1. Developmental Biology
  2. Genetics and Genomics

Early moderate prenatal alcohol exposure and maternal diet impact offspring DNA methylation across species

  1. Mitchell Bestry
  2. Alexander N Larcombe
  3. Nina Kresoje
  4. Emily K Chivers
  5. Chloe Bakker
  6. James P Fitzpatrick
  7. Elizabeth J Elliott
  8. Jeffrey M Craig
  9. Evelyne Muggli
  10. Jane Halliday
  11. Delyse Hutchinson
  12. Sam Buckberry
  13. Ryan Lister
  14. Martyn Symons
  15. David Martino  Is a corresponding author
  1. Telethon Kids Institute, The University of Western Australia, Australia
  2. Respiratory Environmental Health, Wal-yan Respiratory Research Centre, Telethon Kids Institute, Australia
  3. Occupation, Environment and Safety, School of Population Health, Curtin University, Australia
  4. Telethon Kids Institute, Australia
  5. School of Psychological Sciences, University of Western Australia, Australia
  6. University of Sydney, Faculty of Medicine and Health, Specialty of Child and Adolescent Health, Australia
  7. Sydney Children’s Hospitals Network (Westmead) and Kids Research, Australia
  8. Deakin University, IMPACT – the Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Australia
  9. Murdoch Children’s Research Institute, Royal Children’s Hospital, Australia
  10. Department of Paediatrics, University of Melbourne, Royal Children’s Hospital, Australia
  11. Reproductive Epidemiology, Murdoch Children's Research Institute, Australia
  12. Deakin University, School of Psychology, Faculty of Health, Australia
  13. Murdoch Children’s Research Institute, Centre for Adolescent Health, Royal Children’s Hospital, Australia
  14. University New South Wales, National Drug and Alcohol Research Centre, Australia
  15. Harry Perkins Institute of Medical Research, QEII Medical Centre and Centre for Medical Research, The University of Western Australia, Australia
  16. ARC Centre of Excellence in Plant Energy Biology, School of Molecular Sciences, The University of Western Australia, Australia
  17. National Drug Research Institute, enAble Institute, Curtin University, Australia
  18. Wal-yan Respiratory Research Centre, Telethon Kids Institute, Australia
https://doi.org/10.7554/eLife.92135.3
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Cite this article
  1. Mitchell Bestry
  2. Alexander N Larcombe
  3. Nina Kresoje
  4. Emily K Chivers
  5. Chloe Bakker
  6. James P Fitzpatrick
  7. Elizabeth J Elliott
  8. Jeffrey M Craig
  9. Evelyne Muggli
  10. Jane Halliday
  11. Delyse Hutchinson
  12. Sam Buckberry
  13. Ryan Lister
  14. Martyn Symons
  15. David Martino
(2024)
Early moderate prenatal alcohol exposure and maternal diet impact offspring DNA methylation across species
eLife 12:RP92135.
https://doi.org/10.7554/eLife.92135.3
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eLife assessment

This important study unveils the significant impact of prenatal alcohol exposure on epigenetic patterns, offering new insights into its adverse health outcomes through solid evidence from both mouse models and human data. The findings, which reveal how a high-methyl diet can mitigate these epigenetic alterations, present a promising prenatal care strategy. Despite its solid data overall, the study's small sample size and unaccounted confounders suggest the need for further research to confirm these findings and explore their practical implications.

https://doi.org/10.7554/eLife.92135.3.sa0

Abstract

Alcohol consumption in pregnancy can affect genome regulation in the developing offspring but results have been contradictory. We employed a physiologically relevant murine model of short-term moderate prenatal alcohol exposure (PAE) resembling common patterns of alcohol consumption in pregnancy in humans. Early moderate PAE was sufficient to affect site-specific DNA methylation in newborn pups without altering behavioural outcomes in adult littermates. Whole-genome bisulfite sequencing of neonatal brain and liver revealed stochastic influence on DNA methylation that was mostly tissue-specific, with some perturbations likely originating as early as gastrulation. DNA methylation differences were enriched in non-coding genomic regions with regulatory potential indicative of broad effects of alcohol on genome regulation. Replication studies in human cohorts with fetal alcohol spectrum disorder suggested some effects were metastable at genes linked to disease-relevant traits including facial morphology, intelligence, educational attainment, autism, and schizophrenia. In our murine model, a maternal diet high in folate and choline protected against some of the damaging effects of early moderate PAE on DNA methylation. Our studies demonstrate that early moderate exposure is sufficient to affect fetal genome regulation even in the absence of overt phenotypic changes and highlight a role for preventative maternal dietary interventions.

eLife digest

Drinking excessive amounts of alcohol during pregnancy can cause foetal alcohol spectrum disorder and other conditions in children that affect their physical and mental development. Many countries advise women who are pregnant or trying to conceive to avoid drinking alcohol entirely. However, surveys of large groups of women in Western countries indicate that most women continue drinking low to moderate amounts of alcohol until they discover they are pregnant and then stop consuming alcohol for the rest of their pregnancy. It remains unclear how this common drinking pattern affects the foetus.

The instructions needed to build and maintain a human body are stored within molecules of DNA. Some regions of DNA called genes contain the instructions to make proteins, which perform many tasks in the body. Other so-called ‘non-coding’ regions do not code for any proteins but instead have roles in regulating gene activity. One way cells control which genes are switched on or off is adding or removing tags known as methyl groups to certain locations on DNA. Previous studies indicate that alcohol may affect how children develop by changing the patterns of methyl tags on DNA.

To investigate the effect of moderate drinking during the early stages of pregnancy, Bestry et al. exposed pregnant mice to alcohol and examined how this affected the patterns of methyl tags on DNA in their offspring. The experiments found moderate levels of alcohol were sufficient to alter the patterns of methyl tags in the brains and livers of the newborn mice. Most of the changes were observed in non-coding regions of DNA, suggesting alcohol may affect how large groups of genes are regulated. Fewer changes in the patterns of methyl tags were found in mice whose mothers had diets rich in two essential nutrients known as folate and choline.

Further experiments found that some of the affected mouse genes were similar to genes linked to foetal alcohol spectrum disorder and other related conditions in humans. These findings highlight the potential risks of consuming even moderate levels of alcohol during pregnancy and suggest that a maternal diet rich in folate and choline may help mitigate some of the harmful effects on the developing foetus.

Introduction

Alcohol consumption in pregnancy is a leading cause of neurodevelopmental impairments in children (Popova et al., 2023). Alcohol can pass through the placenta acting as a teratogen in fetal tissues causing physical, cognitive, behavioural, and neurodevelopmental impairment in children at high doses with lifelong consequences for health (Chung et al., 2021). Fetal alcohol spectrum disorder (FASD) and fetal alcohol syndrome (FAS) can arise at binge levels of exposure, although not always at lower levels of exposure. Whether prenatal alcohol exposure (PAE) is sufficient to induce overt physiological abnormalities depends on multiple environmental and genetic factors including the dose and timing of alcohol use during pregnancy, maternal diet, smoking, stress, and potentially other factors that collectively influence fetal outcomes (Chung et al., 2021; Jacobson et al., 2021; Sambo and Goldman, 2023).

