» Articles » PMID: 36035158

Elevated Exposures to Persistent Endocrine Disrupting Compounds Impact the Sperm Methylome in Regions Associated with Autism Spectrum Disorder

Overview
Journal Front Genet
Date 2022 Aug 29
PMID 36035158
Authors
Affiliations
Soon will be listed here.
Abstract

Environmental exposures to endocrine disrupting compounds (EDCs) such as the organochlorines have been linked with various diseases including neurodevelopmental disorders. Autism spectrum disorder (ASD) is a highly complex neurodevelopmental disorder that is considered strongly genetic in origin due to its high heritability. However, the rapidly rising prevalence of ASD suggests that environmental factors may also influence risk for ASD. In the present study, whole genome bisulfite sequencing was used to identify genome-wide differentially methylated regions (DMRs) in a total of 52 sperm samples from a cohort of men from the Faroe Islands (Denmark) who were equally divided into high and low exposure groups based on their serum levels of the long-lived organochlorine 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (DDE), a primary breakdown product of the now banned insecticide dichlorodiphenyltrichloroethane (DDT). Aside from being considered a genetic isolate, inhabitants of the Faroe Islands have a native diet that potentially exposes them to a wide range of seafood neurotoxicants in the form of persistent organic pollutants (POPs). The DMRs were mapped to the human genome using Bismark, a 3-letter aligner used for methyl-seq analyses. Gene ontology, functional, and pathway analyses of the DMR-associated genes showed significant enrichment for genes involved in neurological functions and neurodevelopmental processes frequently impacted by ASD. Notably, these genes also significantly overlap with autism risk genes as well as those previously identified in sperm from fathers of children with ASD in comparison to that of fathers of neurotypical children. These results collectively suggest a possible mechanism involving altered methylation of a significant number of neurologically relevant ASD risk genes for introducing epigenetic changes associated with environmental exposures into the sperm methylome. Such changes may provide the potential for transgenerational inheritance of ASD as well as other disorders.

Citing Articles

Intercontinental insights into autism spectrum disorder: a synthesis of environmental influences and DNA methylation.

Kuodza G, Kawai R, LaSalle J Environ Epigenet. 2024; 10(1):dvae023.

PMID: 39703685 PMC: 11658417. DOI: 10.1093/eep/dvae023.


Generational stability of epigenetic transgenerational inheritance facilitates adaptation and evolution.

Korolenko A, Skinner M Epigenetics. 2024; 19(1):2380929.

PMID: 39104183 PMC: 11305060. DOI: 10.1080/15592294.2024.2380929.


Reproductive toxicity of combined effects of endocrine disruptors on human reproduction.

Dutta S, Sengupta P, Bagchi S, Chhikara B, Pavlik A, Slama P Front Cell Dev Biol. 2023; 11:1162015.

PMID: 37250900 PMC: 10214012. DOI: 10.3389/fcell.2023.1162015.


Epigenetic changes in sperm are associated with paternal and child quantitative autistic traits in an autism-enriched cohort.

Feinberg J, Schrott R, Ladd-Acosta C, Newschaffer C, Hertz-Picciotto I, Croen L Mol Psychiatry. 2023; 29(1):43-53.

PMID: 37100868 DOI: 10.1038/s41380-023-02046-7.

References
1.
Moosa A, Shu H, Sarachana T, Hu V . Are endocrine disrupting compounds environmental risk factors for autism spectrum disorder?. Horm Behav. 2017; 101:13-21. PMC: 5913002. DOI: 10.1016/j.yhbeh.2017.10.003. View

2.
Osumi N, Tatehana M . Transgenerational epigenetic information through the sperm: Sperm cells not just merely supply half of the genome for new life; they also seem to transmit additional information via epigenetic modifications. EMBO Rep. 2021; 22(8):e53539. PMC: 8344929. DOI: 10.15252/embr.202153539. View

3.
Faulk C, Kim J, Jones T, McEachin R, Nahar M, Dolinoy D . Bisphenol A-associated alterations in genome-wide DNA methylation and gene expression patterns reveal sequence-dependent and non-monotonic effects in human fetal liver. Environ Epigenet. 2016; 1(1). PMC: 4922640. DOI: 10.1093/eep/dvv006. View

4.
Ellefsen A, Kampmann H, Billstedt E, Gillberg I, Gillberg C . Autism in the Faroe Islands: an epidemiological study. J Autism Dev Disord. 2006; 37(3):437-44. DOI: 10.1007/s10803-006-0178-y. View

5.
Mohrmann I, Gillessen-Kaesbach G, Siebert R, Caliebe A, Hellenbroich Y . A de novo 0.57 Mb microdeletion in chromosome 11q13.1 in a patient with speech problems, autistic traits, dysmorphic features and multiple endocrine neoplasia type 1. Eur J Med Genet. 2011; 54(4):e461-4. DOI: 10.1016/j.ejmg.2011.04.006. View