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Genome-Wide TSS Distribution in Three Related Clostridia with Normalized Capp-Switch Sequencing
Transcription initiation is a tightly regulated process that is crucial for many aspects of prokaryotic physiology. High-throughput transcription start site (TSS) mapping can shed light on global and local regulation of transcription initiation, which in turn may help us understand and predict micro...
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Published in: | Microbiology spectrum 2022-04, Vol.10 (2), p.e0228821-e0228821 |
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description | Transcription initiation is a tightly regulated process that is crucial for many aspects of prokaryotic physiology. High-throughput transcription start site (TSS) mapping can shed light on global and local regulation of transcription initiation, which in turn may help us understand and predict microbial behavior. In this study, we used Capp-Switch sequencing to determine the TSS positions in the genomes of three model solventogenic clostridia: Clostridium acetobutylicum ATCC 824, C. beijerinckii DSM 6423, and C. beijerinckii NCIMB 8052. We first refined the approach by implementing a normalization pipeline accounting for gene expression, yielding a total of 12,114 mapped TSSs across the species. We further compared the distributions of these sites in the three strains. Results indicated similar distribution patterns at the genome scale, but also some sharp differences, such as for the butyryl-CoA synthesis operon, particularly when comparing C. acetobutylicum to the C. beijerinckii strains. Lastly, we found that promoter structure is generally poorly conserved between C. acetobutylicum and C. beijerinckii. A few conserved promoters across species are discussed, showing interesting examples of how TSS determination and comparison can improve our understanding of gene expression regulation at the transcript level.
Solventogenic clostridia have been employed in industry for more than a century, initially being used in the acetone-butanol-ethanol (ABE) fermentation process for acetone and butanol production. Interest in these bacteria has recently increased in the context of green chemistry and sustainable development. However, our current understanding of their genomes and physiology limits their optimal use as industrial solvent production platforms. The gene regulatory mechanisms of solventogenesis are still only partly understood, impeding efforts to increase rates and yields. Genome-wide mapping of transcription start sites (TSSs) for three model solventogenic
strains is an important step toward understanding mechanisms of gene regulation in these industrially important bacteria. |
doi_str_mv | 10.1128/spectrum.02288-21 |
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Solventogenic clostridia have been employed in industry for more than a century, initially being used in the acetone-butanol-ethanol (ABE) fermentation process for acetone and butanol production. Interest in these bacteria has recently increased in the context of green chemistry and sustainable development. However, our current understanding of their genomes and physiology limits their optimal use as industrial solvent production platforms. The gene regulatory mechanisms of solventogenesis are still only partly understood, impeding efforts to increase rates and yields. Genome-wide mapping of transcription start sites (TSSs) for three model solventogenic
strains is an important step toward understanding mechanisms of gene regulation in these industrially important bacteria.</description><identifier>ISSN: 2165-0497</identifier><identifier>EISSN: 2165-0497</identifier><identifier>DOI: 10.1128/spectrum.02288-21</identifier><identifier>PMID: 35412381</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Acetone - metabolism ; Applied and Industrial Microbiology ; Bacteria, Anaerobic ; butanol ; Butanols - metabolism ; Clostridium ; Clostridium - genetics ; Clostridium - metabolism ; Clostridium acetobutylicum - genetics ; Clostridium acetobutylicum - metabolism ; Fermentation ; Life Sciences ; Research Article ; solvents ; transcriptional regulation</subject><ispartof>Microbiology spectrum, 2022-04, Vol.10 (2), p.e0228821-e0228821</ispartof><rights>Copyright © 2022 Hocq et al.