Patterns of alcohol consumption in pregnancy vary, but epidemiological surveys suggest most women in Western countries consume low to moderate levels between conception until recognition of pregnancy (Tsang et al., 2022), after which time consumption largely ceases, apart from occasional use (McCormack et al., 2017). While the effects of binge levels of exposure are well documented as able to cause FASD, more subtle effects that reflect the more common patterns of drinking are unclear and more research is needed to support public health initiatives to reduce alcohol consumption in pregnancy.

Studies suggest alcohol can disrupt fetal gene regulation through epigenetic mechanisms (Bestry et al., 2022). DNA methylation is one epigenetic mechanism involving the catalytic addition of methyl groups to cytosine bases within cytosine-guanine (CpG) dinucleotide motifs during one-carbon metabolism. Methylation of DNA can alter chromatin density and influence patterns of gene expression in a tissue-specific and developmentally appropriate manner and disruption to this process may cause some of the difficulties experienced by people with FASD (Jin and Liu, 2018; Fransquet et al., 2016). Previous studies on human participants (Lussier et al., 2018; Masemola et al., 2015; Jarmasz et al., 2019; Portales-Casamar et al., 2016) and animals (Chen et al., 2013; Abbott et al., 2018; Downing et al., 2011) report that alcohol can disrupt DNA methylation either globally (Jarmasz et al., 2019; Portales-Casamar et al., 2016; Chen et al., 2013; Abbott et al., 2018) or at specific gene regions (Masemola et al., 2015; Abbott et al., 2018; Downing et al., 2011). Our recent systematic review, however, found limited replication of effects between studies suggesting the effects of alcohol on DNA methylation may be stochastic and influenced by numerous confounding factors (Bestry et al., 2022). PAE can either directly inhibit DNA methyltransferase enzymes or disrupt one-carbon metabolism via inhibition of bioavailability of dietary methyl donors, such as folate and choline to the fetus (Chen et al., 2011; Hutson et al., 2012). Choline, in particular, has been explored in several clinical trials to reduce cognitive deficits caused by PAE in affected individuals (Nguyen et al., 2016; Wozniak et al., 2020), or when administered during pregnancy (Jacobson et al., 2018; Thomas et al., 2009), with results suggesting a high methyl donor (HMD) diet could at least partially mitigate the adverse effects of PAE on various behavioural outcomes.

Given the lack of clarity around the effects of typical patterns of alcohol consumption, which often do not cause observable phenotypes, we conducted an epigenome-wide association study of early moderate PAE in mice. Regions identified as sensitive to gestational alcohol exposure were replicated in human cohorts. The study was a controlled intervention investigating the impact of early moderate PAE on offspring DNA methylation comparing exposed and unexposed mice, with an additional arm comparing the effect of alcohol exposure in the context of an HMD maternal diet. The exposure period covers the equivalent of pre-conception up until the first trimester in humans when neurulation occurs, reflecting a typical situation in which women may consume alcohol up until pregnancy recognition (Tsang et al., 2022; Muggli et al., 2016). The primary outcome of the study was differences in offspring DNA methylation and secondary outcomes of behavioural deficits across neurodevelopmental domains relevant to FASD were also examined. We employed whole-genome bisulfite sequencing (WGBS) for unbiased assessment of CpG DNA methylation in newborn brain and liver, two target organs affected by ethanol (Zakhari, 2006), to explore tissue specificity of effects and to determine any ‘tissue agnostic’ effects which may have arisen prior to the germ layers separating in early gastrulation. We also conducted candidate gene testing of regions identified in prior studies as sensitive to early moderate PAE. Our study provides cogent evidence that common patterns of drinking can have measurable effects on fetal gene regulation, highlighting a role for maternal dietary support in public health interventions.

Results

Comparison of prenatal characteristics across treatment groups

To investigate the effects of early moderate PAE and an HMD diet across pregnancy on offspring DNA methylation and behavioural outcomes, we employed a murine model with four treatment groups. Treatment groups were designed to assess the effect of alcohol on offspring DNA methylation compared to control mice. An additional treatment group included a maternal diet high in methyl donors, with and without alcohol exposure (Figure 1).

Figure 1
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Overview of prenatal alcohol exposure (PAE) model.

A schematic representation of the experiment design is shown in the figure. Fifteen dams were allocated to each treatment group. PAE mice were exposed to ethanol (10% vol/vol in non-acidified reverse osmosis drinking water ad libitum) from 1 week before pregnancy to gestational days 8–10 and the remaining mice received water (H2O). The PAE and H2O groups received either normal chow (NC) or a high methyl donor (HMD) diet (NC containing 20 mg/kg folate and 4970 mg/kg choline) from 1 week before pregnancy until birth.

The trajectory of weight gain during pregnancy was similar across all treatment groups with some evidence of more rapid weight gain in the HMD groups in the last 2 days (linear mixed effects regression model; H2O-HMD: –2.282±0.918 g, p=0.0177; PAE-HMD: –1.656±0.814 g, p=0.0493; Figure 2a), although the total amount of weight gained between days 1 and 17–19 was not significantly different between treatment groups by linear mixed effects regression (Figure 2a and b). The total amount of liquid consumed over the course of pregnancy was significantly lower in HMD dams by unpaired t-test (Figure 2b and Figure 3c). There was no significant difference in the average litter size (6.525±0.297 pups, Figure 2c) and pup sex ratios (Figure 2d) between treatment groups by unpaired t-test.

Figure 2
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PAE and HMD effects on dam characteristics.

(a) Dam weight progression was significantly affected by HMD but not PAE by quadratic mixed effects model without interaction. (b) Trajectory of liquid consumption across pregnancy was affected by PAE and HMD by quadratic mixed effects model. PAE and HMD significantly interacted with trimester of pregnancy. (c) Litter size (N=40) and (d) pup sex ratios (N=36) were not significantly associated with PAE or HMD by unpaired t-test or ANOVA. All line and bar plots show mean and standard deviation. NC = normal chow, HMD = high methyl diet, PAE = prenatal alcohol exposure. Comparisons show p-value by unpaired t-test compared to the H2O-NC baseline treatment group.

Figure 3
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Prenatal alcohol exposure (PAE) and high methyl donor (HMD) effects on dam characteristics.

There was no significant difference in the average gain of weight in dams between (a) days 1–17 and (b) days 1–19 by treatment group. Both timepoints were included due to some pregnancies ending by day 19. (c) Dams given supplemented chow consumed significantly lower total quantity of liquid across pregnancy. Bar plots show mean and standard deviation for each treatment group. Each point represents one dam. (d) The trajectory of chow consumed by dams across pregnancy significantly varied with the addition of treatments. Points show mean and standard deviation for each treatment group. Statistical analysis involved linear mixed effects regression comparing trajectories of treatment groups to H2O-NC baseline control group. N=36.

Effects of early moderate PAE on DNA methylation in newborn mice tissue

A subset of 16 newborn pups (n=4 per treatment) matched for sex and litter size were selected for WGBS. Both neonatal brain and liver were harvested to investigate the effects of early moderate PAE on fetal CpG DNA methylation. A total of 21,842,961 CpG sites were initially available for analysis.

