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Driving the expression of the Salmonella enterica sv Typhimurium flagellum using flhDC from Escherichia coli results in key regulatory and cellular differences
The flagellar systems of Escherichia coli and Salmonella enterica exhibit a significant level of genetic and functional synteny. Both systems are controlled by the flagellar specific master regulator FlhD 4 C 2 . Since the early days of genetic analyses of flagellar systems it has been known that E....
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Published in: | Scientific reports 2018-11, Vol.8 (1), p.16705-11, Article 16705 |
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description | The flagellar systems of
Escherichia coli
and
Salmonella enterica
exhibit a significant level of genetic and functional synteny. Both systems are controlled by the flagellar specific master regulator FlhD
4
C
2
. Since the early days of genetic analyses of flagellar systems it has been known that
E. coli flhDC
can complement a ∆
flhDC
mutant in
S. enterica
. The genomic revolution has identified how genetic changes to transcription factors and/or DNA binding sites can impact the phenotypic outcome across related species. We were therefore interested in asking: using modern tools to interrogate flagellar gene expression and assembly, what would the impact be of replacing the
flhDC
coding sequences in
S. enterica
for the
E. coli
genes at the
flhDC S. entercia
chromosomal locus? We show that even though all strains created are motile, flagellar gene expression is measurably lower when
flhDC
EC
are present. These changes can be attributed to the impact of FlhD
4
C
2
DNA recognition and the protein-protein interactions required to generate a stable FlhD
4
C
2
complex. Furthermore, our data suggests that in
E. coli
the internal flagellar FliT regulatory feedback loop has a marked difference with respect to output of the flagellar systems. We argue due diligence is required in making assumptions based on heterologous expression of regulators and that even systems showing significant synteny may not behave in exactly the same manner. |
doi_str_mv | 10.1038/s41598-018-35005-2 |
format | article |
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Escherichia coli
and
Salmonella enterica
exhibit a significant level of genetic and functional synteny. Both systems are controlled by the flagellar specific master regulator FlhD
4
C
2
. Since the early days of genetic analyses of flagellar systems it has been known that
E. coli flhDC
can complement a ∆
flhDC
mutant in
S. enterica
. The genomic revolution has identified how genetic changes to transcription factors and/or DNA binding sites can impact the phenotypic outcome across related species. We were therefore interested in asking: using modern tools to interrogate flagellar gene expression and assembly, what would the impact be of replacing the
flhDC
coding sequences in
S. enterica
for the
E. coli
genes at the
flhDC S. entercia
chromosomal locus? We show that even though all strains created are motile, flagellar gene expression is measurably lower when
flhDC
EC
are present. These changes can be attributed to the impact of FlhD
4
C
2
DNA recognition and the protein-protein interactions required to generate a stable FlhD
4
C
2
complex. Furthermore, our data suggests that in
E. coli
the internal flagellar FliT regulatory feedback loop has a marked difference with respect to output of the flagellar systems. We argue due diligence is required in making assumptions based on heterologous expression of regulators and that even systems showing significant synteny may not behave in exactly the same manner.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-35005-2</identifier><identifier>PMID: 30420601</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14/35 ; 14/63 ; 38/5 ; 38/70 ; 42/41 ; 631/326/1320 ; 631/326/325/1506 ; Binding sites ; Deoxyribonucleic acid ; DNA ; E coli ; Escherichia coli ; Flagella ; Gene expression ; Genetic analysis ; Humanities and Social Sciences ; multidisciplinary ; Protein interaction ; Salmonella ; Salmonella enterica ; Science ; Science (multidisciplinary) ; Synteny ; Transcription factors</subject><ispartof>Scientific reports, 2018-11, Vol.8 (1), p.16705-11, Article 16705</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-bf94956e62f91b11b1ae2bf984f47e5b8cf43999f6909f8295f3db6eb79f811d3</citedby><cites>FETCH-LOGICAL-c511t-bf94956e62f91b11b1ae2bf984f47e5b8cf43999f6909f8295f3db6eb79f811d3</cites><orcidid>0000-0003-4332-1640 ; 0000-0001-6488-7593</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2132250739/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2132250739?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,37011,44588,53789,53791,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30420601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albanna, Ayman</creatorcontrib><creatorcontrib>Sim, Martin</creatorcontrib><creatorcontrib>Hoskisson, Paul A.</creatorcontrib><creatorcontrib>Gillespie, Colin</creatorcontrib><creatorcontrib>Rao, Christopher V.</creatorcontrib><creatorcontrib>Aldridge, Phillip D.</creatorcontrib><title>Driving the expression of the Salmonella enterica sv Typhimurium flagellum using flhDC from Escherichia coli results in key regulatory and cellular differences</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The flagellar systems of
Escherichia coli
and
Salmonella enterica
