Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mateus, André, Shah, Malay, Hevler, Johannes, Kurzawa, Nils, Bobonis, Jacob, Typas, Athanasios, Savitski, Mikhail M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
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
_version_ 1784590386979667968
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
work_keys_str_mv AT mateusandre transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries
AT shahmalay transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries
AT hevlerjohannes transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries
AT kurzawanils transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries
AT bobonisjacob transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries
AT typasathanasios transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries
AT savitskimikhailm transcriptionalandposttranscriptionalpolareffectsinbacterialgenedeletionlibraries