Global levels of DNA methylation stratified across different genomic contexts were preserved across treatment conditions, with no major differences in average DNA methylation content between groups (Figure 4). To investigate region-specific effects of early moderate PAE on newborn DNA methylation, we conducted genome-wide testing comparing exposed and unexposed mice on the normal chow. We identified 78 differentially methylated regions (DMRs) in the brain and 759 DMRs in the liver (p<0.05 and mean difference in methylation across the DMR with PAE (delta) >0.05) from ~19,000,000 CpG sites tested after coverage filtering (Figure 5a and b). These regions were annotated to nearby genes using annotatr and are provided in Supplementary file 1a and b. Two of the DMRs overlapped in mouse brain and liver (tissue agnostic), but the remainder were tissue specific. Among these tissue agnostic regions was the Impact gene on chromosome 18, which had lower methylation in PAE+NC mice compared to H2O+NC mice in both the brain and liver (Figure 5c and d). The other tissue agnostic region was within 5 kb downstream of Bmf and had higher DNA methylation in brain and liver tissue of PAE+NC mice.

Figure 4
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No evidence for global disruption of methylation by prenatal alcohol exposure (PAE).

The figure shows methylation levels averaged across cytosine-guanines (CpGs) in different regulatory genomic contexts. Neither brain tissue (a and b) nor liver tissue (c and d) were grossly affected by PAE exposure (blue bars). Bars represent means and standard deviation.

Figure 5
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Prenatal alcohol exposure (PAE) was associated with site-specific differences in offspring DNA methylation.

The majority of differentially methylated regions (DMRs) lost methylation with PAE in (a) brain and (b) liver of mice given normal chow (NC). Each point represents one DMR. Point colour indicates change in DNA methylation with PAE. PAE was also associated with lower methylation in the DMRs identified in the promoter of the Impact gene in (c) brain and (d) liver, within NC mice. Each plot represents a separate treatment group. Each blue vertical line indicates a cytosine-guanine (CpG) site, with the height and corresponding left y-axis indicating the methylation ratio. The grey line and corresponding right y-axis indicate coverage at each CpG site. The black horizontal dotted line indicates 40% methylation for comparison purposes. The x-axis indicates the base position on chromosome 18, with the pink shaded area highlighting the DMR. DMR plots include 200 base pair flanking regions on each side of the DMR. DMRs identified in (e) brain and (f) liver were enriched in intergenic and inter-CpG regions, whilst being underrepresented in CpG and gene regions. The bar plot compares the number of whole-genome bisulfite sequencing (WGBS) DMRs in red to a set of equivalent randomly generated regions in blue. (g) Gene ontology analysis of liver DMRs shows enrichment within neuronal cellular components and biological processes. BP/red point = biological process, CC/blue point = cellular component. X-axis of point indicates FDR of ontology. Size of point indicates number of overlapping genes with ontology. There were insufficient number of DMRs identified in the brain for a gene ontology analysis.

Lower DNA methylation with early moderate PAE in NC mice was more frequently observed in liver DMRs (93.5% of liver DMRs), while brain DMRs were almost equally divided between lower and higher DNA methylation with early moderate PAE (52.6% of brain DMRs had lower DNA methylation with early moderate PAE). Some DMRs localised to the same genes in both brain and liver, although they were different regions. The three genes affected by PAE in both brain and the liver tissues were the Autism Susceptibility Gene 2 (Auts2), Androglobin (Adgb), and RNA Binding Protein Fox 1 (Rbfox1) genes (Table 1). In both brain and liver tissues, DMRs were enriched in non-coding intergenic and open sea regions and relatively underrepresented in coding and CpG island regions (Figure 5e and f). Using open chromatin assay and histone modification datasets from the ENCODE project, we found enrichment (p<0.05) of DMRs in open chromatin regions (ATAC-seq), enhancer regions (H3K4me1), and active gene promoter regions (H3K27ac), in mouse fetal forebrain tissue and fetal liver (Table 2). Gene ontology enrichment analysis of liver DMRs that did localise to genes showed enrichment in 10 predominantly neuronal pathways, with neuron projection being the most significant (Figure 5g, Supplementary file 1c and d).

Table 1
Table of differentially methylated regions (DMRs) identified in the intronic regions of genes that contained DMRs in both the brain and liver.

Δmeth indicates the percentage change in average methylation level within the DMR with prenatal alcohol exposure (PAE) compared to non-PAE mice.

GeneTissueIntronic DMRWidthNo. CpGsΔmethp-Value
Auts2Brainchr5:131510296–1315104651705–23.5%<0.05
Auts2Liverchr5:131621828–1316219991724–22.5%<0.05
AdgbBrainchr10:10455557–104558833274–25.0%<0.05
AdgbLiverchr10:10353338–103536132764–25.9%<0.05
Rbfox1Brainchr16:6813039–68132171795–24.3%<0.05
Rbfox1Liverchr16:6781985–67823303465–22.6%<0.05
Table 2
Number and percentage of brain and liver differentially methylated regions (DMRs) that overlap with tissue-specific regulatory regions.

ATAC-seq, H3K4me1, and H3K27ac regions were obtained at 0 days postnatal from the ENCODE database. p-Values for permutation testing using a randomisation strategy.

Assay typeBrain DMRsBrain randomised regionsLiver DMRsLiver randomised regions
ATAC-seq21/78 (26.92%), p=0.011/78 (1.28%), p=0.1653/759 (6.98%)
p=0.01		22/759 (2.90%)
p=0.31
H3K4me14/78 (5.13%)
p=0.03		2/78 (2.56%)
p=0.18		38/759 (5.01%)
p=0.05		35/759 (4.61%)
p=0.32
H3K27ac9/78 (11.54%)
p=0.01		2/78 (2.56%)
p=0.74		48/759 (6.32%)
p=0.01		19/759 (2.50%)
p=0.26

HMD mitigates the effects of early moderate PAE on DNA methylation

To determine whether administration of an HMD throughout pregnancy could mitigate the effects of PAE on offspring DNA methylation, we examined alcohol-sensitive DMRs identified in the previous analysis in the HMD mice. Compared to control mice (H2O+NC), PAE+HMD mice exhibited significant (p<0.05) DNA methylation differences in only 12/78 (15%) brain (Supplementary file 1g), and 124/759 (16%) liver (Supplementary file 1h) DMRs, suggesting the effects were predominantly mitigated. Effect sizes compared to mice on the normal chow were substantially lower, in some cases more than 25% reduced in mice on the HMD diet (Figure 6).

Figure 6
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High methyl donor (HMD) partially mitigated effects of prenatal alcohol exposure (PAE) on offspring DNA methylation.

Average DNA methylation effect sizes above 30% with PAE were observed in some (a) brain and (b) liver differentially methylated regions (DMRs) in normal chow (NC) mice. Mean absolute difference in methylation with PAE is reduced within the HMD mice in (c) brain and (d) liver. Each point represents one DMR. Point colour indicates change in DNA methylation with PAE. Points with a high number of cytosine-guanines (CpGs) and methylation difference are annotated with associated gene if located within a genic region. HMD was associated with (e) higher methylation in the DMR identified proximal to Lamb1 on chromosome 12 in brain and (f) lower methylation in the DMR identified proximal to Socs5 on chromosome 17 in liver. Each plot represents a separate treatment group. Each blue vertical line indicates a CpG site, with the height and corresponding left y-axis indicating the methylation ratio. The grey line and corresponding right y-axis indicate coverage at each CpG site. The black horizontal line indicates (e) 40% and (f) 80% methylation for comparison purposes. The x-axis indicates the base position on the chromosome, with the pink shaded area highlighting the DMR. DMR plots include 200 base pair flanking regions on each side of the DMR.