</rights><rights>Attribution</rights><rights>Copyright © 2022 Hocq et al. 2022 Hocq et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a538t-c804bfae4ee19db270be82241c3dc6a15422b762ad7dafd342c231f379d959f23</citedby><cites>FETCH-LOGICAL-a538t-c804bfae4ee19db270be82241c3dc6a15422b762ad7dafd342c231f379d959f23</cites><orcidid>0000-0001-5907-4504 ; 0000-0002-4641-0270</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/spectrum.02288-21$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/spectrum.02288-21$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27900,27901,52725,52726,52727,53765,53767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35412381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://ifp.hal.science/hal-03706159$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Auchtung, Jennifer M</contributor><creatorcontrib>Hocq, Rémi</creatorcontrib><creatorcontrib>Jagtap, Surabhi</creatorcontrib><creatorcontrib>Boutard, Magali</creatorcontrib><creatorcontrib>Tolonen, Andrew C</creatorcontrib><creatorcontrib>Duval, Laurent</creatorcontrib><creatorcontrib>Pirayre, Aurélie</creatorcontrib><creatorcontrib>Lopes Ferreira, Nicolas</creatorcontrib><creatorcontrib>Wasels, François</creatorcontrib><title>Genome-Wide TSS Distribution in Three Related Clostridia with Normalized Capp-Switch Sequencing</title><title>Microbiology spectrum</title><addtitle>Microbiol Spectr</addtitle><addtitle>Microbiol Spectr</addtitle><description>Transcription initiation is a tightly regulated process that is crucial for many aspects of prokaryotic physiology. High-throughput transcription start site (TSS) mapping can shed light on global and local regulation of transcription initiation, which in turn may help us understand and predict microbial behavior. In this study, we used Capp-Switch sequencing to determine the TSS positions in the genomes of three model solventogenic clostridia: Clostridium acetobutylicum ATCC 824, C. beijerinckii DSM 6423, and C. beijerinckii NCIMB 8052. We first refined the approach by implementing a normalization pipeline accounting for gene expression, yielding a total of 12,114 mapped TSSs across the species. We further compared the distributions of these sites in the three strains. Results indicated similar distribution patterns at the genome scale, but also some sharp differences, such as for the butyryl-CoA synthesis operon, particularly when comparing C. acetobutylicum to the C. beijerinckii strains. Lastly, we found that promoter structure is generally poorly conserved between C. acetobutylicum and C. beijerinckii. A few conserved promoters across species are discussed, showing interesting examples of how TSS determination and comparison can improve our understanding of gene expression regulation at the transcript level.
Solventogenic clostridia have been employed in industry for more than a century, initially being used in the acetone-butanol-ethanol (ABE) fermentation process for acetone and butanol production. Interest in these bacteria has recently increased in the context of green chemistry and sustainable development. However, our current understanding of their genomes and physiology limits their optimal use as industrial solvent production platforms. The gene regulatory mechanisms of solventogenesis are still only partly understood, impeding efforts to increase rates and yields. Genome-wide mapping of transcription start sites (TSSs) for three model solventogenic
strains is an important step toward understanding mechanisms of gene regulation in these industrially important bacteria.</description><subject>Acetone - metabolism</subject><subject>Applied and Industrial Microbiology</subject><subject>Bacteria, Anaerobic</subject><subject>butanol</subject><subject>Butanols - metabolism</subject><subject>Clostridium</subject><subject>Clostridium - genetics</subject><subject>Clostridium - metabolism</subject><subject>Clostridium acetobutylicum - genetics</subject><subject>Clostridium acetobutylicum - metabolism</subject><subject>Fermentation</subject><subject>Life Sciences</subject><subject>Research Article</subject><subject>solvents</subject><subject>transcriptional regulation</subject><issn>2165-0497</issn><issn>2165-0497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kkFv1DAQhSMEolXpD-CCcoRDFnscJ84FqVqgrbQCiV3E0ZrYk12vknixkyL49WSbtmo5cLL1Zt43GvslyWvOFpyDeh8PZIYwdgsGoFQG_FlyCryQGcur8vmj-0lyHuOeMcY5kyDhZXIiZM5BKH6a6EvqfUfZD2cp3azX6UcXh-DqcXC-T12fbnaBKP1GLQ5k02Xrj2XrMP3lhl36xYcOW_fnWMLDIVtPqtmla_o5Um9cv32VvGiwjXR-d54l3z9_2iyvstXXy-vlxSpDKdSQGcXyukHKiXhlayhZTQog50ZYUyCXOUBdFoC2tNhYkYMBwRtRVraSVQPiLLmeudbjXh-C6zD81h6dvhV82GoMgzMtaVKyBsZNbkvMJSpFwCWiggJRSGkm1oeZdRjrjqyhfgjYPoE-rfRup7f-Rlcsl6CqCfBuBuz-sV1drPRRY6JkBZfVDZ96394NC356tDjozkVDbYs9-TFqKPJKKlmKYmrlc6sJPsZAzQObM33MhL7PhL7NhIYjfjF7MHag934M_fQN_zW8ebz8w4j7yIi_2DfD-g</recordid><startdate>20220427</startdate><enddate>20220427</enddate><creator>Hocq, Rémi</creator><creator>Jagtap, Surabhi</creator><creator>Boutard, Magali</creator><creator>Tolonen, Andrew C</creator><creator>Duval, Laurent</creator><creator>Pirayre, Aurélie</creator><creator>Lopes Ferreira, Nicolas</creator><creator>Wasels, François</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5907-4504</orcidid><orcidid>https://orcid.org/0000-0002-4641-0270</orcidid></search><sort><creationdate>20220427</creationdate><title>Genome-Wide TSS Distribution in Three Related Clostridia with Normalized Capp-Switch Sequencing</title><author>Hocq, Rémi ; Jagtap, Surabhi ; Boutard, Magali ; Tolonen, Andrew C ; Duval, Laurent ; Pirayre, Aurélie ; Lopes Ferreira, Nicolas ; Wasels, François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a538t-c804bfae4ee19db270be82241c3dc6a15422b762ad7dafd342c231f379d959f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetone - metabolism</topic><topic>Applied and Industrial Microbiology</topic><topic>Bacteria, Anaerobic</topic><topic>butanol</topic><topic>Butanols - metabolism</topic><topic>Clostridium</topic><topic>Clostridium - genetics</topic><topic>Clostridium - metabolism</topic><topic>Clostridium acetobutylicum - genetics</topic><topic>Clostridium acetobutylicum - metabolism</topic><topic>Fermentation</topic><topic>Life Sciences</topic><topic>Research Article</topic><topic>solvents</topic><topic>transcriptional regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hocq, Rémi</creatorcontrib><creatorcontrib>Jagtap, Surabhi</creatorcontrib><creatorcontrib>Boutard, Magali</creatorcontrib><creatorcontrib>Tolonen, Andrew C</creatorcontrib><creatorcontrib>Duval, Laurent</creatorcontrib><creatorcontrib>Pirayre, Aurélie</creatorcontrib><creatorcontrib>Lopes Ferreira, Nicolas</creatorcontrib><creatorcontrib>Wasels, François</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Microbiology spectrum</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hocq, Rémi</au><au>Jagtap, Surabhi</au><au>Boutard, Magali</au><au>Tolonen, Andrew C</au><au>Duval, Laurent</au><au>Pirayre, Aurélie</au><au>Lopes Ferreira, Nicolas</au><au>Wasels, François</au><au>Auchtung, Jennifer M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-Wide TSS Distribution in Three Related Clostridia with Normalized Capp-Switch Sequencing</atitle><jtitle>Microbiology spectrum</jtitle><stitle>Microbiol Spectr</stitle><addtitle>Microbiol Spectr</addtitle><date>2022-04-27</date><risdate>2022</risdate><volume>10</volume><issue>2</issue><spage>e0228821</spage><epage>e0228821</epage><pages>e0228821-e0228821</pages><issn>2165-0497</issn><eissn>2165-0497</eissn><abstract>Transcription initiation is a tightly regulated process that is crucial for many aspects of prokaryotic physiology. High-throughput transcription start site (TSS) mapping can shed light on global and local regulation of transcription initiation, which in turn may help us understand and predict microbial behavior. In this study, we used Capp-Switch sequencing to determine the TSS positions in the genomes of three model solventogenic clostridia: Clostridium acetobutylicum ATCC 824, C. beijerinckii DSM 6423, and C. beijerinckii NCIMB 8052. We first refined the approach by implementing a normalization pipeline accounting for gene expression, yielding a total of 12,114 mapped TSSs across the species. We further compared the distributions of these sites in the three strains. Results indicated similar distribution patterns at the genome scale, but also some sharp differences, such as for the butyryl-CoA synthesis operon, particularly when comparing C. acetobutylicum to the C. beijerinckii strains. Lastly, we found that promoter structure is generally poorly conserved between C. acetobutylicum and C. beijerinckii. A few conserved promoters across species are discussed, showing interesting examples of how TSS determination and comparison can improve our understanding of gene expression regulation at the transcript level.
Solventogenic clostridia have been employed in industry for more than a century, initially being used in the acetone-butanol-ethanol (ABE) fermentation process for acetone and butanol production. Interest in these bacteria has recently increased in the context of green chemistry and sustainable development. However, our current understanding of their genomes and physiology limits their optimal use as industrial solvent production platforms. The gene regulatory mechanisms of solventogenesis are still only partly understood, impeding efforts to increase rates and yields. Genome-wide mapping of transcription start sites (TSSs) for three model solventogenic
strains is an important step toward understanding mechanisms of gene regulation in these industrially important bacteria.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>35412381</pmid><doi>10.1128/spectrum.02288-21</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-5907-4504</orcidid><orcidid>https://orcid.org/0000-0002-4641-0270</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetone - metabolism Applied and Industrial Microbiology Bacteria, Anaerobic butanol Butanols - metabolism Clostridium Clostridium - genetics Clostridium - metabolism Clostridium acetobutylicum - genetics Clostridium acetobutylicum - metabolism Fermentation Life Sciences Research Article solvents transcriptional regulation |
title | Genome-Wide TSS Distribution in Three Related Clostridia with Normalized Capp-Switch Sequencing |
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