4.5 Article

PCB126 Exposure Revealed Alterations in m6A RNA Modifications in Transcripts Associated With AHR Activation

期刊

TOXICOLOGICAL SCIENCES
卷 179, 期 1, 页码 84-94

出版社

OXFORD UNIV PRESS
DOI: 10.1093/toxsci/kfaa158

关键词

dioxin-like PCBs; development; zebrafish; epitranscriptomics; m6A; MeRIP

资金

  1. National Institute of Health National Institute of Environmental Health Sciences Outstanding New Environmental Scientist [NIH R01ES024915]
  2. Woods Hole Center for Oceans and Human Health [National Institutes of Health (NIH)] [P01ES028938]
  3. National Science Foundation [OCE-1840381]

向作者/读者索取更多资源

This study investigated the acute effects of environmental chemical exposure on m6A methylation patterns, revealing that dioxin-like PCBs could potentially alter developmental gene expression patterns by affecting m6A levels. Further studies are needed to understand the functional consequences of exposure-associated alterations in m6A levels.
Chemical modifications of proteins, DNA, and RNA moieties play critical roles in regulating gene expression. Emerging evidence suggests the RNA modifications (epitranscriptomics) have substantive roles in basic biological processes. One of the most common modifications in mRNA and noncoding RNAs is N-6-methyladenosine (m6A). In a subset of mRNAs, m6A sites are preferentially enriched near stop codons, in 30 UTRs, and within exons, suggesting an important role in the regulation of mRNA processing and function including alternative splicing and gene expression. Very little is known about the effect of environmental chemical exposure on m6A modifications. As many of the commonly occurring environmental contaminants alter gene expression profiles and have detrimental effects on physiological processes, it is important to understand the effects of exposure on this important layer of gene regulation. Hence, the objective of this study was to characterize the acute effects of developmental exposure to PCB126, an environmentally relevant dioxin-like PCB, on m6A methylation patterns. We exposed zebrafish embryos to PCB126 for 6h starting from 72h post fertilization and profiled m6A RNA using methylated RNA immunoprecipitation followed by sequencing (MeRIP-seq). Our analysis revealed 117 and 217 m6A peaks in the DMSO and PCB126 samples (false discovery rate 5%), respectively. The majority of the peaks were preferentially located around the 30 UTR and stop codons. Statistical analysis revealed 15 m6A marked transcripts to be differentially methylated by PCB126 exposure. These include transcripts that are known to be activated by AHR agonists (eg, ahrra, tiparp, nfe2l2b) as well as others that are important for normal development (vgf, cebpd, sned1). These results suggest that environmental chemicals such as dioxin-like PCBs could affect developmental gene expression patterns by altering m6A levels. Further studies are necessary to understand the functional consequences of exposure-associated alterations in m6A levels.

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