Effects of early moderate PAE and HMD on behavioural outcomes in adult mice

Remaining littermates from each treatment group were reared to adulthood and underwent behavioural testing assessing various neurocognitive domains that can be affected in FASD including locomotor activity, anxiety, spatial recognition, memory, motor coordination, and balance. There was no evidence that early moderate PAE had a significant effect on any of the behavioural outcomes tested (Figure 7). Mice exposed to HMD exhibited greater locomotor activity, in terms of distance travelled (Figure 8).

Figure 7
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PAE had no significant effect on other assessed behavioural outcomes.

PAE and HMD had no significant effect on anxiety as evident by no significant difference by unpaired t-test in the (a) percent time in the inner zone in the open field test (N=104) and (b) percent time open arms in the elevated plus maze test (N=85). PAE and HMD had no significant effect on spatial recognition as evident by no significant difference by unpaired t-test in the discrimination index in (c) object recognition (N=108) and (d) object in place test (N=98). PAE and HMD had no significant effect on motor coordination and balance as evident by no significant difference by unpaired t-test in times in (e) first rotarod test (N=112) and (f) second rotarod test (N=87). Bars show mean and standard deviation. Each point represents one mouse. NC = normal chow, HMD = high methyl diet, PAE = prenatal alcohol exposure. Time interval for each mouse was (a–c) 300 s and (d) 180 s.

Figure 8
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HMD was associated with increased locomotor activity.

HMD was associated with increased locomotor activity compared to NC, indicated by significantly greater total distance travelled in the (a) open field test (N=104), (b) object recognition test (N=108), (c) elevated plus maze test (N=88), and (d) object in place test (N=98) by unpaired t-test. Bars show mean and standard deviation. Each point represents one mouse. NC = normal chow, HMD = high methyl diet, PAE = prenatal alcohol exposure. Time interval for each mouse was (a–c) 300 s and (d) 180 s.

Replication studies in human PAE and FASD case-control cohorts

We undertook validation studies by examining PAE-sensitive regions identified in our murine model using existing DNA methylation data from human cohorts to address the generalizability of our findings. Only 36 of the 78 (46.2%) brain DMRs, and 294 of the 759 (38.8%) liver DMRs, had homologous regions in the human genome that were able to be tested. In this validation study, DNA methylation array data from 147 newborn buccal swabs from the Asking Questions About Alcohol in Pregnancy (AQUA) cohort (Muggli et al., 2022) were available from this cohort (96 moderate PAE and 51 controls). We performed differential testing on a total of 1898 CpG sites that corresponded to mouse DMRs, comparing ‘never exposed’ newborns to ‘any exposure’ and found no evidence of differential DNA methylation at these CpG (data not shown). We also accessed publicly available DNA methylation array measurements from buccal swabs taken from a Canadian clinical cohort of children with diagnosed FASD and controls (GSE109042). To avoid confounding due to ancestry, we analysed the 118 Caucasian individuals (30 FASD and 88 controls). Differential testing of a total of 2316 CpG sites that were homologous to mouse DMRs statistically replicated seven DMR associations with FASD status (FDR p<0.05) after adjusting for participant age, sex, array number, and estimated cell counts (Table 3). Visual comparisons of DNA methylation across these seven DMRs revealed striking differences in effect sizes between people with FASD and our murine model (Figure 9). Genes associated with these DMRs are linked to clinically relevant traits in the GWAS catalogue including facial morphology (GADD45A; Indencleef et al., 2021), educational attainment (AP2B1; Okbay et al., 2022), intelligence (RP9; Davies et al., 2019), autism and schizophrenia (ZNF823; Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium, 2017).

Figure 9
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Seven prenatal alcohol exposure (PAE) differentially methylated regions (DMRs) identified in the murine model were successfully replicated in the Lussier et al., 2018 human fetal alcohol spectrum disorder (FASD) cohort.

Examples of two PAE DMRs that had significantly lower DNA methylation with a clinical diagnosis of FASD in the Lussier et al., 2018 cohort (a and c), while their mouse liftover DMR also had significantly lower DNA methylation with PAE in the murine model experiment (b and d).

Table 3
Differentially methylated regions (DMRs) identified in the murine model that were validated in the Lussier et al., 2018 human case-control cohort for a clinical diagnosis of fetal alcohol spectrum disorder (FASD).

The upper section describes properties of Lussier et al., 2018 human DMRs. The lower section describes properties of the equivalent murine model DMRs.

DMROrganismTissueChrStartEndWidthNo. CpGsFDRMeandiffGene
1HumanBuccal1681515716815231074050.028636–0.00497GADD45A
2HumanBuccal1913000782130023571576110.000197–0.00203GCDH
3HumanBuccal73314881533149316502110.001149–0.00011RP9
4HumanBuccal173390544433905888445140.000171–0.00359AP2B1, PEX12
5HumanBuccal172718150327182342840110.018536–0.00246ERAL1, FAM222B
6HumanBuccal19129921811299247929990.037431–0.00179CTD-2265O21.7, DNASE2
7HumanBuccal19118495311185001348390.022724–0.00244ZNF823
1MouseLiver667034885670350821974<0.05–0.220833E230016M11Rik
2MouseLiver884901298849015442465<0.05–0.234457Klf1
3MouseLiver92245383622453893575<0.05–0.226427Rp9
4MouseBrain142140357021403622524<0.05–0.234193Adk
5MouseLiver1178069463780700025399<0.05–0.255864Mir144, Mir451a
6MouseLiver1178072079780723132344<0.05–0.215227Mir144, Mir451a
7MouseLiver217709192717709294510185<0.05–0.224354Intergenic

Candidate gene analysis of previously defined alcohol-sensitive regions

We also undertook a replication analysis in our murine data of previously published alcohol-sensitive regions by undertaking a systematic review of previously published mammalian studies (Bestry et al., 2022). Candidate gene studies identified 21 CpG sites (FDR<0.05) in the brain from 15,132 CpG sites tested, including two sites in the Mest (Peg1) gene and 19 sites in Kcnq1 (KvDMR1) (Supplementary file 1i). There were nine FDR-significant CpG sites identified in the liver out of 15,382 CpG sites tested, all of which were in Peg3 (Supplementary file 1j). All FDR-significant CpG sites from both tissues had higher DNA methylation in mice with PAE.

Discussion

In this study, we found that moderate early (first trimester) PAE was sufficient to induce site-specific differences to DNA methylation in newborn pups without causing overt behavioural outcomes in adult mice. Although global levels of DNA methylation were not significantly different with PAE, regional analysis demonstrated widespread effects characterised predominantly by lower DNA methylation with PAE, mostly at non-coding regions of the genome. In our model, alcohol effects on DNA methylation were predominantly tissue-specific, with only two genomic regions and four genes that were similarly affected in both liver and brain. These perturbations may have been established stochastically because of PAE to the early embryo and maintained in the differentiating tissue. Further analysis in different germ layer tissues is required to formally establish this. Indeed, most of the observed effects were tissue-specific, with more perturbations to the epigenome observable in liver tissue, which may reflect the liver’s specific role in metabolic detoxification of alcohol. Alternatively, cell-type composition differences between brain and liver might explain differential sensitivity to alcohol effects. Generally, DMRs were enriched in non-coding regions of the genome with regulatory potential, suggesting alcohol has broad effects on genome regulation.

