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Modulation of the Drosophila transcriptome by developmental exposure to alcohol

BACKGROUND: Prenatal exposure to ethanol can cause fetal alcohol spectrum disorder (FASD), a prevalent, preventable pediatric disorder. Identifying genetic risk alleles for FASD is challenging since time, dose, and frequency of exposure are often unknown, and manifestations of FASD are diverse and e...

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Autores principales: Morozova, Tatiana V., Shankar, Vijay, MacPherson, Rebecca A., Mackay, Trudy F. C., Anholt, Robert R. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074282/
https://www.ncbi.nlm.nih.gov/pubmed/35524193
http://dx.doi.org/10.1186/s12864-022-08559-9
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author Morozova, Tatiana V.
Shankar, Vijay
MacPherson, Rebecca A.
Mackay, Trudy F. C.
Anholt, Robert R. H.
author_facet Morozova, Tatiana V.
Shankar, Vijay
MacPherson, Rebecca A.
Mackay, Trudy F. C.
Anholt, Robert R. H.
author_sort Morozova, Tatiana V.
collection PubMed
description BACKGROUND: Prenatal exposure to ethanol can cause fetal alcohol spectrum disorder (FASD), a prevalent, preventable pediatric disorder. Identifying genetic risk alleles for FASD is challenging since time, dose, and frequency of exposure are often unknown, and manifestations of FASD are diverse and evident long after exposure. Drosophila melanogaster is an excellent model to study the genetic basis of the effects of developmental alcohol exposure since many individuals of the same genotype can be reared under controlled environmental conditions. RESULTS: We used 96 sequenced, wild-derived inbred lines from the Drosophila melanogaster Genetic Reference Panel (DGRP) to profile genome-wide transcript abundances in young adult flies that developed on ethanol-supplemented medium or standard culture medium. We found substantial genetic variation in gene expression in response to ethanol with extensive sexual dimorphism. We constructed sex-specific genetic networks associated with alcohol-dependent modulation of gene expression that include protein-coding genes, Novel Transcribed Regions (NTRs, postulated to encode long non-coding RNAs) and female-specific coordinated regulation of snoRNAs that regulate pseudouridylation of ribosomal RNA. We reared DGRP lines which showed extreme upregulation or downregulation of snoRNA expression during developmental alcohol exposure on standard or ethanol supplemented medium and demonstrated that developmental exposure to ethanol has genotype-specific effects on adult locomotor activity and sleep. CONCLUSIONS: There is significant and sex-specific natural genetic variation in the transcriptional response to developmental exposure to ethanol in Drosophila that comprises networks of genes affecting nervous system development and ethanol metabolism as well as networks of regulatory non-coding RNAs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08559-9.
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spelling pubmed-90742822022-05-07 Modulation of the Drosophila transcriptome by developmental exposure to alcohol Morozova, Tatiana V. Shankar, Vijay MacPherson, Rebecca A. Mackay, Trudy F. C. Anholt, Robert R. H. BMC Genomics Research Article BACKGROUND: Prenatal exposure to ethanol can cause fetal alcohol spectrum disorder (FASD), a prevalent, preventable pediatric disorder. Identifying genetic risk alleles for FASD is challenging since time, dose, and frequency of exposure are often unknown, and manifestations of FASD are diverse and evident long after exposure. Drosophila melanogaster is an excellent model to study the genetic basis of the effects of developmental alcohol exposure since many individuals of the same genotype can be reared under controlled environmental conditions. RESULTS: We used 96 sequenced, wild-derived inbred lines from the Drosophila melanogaster Genetic Reference Panel (DGRP) to profile genome-wide transcript abundances in young adult flies that developed on ethanol-supplemented medium or standard culture medium. We found substantial genetic variation in gene expression in response to ethanol with extensive sexual dimorphism. We constructed sex-specific genetic networks associated with alcohol-dependent modulation of gene expression that include protein-coding genes, Novel Transcribed Regions (NTRs, postulated to encode long non-coding RNAs) and female-specific coordinated regulation of snoRNAs that regulate pseudouridylation of ribosomal RNA. We reared DGRP lines which showed extreme upregulation or downregulation of snoRNA expression during developmental alcohol exposure on standard or ethanol supplemented medium and demonstrated that developmental exposure to ethanol has genotype-specific effects on adult locomotor activity and sleep. CONCLUSIONS: There is significant and sex-specific natural genetic variation in the transcriptional response to developmental exposure to ethanol in Drosophila that comprises networks of genes affecting nervous system development and ethanol metabolism as well as networks of regulatory non-coding RNAs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08559-9. BioMed Central 2022-05-06 /pmc/articles/PMC9074282/ /pubmed/35524193 http://dx.doi.org/10.1186/s12864-022-08559-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Morozova, Tatiana V.
Shankar, Vijay
MacPherson, Rebecca A.
Mackay, Trudy F. C.
Anholt, Robert R. H.
Modulation of the Drosophila transcriptome by developmental exposure to alcohol
title Modulation of the Drosophila transcriptome by developmental exposure to alcohol
title_full Modulation of the Drosophila transcriptome by developmental exposure to alcohol
title_fullStr Modulation of the Drosophila transcriptome by developmental exposure to alcohol
title_full_unstemmed Modulation of the Drosophila transcriptome by developmental exposure to alcohol
title_short Modulation of the Drosophila transcriptome by developmental exposure to alcohol
title_sort modulation of the drosophila transcriptome by developmental exposure to alcohol
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074282/
https://www.ncbi.nlm.nih.gov/pubmed/35524193
http://dx.doi.org/10.1186/s12864-022-08559-9
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