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Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries
Single-gene deletions can affect the expression levels of other genes in the same operon in bacterial genomes. Here, we used proteomics for 133 Escherichia coli gene deletion mutants and transcriptome sequencing (RNA-seq) data from 71 mutants to probe the extent of transcriptional and post-transcrip...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547470/ https://www.ncbi.nlm.nih.gov/pubmed/34491080 http://dx.doi.org/10.1128/mSystems.00813-21 |
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author | Mateus, André Shah, Malay Hevler, Johannes Kurzawa, Nils Bobonis, Jacob Typas, Athanasios Savitski, Mikhail M. |
author_facet | Mateus, André Shah, Malay Hevler, Johannes Kurzawa, Nils Bobonis, Jacob Typas, Athanasios Savitski, Mikhail M. |
author_sort | Mateus, André |
collection | PubMed |
description | Single-gene deletions can affect the expression levels of other genes in the same operon in bacterial genomes. Here, we used proteomics for 133 Escherichia coli gene deletion mutants and transcriptome sequencing (RNA-seq) data from 71 mutants to probe the extent of transcriptional and post-transcriptional effects of gene deletions in operons. Transcriptional effects were common on genes located downstream of the deletion and were consistent across all operon members, with nearly 40% of operons showing greater than 2-fold up- or downregulation. Surprisingly, we observed an additional post-transcriptional effect that leads to the downregulation of the gene located directly downstream of the targeted gene. This effect was correlated with their intergenic distance, despite the ribosome binding site of the gene downstream remaining intact during library construction. Overall, the data presented can guide future library construction and highlight the importance of follow-up experiments for assessing direct effects of single-gene deletions in operons. IMPORTANCE Single-gene deletion libraries have allowed genome-wide characterization of gene function and interactions. While each mutant intends to disrupt the function of a single gene, it can unintentionally target other genes, such as those located in the same operon as the deletion. The extent to which such polar effects occur in deletion libraries has not been assessed. In this work, we use proteomics and transcriptomics data to show that transcript level changes lead to nearly 40% of deletions in operons affecting the protein levels of genes located downstream by at least 2-fold. Furthermore, we observed a post-transcriptional effect on the gene located directly downstream of the deletion. These results can guide the design of future gene deletion libraries and emphasizes the importance of follow-up work when linking genotypes to phenotypes. |
format | Online Article Text |
id | pubmed-8547470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85474702021-10-27 Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries Mateus, André Shah, Malay Hevler, Johannes Kurzawa, Nils Bobonis, Jacob Typas, Athanasios Savitski, Mikhail M. mSystems Observation Single-gene deletions can affect the expression levels of other genes in the same operon in bacterial genomes. Here, we used proteomics for 133 Escherichia coli gene deletion mutants and transcriptome sequencing (RNA-seq) data from 71 mutants to probe the extent of transcriptional and post-transcriptional effects of gene deletions in operons. Transcriptional effects were common on genes located downstream of the deletion and were consistent across all operon members, with nearly 40% of operons showing greater than 2-fold up- or downregulation. Surprisingly, we observed an additional post-transcriptional effect that leads to the downregulation of the gene located directly downstream of the targeted gene. This effect was correlated with their intergenic distance, despite the ribosome binding site of the gene downstream remaining intact during library construction. Overall, the data presented can guide future library construction and highlight the importance of follow-up experiments for assessing direct effects of single-gene deletions in operons. IMPORTANCE Single-gene deletion libraries have allowed genome-wide characterization of gene function and interactions. While each mutant intends to disrupt the function of a single gene, it can unintentionally target other genes, such as those located in the same operon as the deletion. The extent to which such polar effects occur in deletion libraries has not been assessed. In this work, we use proteomics and transcriptomics data to show that transcript level changes lead to nearly 40% of deletions in operons affecting the protein levels of genes located downstream by at least 2-fold. Furthermore, we observed a post-transcriptional effect on the gene located directly downstream of the deletion. These results can guide the design of future gene deletion libraries and emphasizes the importance of follow-up work when linking genotypes to phenotypes. American Society for Microbiology 2021-09-07 /pmc/articles/PMC8547470/ /pubmed/34491080 http://dx.doi.org/10.1128/mSystems.00813-21 Text en Copyright © 2021 Mateus et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Observation Mateus, André Shah, Malay Hevler, Johannes Kurzawa, Nils Bobonis, Jacob Typas, Athanasios Savitski, Mikhail M. Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries |
title | Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries |
title_full | Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries |
title_fullStr | Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries |
title_full_unstemmed | Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries |
title_short | Transcriptional and Post-Transcriptional Polar Effects in Bacterial Gene Deletion Libraries |
title_sort | transcriptional and post-transcriptional polar effects in bacterial gene deletion libraries |
topic | Observation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547470/ https://www.ncbi.nlm.nih.gov/pubmed/34491080 http://dx.doi.org/10.1128/mSystems.00813-21 |
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