Both the human replication studies and the candidate gene analysis provide validity to our model for recapitulating some of the genomic disturbances reported in patients with clinical FASD. It is remarkable that some associations identified in our murine model of early moderate exposure were recapitulated in human subjects with FASD despite species and biosample differences, suggesting that at least some DNA methylation changes are stable over time. Notably the effect size for replicated regions were strikingly smaller in blood samples from subjects with FASD suggesting the dose and duration of exposure may need to exceed a high threshold to survive reprogramming in the blood. We speculate this may explain lack of reproducibility in the AQUA cohort.

In the candidate gene analysis we replicated previously published reports of decreased DNA methylation within Peg3 and KvDMR1 from South African children with FAS (Masemola et al., 2015). Both genes are methylated in a parent-of-origin specific manner, suggesting that alcohol may affect imprinting processes. Previous rodent and human studies have identified DNA methylation differences with PAE in imprinted regions such as the Igf2/H19 locus (Portales-Casamar et al., 2016; Downing et al., 2011; Zhou et al., 2016), although results are not entirely consistent (Marjonen et al., 2018; Stouder et al., 2011). On the balance of this, we speculate duration of exposure, dose, and other tissue-related factors all likely influence the extent to which genome regulation is perturbed and manifests as differences in DNA methylation.

Our results are encouraging for biomarker studies and aid in the prioritisation of associations for future follow-up, particularly in relation to diagnosis of FASD. For example, three genes that were validated in the Lussier et al., 2018 cohort are zinc finger proteins (RP9, PEX12, and ZNF823) that play an important role in fetal gene regulation. Notably, PEX12 is associated with Zellweger syndrome, which is a rare peroxisome biogenesis disorder (the most severe variant of peroxisome biogenesis disorder spectrum), characterised by neuronal migration defects in the brain, dysmorphic craniofacial features, profound hypotonia, neonatal seizures, and liver dysfunction (Konkoľová et al., 2015).

Future studies could perform transcriptomic analysis to investigate. Another key finding from this study was that HMD mitigated some of the effects of PAE on DNA methylation. Although a plausible alternative explanation is that some of the PAE regions were not reproduced in the set of mice given the folate diet, our data are consistent with preclinical studies of choline supplementation in rodent models (Thomas et al., 2007; Thomas et al., 2000; Otero et al., 2012). Moreover, a subset of PAE regions were statistically replicated in subjects with FASD, suggestive of robust associations. Although our findings should be interpreted with caution, they collectively support the notion that alcohol-induced perturbation of epigenetic regulation may occur, at least in part, through disruption of the one-carbon metabolism. The most encouraging aspect of this relates to the potential utility for evidence-informed recommendations for dietary advice or supplementation, particularly in population groups with limited access to antenatal care or healthy food choices.

Strengths of this study include the use of controlled interventions coupled with comprehensive assessment of the effects of PAE on multiple tissues. We also performed WGBS representing the gold standard in DNA methylation analysis, which to our knowledge has not been performed before in the context of murine PAE studies. Our findings were partially generalisable in replication studies addressing the robustness of our experimental approach. Caveats of our study design include a limited ability to determine the contribution of specific cell types within tissues to the methylation differences observed, and we did not assess markers of brain or liver physiology. Additionally, we employed an ad libitum alcohol exposure model rather than direct dosing of dams. Although the trajectories of alcohol consumption were not statistically different between groups, this introduces more variability into alcohol exposure patterns, and might impact offspring methylation data. Despite these limitations, the results were meaningful in the context of typical patterns of alcohol consumption in human populations.

In conclusion, this study demonstrates that early moderate PAE can disturb fetal genome regulation in mice and humans and supports current public health advice that alcohol consumption during pregnancy, even at low doses, may be harmful.

Materials and methods

Murine subjects and housing

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To study the effects of early moderate PAE on offspring DNA methylation processes, we adapted a murine model study design that has previously reported DNA methylation changes at the Avy locus in Agouti mice (Kaminen-Ahola et al., 2010; Figure 1). This study received animal ethics approval from the Telethon Kids Institute Animal Ethics Committee (Approval Number: 344). Sixty nulliparous C57BL/6J female mice aged ~8 weeks were mated with equivalent stud male mice. Pregnant dams were randomly assigned to one of four treatment groups (n=15 dams per group) that varied based on composition of the drinking water and chow given to the dams:

  1. PAE-NC (prenatal alcohol exposure-normal chow): 10% (vol/vol) ethanol in non-acidified water ad libitum from 10 days prior to mating until gestational days (GD) 8–10. This is intended to replicate typical patterns of drinking during the first trimester of pregnancy in humans. Dams received non-acidified reverse osmosis water for the remainder of pregnancy and normal chow (Rat and Mouse Cubes, Speciality Feeds, Glen Forrest, Australia) throughout pregnancy.

  2. PAE-HMD (prenatal alcohol exposure-high methyl donor diet): 10% (vol/vol) ethanol in non-acidified water ad libitum from 10 days prior to mating until GD8-10 and non-acidified reverse osmosis water for remainder of pregnancy. Isocaloric HMD chow consisting of 20 mg/kg folate and 4970 mg/kg choline throughout pregnancy (Speciality Feeds, Glen Forrest, Australia).

  3. H2O-NC (water-normal chow): non-acidified water and normal chow throughout pregnancy.

  4. H2O-HMD (water-high methyl donor diet): non-acidified water and HMD chow throughout pregnancy.

WGBS of newborn mouse tissues

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Pups selected for WGBS in each intervention group were matched on sex and litter size to minimize variability in exposure. Two male and two female pups per treatment group (n=16 total) were euthanised by intraperitoneal injection with ketamine and xylazine on the day of birth for WGBS of their brain and liver tissues. Mouse tissue samples were stored at –80°C. Remaining littermates grew until adulthood for behavioural testing. Ten milligrams of tissue were collected from each liver and brain and lysed in Chemagic RNA Tissue10 Kit special H96 extraction buffer. Total nucleic acid was extracted from the tissues using the Chemagic 360 instrument (PerkinElmer) and quantified with Qubit DNA High Sensitivity Kit (Catalogue Number: Q32854, Thermo Scientific). 100 ng of genomic DNA was spiked with 0.5 ng of unmethylated lambda DNA (Catalogue Number: D1521, Promega) to assess the bisulfite conversion efficiency. Each sample was digested with 2 µl RNase A (Invitrogen) at 37°C for 20 min to remove RNA. 100 ng of genomic DNA from each sample was sheared using a Covaris M220 (300 bp settings, Covaris). Libraries were prepared using the Lucigen NxSeq AmpFREE Low DNA Library Kit (Catalogue Number: 14000-1, Lucigen), according to the manufacturer’s instructions. Nextflex bisulfite-seq barcodes (Catalogue Number: Nova-511913, PerkinElmer) were used as the adapters with incubation at 25°C for 30 min. The libraries were bisulfite converted using the Zymo EZ DNA Methylation-Gold Kit (Catalogue Number: D5005, Zymo Research) and PCR amplified using the KAPA HiFi Uracil PCR Kit (Catalogue Number: ROC-07959052001, Kapa Biosystems). The final libraries were assessed with the Agilent 2200 Tapestation System using D1000 Kit (Catalogue Number: 5067-5582). WGBS was performed by Genomics WA sequencing core on a NovaSeq 6000 (Illumina) using 2×150 bp chemistry on an S4 flow cell. The bisulfite conversion rate in each tissue sample was at least 99%. The overall mean coverage in each sample was 9.69× (range: 6.51–12.12×).

