Cargando…
The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization
BACKGROUND: One of the most complex prokaryotic organelles are magnetosomes, which are formed by magnetotactic bacteria as sensors for navigation in the Earth’s magnetic field. In the alphaproteobacterium Magnetospirillum gryphiswaldense magnetosomes consist of chains of magnetite crystals (Fe(3)O(4...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549626/ https://www.ncbi.nlm.nih.gov/pubmed/36217140 http://dx.doi.org/10.1186/s12864-022-08913-x |
_version_ | 1784805714182537216 |
---|---|
author | Riese, Cornelius N. Wittchen, Manuel Jérôme, Valérie Freitag, Ruth Busche, Tobias Kalinowski, Jörn Schüler, Dirk |
author_facet | Riese, Cornelius N. Wittchen, Manuel Jérôme, Valérie Freitag, Ruth Busche, Tobias Kalinowski, Jörn Schüler, Dirk |
author_sort | Riese, Cornelius N. |
collection | PubMed |
description | BACKGROUND: One of the most complex prokaryotic organelles are magnetosomes, which are formed by magnetotactic bacteria as sensors for navigation in the Earth’s magnetic field. In the alphaproteobacterium Magnetospirillum gryphiswaldense magnetosomes consist of chains of magnetite crystals (Fe(3)O(4)) that under microoxic to anoxic conditions are biomineralized within membrane vesicles. To form such an intricate structure, the transcription of > 30 specific structural genes clustered within the genomic magnetosome island (MAI) has to be coordinated with the expression of an as-yet unknown number of auxiliary genes encoding several generic metabolic functions. However, their global regulation and transcriptional organization in response to anoxic conditions most favorable for magnetite biomineralization are still unclear. RESULTS: Here, we compared transcriptional profiles of anaerobically grown magnetosome forming cells with those in which magnetosome biosynthesis has been suppressed by aerobic condition. Using whole transcriptome shotgun sequencing, we found that transcription of about 300 of the > 4300 genes was significantly enhanced during magnetosome formation. About 40 of the top upregulated genes are directly or indirectly linked to aerobic and anaerobic respiration (denitrification) or unknown functions. The mam and mms gene clusters, specifically controlling magnetosome biosynthesis, were highly transcribed, but constitutively expressed irrespective of the growth condition. By Cappable-sequencing, we show that the transcriptional complexity of both the MAI and the entire genome decreased under anaerobic conditions optimal for magnetosome formation. In addition, predominant promoter structures were highly similar to sigma factor σ(70) dependent promoters in other Alphaproteobacteria. CONCLUSIONS: Our transcriptome-wide analysis revealed that magnetite biomineralization relies on a complex interplay between generic metabolic processes such as aerobic and anaerobic respiration, cellular redox control, and the biosynthesis of specific magnetosome structures. In addition, we provide insights into global regulatory features that have remained uncharacterized in the widely studied model organism M. gryphiswaldense, including a comprehensive dataset of newly annotated transcription start sites and genome-wide operon detection as a community resource (GEO Series accession number GSE197098). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08913-x. |
format | Online Article Text |
id | pubmed-9549626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95496262022-10-11 The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization Riese, Cornelius N. Wittchen, Manuel Jérôme, Valérie Freitag, Ruth Busche, Tobias Kalinowski, Jörn Schüler, Dirk BMC Genomics Research BACKGROUND: One of the most complex prokaryotic organelles are magnetosomes, which are formed by magnetotactic bacteria as sensors for navigation in the Earth’s magnetic field. In the alphaproteobacterium Magnetospirillum gryphiswaldense magnetosomes consist of chains of magnetite crystals (Fe(3)O(4)) that under microoxic to anoxic conditions are biomineralized within membrane vesicles. To form such an intricate structure, the transcription of > 30 specific structural genes clustered within the genomic magnetosome island (MAI) has to be coordinated with the expression of an as-yet unknown number of auxiliary genes encoding several generic metabolic functions. However, their global regulation and transcriptional organization in response to anoxic conditions most favorable for magnetite biomineralization are still unclear. RESULTS: Here, we compared transcriptional profiles of anaerobically grown magnetosome forming cells with those in which magnetosome biosynthesis has been suppressed by aerobic condition. Using whole transcriptome shotgun sequencing, we found that transcription of about 300 of the > 4300 genes was significantly enhanced during magnetosome formation. About 40 of the top upregulated genes are directly or indirectly linked to aerobic and anaerobic respiration (denitrification) or unknown functions. The mam and mms gene clusters, specifically controlling magnetosome biosynthesis, were highly transcribed, but constitutively expressed irrespective of the growth condition. By Cappable-sequencing, we show that the transcriptional complexity of both the MAI and the entire genome decreased under anaerobic conditions optimal for magnetosome formation. In addition, predominant promoter structures were highly similar to sigma factor σ(70) dependent promoters in other Alphaproteobacteria. CONCLUSIONS: Our transcriptome-wide analysis revealed that magnetite biomineralization relies on a complex interplay between generic metabolic processes such as aerobic and anaerobic respiration, cellular redox control, and the biosynthesis of specific magnetosome structures. In addition, we provide insights into global regulatory features that have remained uncharacterized in the widely studied model organism M. gryphiswaldense, including a comprehensive dataset of newly annotated transcription start sites and genome-wide operon detection as a community resource (GEO Series accession number GSE197098). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08913-x. BioMed Central 2022-10-10 /pmc/articles/PMC9549626/ /pubmed/36217140 http://dx.doi.org/10.1186/s12864-022-08913-x 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 Riese, Cornelius N. Wittchen, Manuel Jérôme, Valérie Freitag, Ruth Busche, Tobias Kalinowski, Jörn Schüler, Dirk The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization |
title | The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization |
title_full | The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization |
title_fullStr | The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization |
title_full_unstemmed | The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization |
title_short | The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization |
title_sort | transcriptomic landscape of magnetospirillum gryphiswaldense during magnetosome biomineralization |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549626/ https://www.ncbi.nlm.nih.gov/pubmed/36217140 http://dx.doi.org/10.1186/s12864-022-08913-x |
work_keys_str_mv | AT riesecorneliusn thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT wittchenmanuel thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT jeromevalerie thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT freitagruth thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT buschetobias thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT kalinowskijorn thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT schulerdirk thetranscriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT riesecorneliusn transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT wittchenmanuel transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT jeromevalerie transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT freitagruth transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT buschetobias transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT kalinowskijorn transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization AT schulerdirk transcriptomiclandscapeofmagnetospirillumgryphiswaldenseduringmagnetosomebiomineralization |