exhibit a significant level of genetic and functional synteny. Both systems are controlled by the flagellar specific master regulator FlhD
4
C
2
. Since the early days of genetic analyses of flagellar systems it has been known that
E. coli flhDC
can complement a ∆
flhDC
mutant in
S. enterica
. The genomic revolution has identified how genetic changes to transcription factors and/or DNA binding sites can impact the phenotypic outcome across related species. We were therefore interested in asking: using modern tools to interrogate flagellar gene expression and assembly, what would the impact be of replacing the
flhDC
coding sequences in
S. enterica
for the
E. coli
genes at the
flhDC S. entercia
chromosomal locus? We show that even though all strains created are motile, flagellar gene expression is measurably lower when
flhDC
EC
are present. These changes can be attributed to the impact of FlhD
4
C
2
DNA recognition and the protein-protein interactions required to generate a stable FlhD
4
C
2
complex. Furthermore, our data suggests that in
E. coli
the internal flagellar FliT regulatory feedback loop has a marked difference with respect to output of the flagellar systems. We argue due diligence is required in making assumptions based on heterologous expression of regulators and that even systems showing significant synteny may not behave in exactly the same manner.</description><subject>14/35</subject><subject>14/63</subject><subject>38/5</subject><subject>38/70</subject><subject>42/41</subject><subject>631/326/1320</subject><subject>631/326/325/1506</subject><subject>Binding sites</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Flagella</subject><subject>Gene expression</subject><subject>Genetic analysis</subject><subject>Humanities and Social Sciences</subject><subject>multidisciplinary</subject><subject>Protein interaction</subject><subject>Salmonella</subject><subject>Salmonella enterica</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Synteny</subject><subject>Transcription factors</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9Uk1v1DAQjRCIVqV_gAOyxIVLij_ibHxBQttSkCpxoJwtJxlvXBx7sZMV-2v4q0x2SykcsCx5Zvzm2c9-RfGS0QtGRfM2V0yqpqSsKYWkVJb8SXHKaYWB4Pzpo_ikOM_5juKQXFVMPS9OBK04rSk7LX5eJrdzYUOmAQj82CbI2cVAoj1Uvhg_xgDeGwJhguQ6Q_KO3O63gxvn5OaRWG82CMBozguR9cPlmtgUR3KVu2HpGZwhXfSOIPvsp0xcIN9gj-lm9maKaU9M6Em30HiTSO-shQShg_yieGaNz3B-v54VXz9c3a4_ljefrz-t39-UnWRsKlurKiVrqLlVrGU4DXAsNpWtViDbprOVUErZWlFlG66kFX1bQ7vCjLFenBXvjrzbuR2h71BtMl5vkxtN2utonP57J7hBb-JO1_jEjDVI8OaeIMXvM-RJjy4vikyAOGfNmeArIZtGIvT1P9C7OKeA8g4oLulKKETxI6pLMecE9uEyjOrFAvpoAY0W0AcLaI5Nrx7LeGj5_eEIEEdAxq2wgfTn7P_Q_gIm7cBQ</recordid><startdate>20181112</startdate><enddate>20181112</enddate><creator>Albanna, Ayman</creator><creator>Sim, Martin</creator><creator>Hoskisson, Paul A.</creator><creator>Gillespie, Colin</creator><creator>Rao, Christopher V.</creator><creator>Aldridge, Phillip D.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4332-1640</orcidid><orcidid>https://orcid.org/0000-0001-6488-7593</orcidid></search><sort><creationdate>20181112</creationdate><title>Driving the expression of the Salmonella enterica sv Typhimurium flagellum using flhDC from Escherichia coli results in key regulatory and cellular differences</title><author>Albanna, Ayman ; 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Escherichia coli
and
Salmonella enterica
exhibit a significant level of genetic and functional synteny. Both systems are controlled by the flagellar specific master regulator FlhD
4
C
2
. Since the early days of genetic analyses of flagellar systems it has been known that
E. coli flhDC
can complement a ∆
flhDC
mutant in
S. enterica
. The genomic revolution has identified how genetic changes to transcription factors and/or DNA binding sites can impact the phenotypic outcome across related species. We were therefore interested in asking: using modern tools to interrogate flagellar gene expression and assembly, what would the impact be of replacing the
flhDC
coding sequences in
S. enterica
for the
E. coli
genes at the
flhDC S. entercia
chromosomal locus? We show that even though all strains created are motile, flagellar gene expression is measurably lower when
flhDC
EC
are present. These changes can be attributed to the impact of FlhD
4
C
2
DNA recognition and the protein-protein interactions required to generate a stable FlhD
4
C
2
complex. Furthermore, our data suggests that in
E. coli
the internal flagellar FliT regulatory feedback loop has a marked difference with respect to output of the flagellar systems. We argue due diligence is required in making assumptions based on heterologous expression of regulators and that even systems showing significant synteny may not behave in exactly the same manner.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30420601</pmid><doi>10.1038/s41598-018-35005-2</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4332-1640</orcidid><orcidid>https://orcid.org/0000-0001-6488-7593</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 14/35 14/63 38/5 38/70 42/41 631/326/1320 631/326/325/1506 Binding sites Deoxyribonucleic acid DNA E coli Escherichia coli Flagella Gene expression Genetic analysis Humanities and Social Sciences multidisciplinary Protein interaction Salmonella Salmonella enterica Science Science (multidisciplinary) Synteny Transcription factors |
title | Driving the expression of the Salmonella enterica sv Typhimurium flagellum using flhDC from Escherichia coli results in key regulatory and cellular differences |
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