Behavioural testing in adult mice

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Littermates who were not sacrificed at birth were reared on normal chow and drinking water ad libitum until adulthood (~8 weeks after birth) when they underwent behavioural tests assessing five neurodevelopmental domains that can be affected by PAE including locomotor activity, anxiety, spatial recognition, memory, motor coordination, and balance. These tests included the open field test (locomotor activity, anxiety) (Seibenhener and Wooten, 2015), object recognition test (locomotor activity, spatial recognition) (Lueptow, 2017), object in place test (locomotor activity, spatial recognition) (Murai et al., 2007), elevated plus maze test (locomotor activity, anxiety) (Komada et al., 2008), and two trials of the rotarod test (motor coordination, balance) (Deacon, 2013). Between mouse subjects, behavioural testing equipment was cleaned with 70% ethanol. Video recording was employed for all behavioural tests, except for the rotarod, and the assessment process was semi-automated using ANY-maze software (Stoelting Co., Wood Dale, IL, USA).

Statistical analysis

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Dam characteristics and pup behavioural testing results were generally assessed using unpaired t-tests comparing each treatment group to the baseline control group that was given non-acidified reverse osmosis water and normal chow throughout pregnancy. Trajectories of liquid consumption and weight gain across pregnancy were assessed using a quadratic mixed effects model and the trajectory of chow consumption across pregnancy was assessed using a linear mixed effects model. To examine the effect of alcohol exposure on behavioural outcomes we used linear regression with alcohol group (binary) as the main predictor adjusted for diet and sex. For sequencing data, raw fastq files were mapped to the mm10 mouse reference genome with BSseeker 2 (version 2.1.8) (Guo et al., 2013) and CG-maptools (version number 0.1.2) (Guo et al., 2018) using a custom bioinformatics pipeline. CGmap output files were combined as a bsseq object in the R statistical environment (R Development Core Team, 2021). We filtered the sex chromosomal reads and then combined reads from mice in the same treatment group using the collapseBSseq function, to maximise coverage prior to differential DNA methylation analysis. CpG sites with an aggregated coverage below 10× in each tissue type were removed prior to modelling to ensure there was sufficient coverage in all assessed CpG sites. This retained 94.9% of CpG sites in the brain and 93.8% of CpG sites in the liver. DMRs were identified within each tissue using a Bayesian hierarchical model comparing average DNA methylation ratios in each CpG site between PAE and non-PAE mice using the Wald test with smoothing, implemented in the R package DSS (Wu et al., 2015). False discovery rate (FDR) control was achieved through shrinkage estimation methods. We declared DMRs as those with a local FDR p-value<0.05 based on the p-values of each individual CpG site in the DMR, and minimum mean effect size (delta) of 5%. Gene ontology analysis was performed on the brain and liver DMRs using the gene set enrichment analysis computational method (Subramanian et al., 2005) to determine if the DMRs were associated with any transcription start sites or biological processes. Brain and liver DMRs were tested for enrichment within ENCODE Project datasets (Luo et al., 2020) by an overlap permutation test with 100 permutations using the regioneR package. The ENCODE Project datasets that were assessed included ENCFF845WSI, ENCFF764NTQ, ENCFF937JHP, ENCFF269TLO, ENCFF676TSV, and ENCFF290MLR. DMRs were then tested for enrichment within specific genic and CpG regions of the mouse genome, compared to a randomly generated set of regions in the mouse genome generated with resampleRegions in regioneR, with equivalent means and standard deviations. For candidate gene analysis, we compiled a set of key genes and genomic regions identified in previous mammalian PAE studies for site-specific testing based on our prior systematic review (Bestry et al., 2022), which identified 37 candidate genes (Supplementary file 1e and f). Murine brain and liver datasets were filtered to candidate gene regions and differential testing was then performed across the entire coding sequence, separately in the brain and liver of the mice on a normal diet using the callDML feature in DSS.

Validation studies in human cohorts

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We used existing human datasets to validate observations from our murine model (GSE109042), focusing on regions identified in our early moderate PAE model. Validation studies in human cohorts with existing genome-wide DNA methylation datasets and matching PAE data are described in the Supplementary Material. Briefly, Illumina Human Methylation array. iDAT files were pre-processed using the minfi package (Aryee et al., 2014) from the Bioconductor project (http://www.bioconductor.org) in the R statistical environment (http://cran.r-project.org/, version 4.2.2). Sample quality was assessed using control probes on the array. Between-array normalization was performed using the stratified quantile method to correct for Type 1 and Type 2 probe bias. Probes exhibiting a p-detection call rate of >0.01 in one or more samples were removed prior to analysis. Probes containing SNPs at the single base extension site, or at the CpG assay site were removed, as were probes measuring non-CpG loci (32,445 probes). Probes reported to have off-target effects in McCartney et al., 2016, were also removed. Mouse DMRs were converted into human equivalent regions using an mm10 to hg19 genome conversion with the liftover tool in the UCSC Genome Browser (Kent et al., 2002). A minimum 0.1 ratio of bases that must remap was specified as recommended for liftover between regions from different species and multiple output regions were allowed. Differential testing of candidate mouse DMRs was carried out using the R package DMRcate (Peters et al., 2021) for each dataset and DMRs were declared as minimum smoothed FDR<0.05. Cell heterogeneity in each sample including the composition of epithelial, fibroblast, and immune cells was estimated from DNA methylation reads using the R package EpiDISH (Teschendorff et al., 2017).

Data availability

The mouse WGBS data are deposited into the GEO database under accession number GSE273157.

