tarter RE. Learning achievement in sons of alcoholics. Alcohol Clin Exp Res. 1984;8: 330–33. pmid:6377954

20. Tarter RE, Hegedus AM, Goldstein S, Shelly C, Alterman AI. Adolescent sons of alcoholics: neuropsychological and personality characteristics. Alcohol Clin Exp Res. 1984;8: 216–222. pmid:6375434

21. Ouko LA, Shantikumar K, Knezovich J, Haycock P, Schnugh DJ, Ramsay M. Effect of alcohol consumption on CpG methylation in the differentially methylated regions of H19 and IG-DMR in male gametes: implications for fetal alcohol spectrum disorders. Alcohol Clin Exp Res. 2009;33: 1615–1627. pmid:19519716

22. Sarkar DK, Gangisetty O, Wozniak JR, Eckerle JK, Georgieff MK, Foroud TM, et al. Persistent changes in stress-regulatory genes in pregnant women or children exposed prenatally to alcohol. Alcohol Clin Exp Res. 2019;43: 1887–1897. pmid:31329297

23. Richards EJ. Inherited epigenetic variation—revisiting soft inheritance. Nat Rev Genet. 2006;7: 395–401. pmid:16534512

24. Miller MW, Circadian rhythm of cell proliferation in the telencephalic ventricular zone: effect of in utero exposure to ethanol. Brain Res. 1992;595: 17–24. pmid:1467954

25. Jawhar S, Trawicka A, Jenneckens C, Bayer TA, Wirths O. Motor deficits, neuron loss, and reduced anxiety coinciding with axonal degeneration and intraneuronal Aβ aggregation in the 5XFAD mouse model of Alzheimer’s disease. Neurobiol Aging. 2012;33:196.e29–40. pmid:20619937

26. Gangisetty O, Bekdash R, Maglakelidze G, Sarkar DK. Fetal alcohol exposure alters proopiomelanocortin gene expression and hypothalamic-pituitary-adrenal axis function via increasing MeCP2 expression in the hypothalamus. PLoS One. 2014;9: e113228. pmid:25409090

27. Jabbar S, Chastain LG, Gangisetty O, Cabrera MA, Sochacki K, Sarkar DK. Preconception alcohol increases offspring vulnerability to stress. Neuropsychopharmacology 2016;41: 2782–2793. pmid:27296153

28. MacDonald JL, Roskams AJ. Epigenetic regulation of nervous system development by DNA methylation and histone deacetylation. Prog Neurobiol. 2009;88: 170–183. pmid:19554713

29. Sotnikov SV, Markt PO, Malik V, Chekmareva NY, Naik RR, Sah A, et al. Bidirectional rescue of extreme genetic predispositions to anxiety: impact of CRH receptor 1 as epigenetic plasticity gene in the amygdala. Transl Psychiatry 2014;11: e359. pmid:24518397

30. Ehrlich S, Weiss D, Burghardt R, Infante-Duarte C, Brockhaus S, Muschler MA, et al. Promoter specific DNA methylation and gene expression of POMC in acutely underweight and recovered patients with anorexia nervosa. J Psychiatr Res 2010;44: 827–833. pmid:20176366

31. Boyadjieva NI, Ortigüela M, Arjona A, Cheng X, Sarkar DK. Beta-endorphin neuronal cell transplant reduces corticotropin releasing hormone hyperresponse to lipopolysaccharide and eliminates natural killer cell functional deficiencies in fetal alcohol exposed rats. Alcohol Clin Exp Res. 2009;33: 931–937. pmid:19320628

32. Logan RW, Wynne O, Maglakelidze G, Zhang C, O’Connell S, Boyadjieva NI, et al. β-endorphin neuronal transplantation into the hypothalamus alters anxiety-like behaviors in prenatal alcohol-exposed rats and alcohol-non-preferring and alcohol-preferring rats. Alcohol Clin Exp Res. 2015;39: 146–57. pmid:25623413

33. Crews D, Gillette R, Scarpino SV, Manikkam M, Savenkova MI, Skinner MK. Epigenetic transgenerational inheritance of altered stress responses. Proc Natl Acad Sci U S A. 2012;109: 9143–9148. pmid:22615374

34. Pruis MGM, Lendvai A, Bloks VW, Zwier MV, Baller JFW, de Bruin A, et al. Maternal western diet primes non-alcoholic fatty liver disease in adult mouse offspring. Acta Physiol. 2014;210: 215–227. pmid:24224789

35. Franklin TB, Russig H, Weiss IC, Gräff J, Linder N, Michalon A, et al. Epigenetic transmission of the impact of early stress across generations Biol Psychiatry 2010;68: 408–415. pmid:20673872

36. Gapp K, Jawaid A, Sarkies P, Bohacek J, Pelczar P, Prados J, et al. Implication of sperm RNAs in transgenerational inheritance of the effects of early trauma in mice. Nat Neurosci. 2014;17:667–669. pmid:24728267

37. Gangisetty O, Palagani A, Sarkar DK. Transgenerational inheritance of fetal alcohol exposure adverse effects on immune gene interferon-ϒ. Clin Epigenetics. 2020;;12:70. pmid:32448218; PMCID: PMC7245772.

38. Vaage AB, Thomsen PH, Rousseau C, Wentzel-Larsen T, Ta TV, Hauff E. Paternal predictors of the mental health of children of Vietnamese refugees. Child Adolesc Psychiatry Ment Health 2011;5:2. pmid:21219651

39. Kellermann NP. Epigenetic transmission of holocaust trauma: can nightmares be inherited? Isr J Psychiatry Relat Sci. 2013;50: 33–39. pmid:24029109

40. Olino TM, Pettit JW, Klein DN, Allen NB, Seeley JR, Lewinsohn PM. Influence of parental and grandparental major depressive disorder on behavior problems in early childhood: a three-generation study. J Am.Acad.Child Adolesc Psychiatry 2008;47: 53–60. pmid:18174825