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Effects of FUdR on gene expression in the C. elegans bacterial diet OP50
OBJECTIVE: Many C. elegans aging studies use the compound 5-fluro-2ʹ-deoxyuridine (FUdR) to produce a synchronous population of worms. However, the effects of FUdR on the bacterial gene expression of OP50 E. coli, the primary laboratory C. elegans food source, is not fully understood. This is partic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186096/ https://www.ncbi.nlm.nih.gov/pubmed/34103088 http://dx.doi.org/10.1186/s13104-021-05624-6 |
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author | McIntyre, Grace Wright, Justin Wong, Hoi Tong Lamendella, Regina Chan, Jason |
author_facet | McIntyre, Grace Wright, Justin Wong, Hoi Tong Lamendella, Regina Chan, Jason |
author_sort | McIntyre, Grace |
collection | PubMed |
description | OBJECTIVE: Many C. elegans aging studies use the compound 5-fluro-2ʹ-deoxyuridine (FUdR) to produce a synchronous population of worms. However, the effects of FUdR on the bacterial gene expression of OP50 E. coli, the primary laboratory C. elegans food source, is not fully understood. This is particularly relevant as studies suggest that intestinal microbes can affect C. elegans physiology. Therefore, it is imperative that we understand how exposure to FUdR can affect gene expression changes in OP50 E. coli. RESULTS: An RNAseq dataset comprised of expression patterns of 2900 E. coli genes in the strain OP50, which were seeded on either nematode growth media (NGM) plates or on FUdR (50 µM) supplemented NGM plates, was analyzed. Analysis showed differential gene expression in genes involved in general transport, amino acid biosynthesis, transcription, iron transport, and antibiotic resistance. We specifically highlight metabolic enzymes in the l-histidine biosynthesis pathway as differentially expressed between NGM and FUdR exposed OP50. We conclude that OP50 exposed to FUdR results in differential expression of many genes, including those in amino acid biosynthetic pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-021-05624-6. |
format | Online Article Text |
id | pubmed-8186096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81860962021-06-10 Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 McIntyre, Grace Wright, Justin Wong, Hoi Tong Lamendella, Regina Chan, Jason BMC Res Notes Research Note OBJECTIVE: Many C. elegans aging studies use the compound 5-fluro-2ʹ-deoxyuridine (FUdR) to produce a synchronous population of worms. However, the effects of FUdR on the bacterial gene expression of OP50 E. coli, the primary laboratory C. elegans food source, is not fully understood. This is particularly relevant as studies suggest that intestinal microbes can affect C. elegans physiology. Therefore, it is imperative that we understand how exposure to FUdR can affect gene expression changes in OP50 E. coli. RESULTS: An RNAseq dataset comprised of expression patterns of 2900 E. coli genes in the strain OP50, which were seeded on either nematode growth media (NGM) plates or on FUdR (50 µM) supplemented NGM plates, was analyzed. Analysis showed differential gene expression in genes involved in general transport, amino acid biosynthesis, transcription, iron transport, and antibiotic resistance. We specifically highlight metabolic enzymes in the l-histidine biosynthesis pathway as differentially expressed between NGM and FUdR exposed OP50. We conclude that OP50 exposed to FUdR results in differential expression of many genes, including those in amino acid biosynthetic pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-021-05624-6. BioMed Central 2021-05-28 /pmc/articles/PMC8186096/ /pubmed/34103088 http://dx.doi.org/10.1186/s13104-021-05624-6 Text en © The Author(s) 2021 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 Note McIntyre, Grace Wright, Justin Wong, Hoi Tong Lamendella, Regina Chan, Jason Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 |
title | Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 |
title_full | Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 |
title_fullStr | Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 |
title_full_unstemmed | Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 |
title_short | Effects of FUdR on gene expression in the C. elegans bacterial diet OP50 |
title_sort | effects of fudr on gene expression in the c. elegans bacterial diet op50 |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186096/ https://www.ncbi.nlm.nih.gov/pubmed/34103088 http://dx.doi.org/10.1186/s13104-021-05624-6 |
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