The following data sets were generated
    1. Martino DJ
    (2024) NCBI Gene Expression Omnibus
    ID GSE273157. Early Moderate Prenatal Alcohol Exposure and Maternal Diet Impact Offspring DNA Methylation Across Species.
    https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE273157

References

    1. Davies G
    2. Lam M
    3. Harris SE
    4. Trampush JW
    5. Luciano M
    6. Hill WD
    7. Hagenaars SP
    8. Ritchie SJ
    9. Marioni RE
    10. Fawns-Ritchie C
    11. Liewald DCM
    12. Okely JA
    13. Ahola-Olli AV
    14. Barnes CLK
    15. Bertram L
    16. Bis JC
    17. Burdick KE
    18. Christoforou A
    19. DeRosse P
    20. Djurovic S
    21. Espeseth T
    22. Giakoumaki S
    23. Giddaluru S
    24. Gustavson DE
    25. Hayward C
    26. Hofer E
    27. Ikram MA
    28. Karlsson R
    29. Knowles E
    30. Lahti J
    31. Leber M
    32. Li S
    33. Mather KA
    34. Melle I
    35. Morris D
    36. Oldmeadow C
    37. Palviainen T
    38. Payton A
    39. Pazoki R
    40. Petrovic K
    41. Reynolds CA
    42. Sargurupremraj M
    43. Scholz M
    44. Smith JA
    45. Smith AV
    46. Terzikhan N
    47. Thalamuthu A
    48. Trompet S
    49. van der Lee SJ
    50. Ware EB
    51. Windham BG
    52. Wright MJ
    53. Yang J
    54. Yu J
    55. Ames D
    56. Amin N
    57. Amouyel P
    58. Andreassen OA
    59. Armstrong NJ
    60. Assareh AA
    61. Attia JR
    62. Attix D
    63. Avramopoulos D
    64. Bennett DA
    65. Böhmer AC
    66. Boyle PA
    67. Brodaty H
    68. Campbell H
    69. Cannon TD
    70. Cirulli ET
    71. Congdon E
    72. Conley ED
    73. Corley J
    74. Cox SR
    75. Dale AM
    76. Dehghan A
    77. Dick D
    78. Dickinson D
    79. Eriksson JG
    80. Evangelou E
    81. Faul JD
    82. Ford I
    83. Freimer NA
    84. Gao H
    85. Giegling I
    86. Gillespie NA
    87. Gordon SD
    88. Gottesman RF
    89. Griswold ME
    90. Gudnason V
    91. Harris TB
    92. Hartmann AM
    93. Hatzimanolis A
    94. Heiss G
    95. Holliday EG
    96. Joshi PK
    97. Kähönen M
    98. Kardia SLR
    99. Karlsson I
    100. Kleineidam L
    101. Knopman DS
    102. Kochan NA
    103. Konte B
    104. Kwok JB
    105. Le Hellard S
    106. Lee T
    107. Lehtimäki T
    108. Li SC
    109. Lill CM
    110. Liu T
    111. Koini M
    112. London E
    113. Longstreth WT
    114. Lopez OL
    115. Loukola A
    116. Luck T
    117. Lundervold AJ
    118. Lundquist A
    119. Lyytikäinen LP
    120. Martin NG
    121. Montgomery GW
    122. Murray AD
    123. Need AC
    124. Noordam R
    125. Nyberg L
    126. Ollier W
    127. Papenberg G
    128. Pattie A
    129. Polasek O
    130. Poldrack RA
    131. Psaty BM
    132. Reppermund S
    133. Riedel-Heller SG
    134. Rose RJ
    135. Rotter JI
    136. Roussos P
    137. Rovio SP
    138. Saba Y
    139. Sabb FW
    140. Sachdev PS
    141. Satizabal CL
    142. Schmid M
    143. Scott RJ
    144. Scult MA
    145. Simino J
    146. Slagboom PE
    147. Smyrnis N
    148. Soumaré A
    149. Stefanis NC
    150. Stott DJ
    151. Straub RE
    152. Sundet K
    153. Taylor AM
    154. Taylor KD
    155. Tzoulaki I
    156. Tzourio C
    157. Uitterlinden A
    158. Vitart V
    159. Voineskos AN
    160. Kaprio J
    161. Wagner M
    162. Wagner H
    163. Weinhold L
    164. Wen KH
    165. Widen E
    166. Yang Q
    167. Zhao W
    168. Adams HHH
    169. Arking DE
    170. Bilder RM
    171. Bitsios P
    172. Boerwinkle E
    173. Chiba-Falek O
    174. Corvin A
    175. De Jager PL
    176. Debette S
    177. Donohoe G
    178. Elliott P
    179. Fitzpatrick AL
    180. Gill M
    181. Glahn DC
    182. Hägg S
    183. Hansell NK
    184. Hariri AR
    185. Ikram MK
    186. Jukema JW
    187. Vuoksimaa E
    188. Keller MC
    189. Kremen WS
    190. Launer L
    191. Lindenberger U
    192. Palotie A
    193. Pedersen NL
    194. Pendleton N
    195. Porteous DJ
    196. Räikkönen K
    197. Raitakari OT
    198. Ramirez A
    199. Reinvang I
    200. Rudan I
    201. Schmidt R
    202. Schmidt H
    203. Schofield PW
    204. Schofield PR
    205. Starr JM
    206. Steen VM
    207. Trollor JN
    208. Turner ST
    209. Van Duijn CM
    210. Villringer A
    211. Weinberger DR
    212. Weir DR
    213. Wilson JF
    214. Malhotra A
    215. McIntosh AM
    216. Gale CR
    217. Seshadri S
    218. Mosley TH
    219. Bressler J
    220. Lencz T
    221. Deary IJ
    (2019) Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
    Nature Communications 10:2068.
    https://doi.org/10.1038/s41467-019-10160-w
  40. Software
    1. R Development Core Team
    (2021) R: A language and environment for statistical computing
    R Foundation for Statistical Computing, Vienna, Austria.
    https://www.r-project.org
    1. Zakhari S
    (2006)
    Overview: how is alcohol metabolized by the body?
    Alcohol Research & Health 29:245–254.
    1. Zhou JZ
    2. Qian YY
    3. Zhou QJ
    4. Xiong Y
    5. Wang HJ
    6. Ma D
    (2016)
    Tissue-specific differential DNA methylation at Igf2/H19 locus in a mouse model for embryonal ethanol exposure
    International Journal of Clinical and Experimental Pathology 9:4862–4871.

Article and author information

Author details

  1. Mitchell Bestry

    Telethon Kids Institute, The University of Western Australia, Perth, Australia
    Contribution
    Data curation, Formal analysis, Investigation, Methodology, Writing - original draft, Project administration
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-1962-7925

  2. Alexander N Larcombe

    1. Respiratory Environmental Health, Wal-yan Respiratory Research Centre, Telethon Kids Institute, Nedlands, Australia
    2. Occupation, Environment and Safety, School of Population Health, Curtin University, Perth, Australia
    Contribution
    Conceptualization, Data curation, Formal analysis, Supervision, Funding acquisition, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared

  3. Nina Kresoje

    Telethon Kids Institute, Nedlands, Australia
    Contribution
    Supervision, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared

  4. Emily K Chivers

    Respiratory Environmental Health, Wal-yan Respiratory Research Centre, Telethon Kids Institute, Nedlands, Australia
    Contribution
    Data curation, Methodology
    Competing interests
    No competing interests declared

  5. Chloe Bakker

    Respiratory Environmental Health, Wal-yan Respiratory Research Centre, Telethon Kids Institute, Nedlands, Australia
    Contribution
    Data curation, Investigation, Methodology
    Competing interests
    No competing interests declared

  6. James P Fitzpatrick

    School of Psychological Sciences, University of Western Australia, Perth, Australia
    Contribution
    Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared

  7. Elizabeth J Elliott

    1. University of Sydney, Faculty of Medicine and Health, Specialty of Child and Adolescent Health, Melbourne, Australia
    2. Sydney Children’s Hospitals Network (Westmead) and Kids Research, Geelong, Australia
    Contribution
    Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared

  8. Jeffrey M Craig

    1. Deakin University, IMPACT – the Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Geelong, Australia
    2. Murdoch Children’s Research Institute, Royal Children’s Hospital, Parkville, Australia
    3. Department of Paediatrics, University of Melbourne, Royal Children’s Hospital, Parkville, Australia
    Contribution
    Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3979-7849

