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Altered gene expression linked to germline dysfunction following exposure of Caenorhabditis elegans to DEET
N,N-diethyl-meta-toluamide (DEET) is a commonly used synthetic insect repellent. Although the neurological effects of DEET have been widely investigated, its effects on the germline are less understood. Here, we show that exposure of the nematode Caenorhabditis elegans, which is highly predictive of...
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Published in: | iScience 2024-01, Vol.27 (1), p.108699-108699, Article 108699 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | N,N-diethyl-meta-toluamide (DEET) is a commonly used synthetic insect repellent. Although the neurological effects of DEET have been widely investigated, its effects on the germline are less understood. Here, we show that exposure of the nematode Caenorhabditis elegans, which is highly predictive of mammalian reprotoxicity, resulting in internal DEET levels within the range detected in human biological samples, causes activation of p53/CEP-1-dependent germ cell apoptosis, altered meiotic recombination, chromosome abnormalities, and missegregation. RNA-sequencing analysis links DEET-induced alterations in the expression of genes related to redox processes and chromatin structure to reduced mitochondrial function, impaired DNA double-strand break repair progression, and defects during early embryogenesis. We propose that Caenorhabditis elegans exposure to DEET interferes with gene expression, leading to increased oxidative stress and altered chromatin structure, resulting in germline effects that pose a risk to reproductive health.
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•C. elegans DEET levels, within the range in many human samples, impairs meiosis•DEET compromises genomic integrity by deregulating meiotic recombination•DEET exposure causes chromosomal abnormalities and impairs early embryogenesis•Redox and chromatin genes link DEET to mitochondrial and germline dysfunction
Biological sciences; Environmental toxicology; Molecular toxicology; Cell biology |
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ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2023.108699 |