  9. Evelyne Muggli

    1. Murdoch Children’s Research Institute, Royal Children’s Hospital, Parkville, Australia
    2. Department of Paediatrics, University of Melbourne, Royal Children’s Hospital, Parkville, Australia
    Contribution
    Data curation, Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared

  10. Jane Halliday

    1. Department of Paediatrics, University of Melbourne, Royal Children’s Hospital, Parkville, Australia
    2. Reproductive Epidemiology, Murdoch Children's Research Institute, Parkville, Australia
    Contribution
    Data curation, Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared

  11. Delyse Hutchinson

    1. Reproductive Epidemiology, Murdoch Children's Research Institute, Parkville, Australia
    2. Deakin University, School of Psychology, Faculty of Health, Geelong, Australia
    3. Murdoch Children’s Research Institute, Centre for Adolescent Health, Royal Children’s Hospital, Melbourne, Australia
    4. University New South Wales, National Drug and Alcohol Research Centre, Sydney, Australia
    Contribution
    Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared

  12. Sam Buckberry

    1. Telethon Kids Institute, Nedlands, Australia
    2. Harry Perkins Institute of Medical Research, QEII Medical Centre and Centre for Medical Research, The University of Western Australia, Perth, Australia
    3. ARC Centre of Excellence in Plant Energy Biology, School of Molecular Sciences, The University of Western Australia, Perth, Australia
    Contribution
    Supervision, Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-2388-6046

  13. Ryan Lister

    1. Harry Perkins Institute of Medical Research, QEII Medical Centre and Centre for Medical Research, The University of Western Australia, Perth, Australia
    2. ARC Centre of Excellence in Plant Energy Biology, School of Molecular Sciences, The University of Western Australia, Perth, Australia
    Contribution
    Supervision, Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-6637-7239

  14. Martyn Symons

    1. Telethon Kids Institute, The University of Western Australia, Perth, Australia
    2. National Drug Research Institute, enAble Institute, Curtin University, Perth, Australia
    Contribution
    Conceptualization, Supervision, Funding acquisition, Writing – review and editing
    Competing interests
    No competing interests declared

  15. David Martino

    Wal-yan Respiratory Research Centre, Telethon Kids Institute, Nedlands, Australia
    Contribution
    Conceptualization, Supervision, Project administration, Writing – review and editing
    For correspondence
    david.martino@telethonkids.org.au
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-6823-4696

Funding

National Health and Medical Research Council (114601)

  • James P Fitzpatrick
  • Elizabeth J Elliott
  • Martyn Symons

Department of Health, Government of Western Australia (WACRF2019/20 R8)

  • Alexander N Larcombe
  • James P Fitzpatrick
  • Elizabeth J Elliott
  • Jeffrey M Craig
  • Evelyne Muggli
  • Jane Halliday
  • Delyse Hutchinson
  • Sam Buckberry
  • Ryan Lister
  • Martyn Symons
  • David Martino

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We wish to acknowledge the assistance of Dr Jahnvi Pflueger who provided training on preparation of WGBS libraries. We wish to acknowledge the financial contribution of the Centre for Research Excellence in FASD who supported the murine experiments.

Ethics

This study received animal ethics approval from the Telethon Kids Institute Animal Ethics Committee (Approval Number: 344). All procedures were carried out in accordance with the approved protocol.

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Copyright

© 2023, Bestry et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. Mitchell Bestry
  2. Alexander N Larcombe
  3. Nina Kresoje
  4. Emily K Chivers
  5. Chloe Bakker
  6. James P Fitzpatrick
  7. Elizabeth J Elliott
  8. Jeffrey M Craig
  9. Evelyne Muggli
  10. Jane Halliday
  11. Delyse Hutchinson
  12. Sam Buckberry
  13. Ryan Lister
  14. Martyn Symons
  15. David Martino
(2024)
Early moderate prenatal alcohol exposure and maternal diet impact offspring DNA methylation across species
eLife 12:RP92135.
https://doi.org/10.7554/eLife.92135.3

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    Shannon H Carroll, Sogand Schafer ... Eric C Liao
    Research Article

    Wnt signaling plays crucial roles in embryonic patterning including the regulation of convergent extension (CE) during gastrulation, the establishment of the dorsal axis, and later, craniofacial morphogenesis. Further, Wnt signaling is a crucial regulator of craniofacial morphogenesis. The adapter proteins Dact1 and Dact2 modulate the Wnt signaling pathway through binding to Disheveled. However, the distinct relative functions of Dact1 and Dact2 during embryogenesis remain unclear. We found that dact1 and dact2 genes have dynamic spatiotemporal expression domains that are reciprocal to one another suggesting distinct functions during zebrafish embryogenesis. Both dact1 and dact2 contribute to axis extension, with compound mutants exhibiting a similar CE defect and craniofacial phenotype to the wnt11f2 mutant. Utilizing single-cell RNAseq and an established noncanonical Wnt pathway mutant with a shortened axis (gpc4), we identified dact1/2-specific roles during early development. Comparative whole transcriptome analysis between wildtype and gpc4 and wildtype and dact1/2 compound mutants revealed a novel role for dact1/2 in regulating the mRNA expression of the classical calpain capn8. Overexpression of capn8 phenocopies dact1/2 craniofacial dysmorphology. These results identify a previously unappreciated role of capn8 and calcium-dependent proteolysis during embryogenesis. Taken together, our findings highlight the distinct and overlapping roles of dact1 and dact2 in embryonic craniofacial development, providing new insights into the multifaceted regulation of Wnt signaling.

    1. Developmental Biology

    Extramacrochaetae regulates Notch signaling in the Drosophila eye through non-apoptotic caspase activity

    Sudershana Nair, Nicholas E Baker
    Research Article

    Many cell fate decisions are determined transcriptionally. Accordingly, some fate specification is prevented by Inhibitor of DNA-binding (Id) proteins that interfere with DNA binding by master regulatory transcription factors. We show that the Drosophila Id protein Extra macrochaetae (Emc) also affects developmental decisions by regulating caspase activity. Emc, which prevents proneural bHLH transcription factors from specifying neural cell fate, also prevents homodimerization of another bHLH protein, Daughterless (Da), and thereby maintains expression of the Death-Associated Inhibitor of Apoptosis (diap1) gene. Accordingly, we found that multiple effects of emc mutations on cell growth and on eye development were all caused by activation of caspases. These effects included acceleration of the morphogenetic furrow, failure of R7 photoreceptor cell specification, and delayed differentiation of non-neuronal cone cells. Within emc mutant clones, Notch signaling was elevated in the morphogenetic furrow, increasing morphogenetic furrow speed. This was associated with caspase-dependent increase in levels of Delta protein, the transmembrane ligand for Notch. Posterior to the morphogenetic furrow, elevated Delta cis-inhibited Notch signaling that was required for R7 specification and cone cell differentiation. Growth inhibition of emc mutant clones in wing imaginal discs also depended on caspases. Thus, emc mutations reveal the importance of restraining caspase activity even in non-apoptotic cells to prevent abnormal development, in the Drosophila eye through effects on Notch signaling.