{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/29559"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/29559","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Regulation of the Mannose PTS Operon by the small RNA SgrS","abstract":"A number of bacterial small RNAs (sRNAs) act as global regulators of stress responses by controlling expression of multiple genes. The sRNA SgrS is expressed in response to glucose-phosphate stress, a condition associated with disruption of glycolytic flux and accumulation of sugar-phosphates. SgrS has been shown to stimulate degradation of the ptsG mRNA, encoding the major glucose transporter. This study demonstrates that SgrS regulates the genes encoding the mannose and secondary glucose transporter, manXYZ. Analysis of manXYZ mRNA stability and translation in the presence and absence of SgrS indicate that manXYZ is regulated by SgrS under stress conditions and when SgrS is ectopically expressed. In vitro footprinting and in vivo mutational analyses showed that SgrS base pairs with manXYZ within the manX coding sequence to prevent manX translation. Regulation of manX did not require the RNase E degradosome complex, suggesting that the primary mechanism of regulation is translational. An Escherichia coli ptsG mutant strain that is manXYZ(+) experiences stress when exposed to the glucose analogs α- methyl glucoside or 2-deoxyglucose. A ptsG manXYZ double mutant is resistant to the stress, indicating that PTS transporters encoded by both SgrS targets are involved in taking up substrates that cause stress. We further demonstrate that SgrS binds to two sites on the manXYZ mRNA to coordinately down-regulate translation of all the cistrons, a mechanism reminiscent of that used by the eukaryotic miRNA, lin-4 for regulation of the lin-14 mRNA. We tested the hypothesis that regulation of manY and manZ is dependent on SgrS:manX base pairing and subsequent manXYZ mRNA degradation. Contrary to the hypothesis, we show that SgrS repression of iii manY and manZ translation can be decoupled from SgrS-dependent manXYZ mRNA degradation. Furthermore, SgrS regulates manY translation by a mechanism that is independent of SgrS:manX mRNA interactions. Instead, translational regulation of manY depends on SgrS pairing with sequences in the manX-manY intergenic region, upstream of the manY ribosome binding site. Mutational analysis suggests that while the SgrS-manY interaction is sufficient to stimulate some degradation of the manXYZ mRNA, pairing with both sites is required for maximal degradation of the manXYZ mRNA. Additional SgrS candidate-mRNA targets are also investigated.","abstract_html":"A number of bacterial small RNAs (sRNAs) act as global regulators of stress responses by controlling expression of multiple genes. The sRNA SgrS is expressed in response to glucose-phosphate stress, a condition associated with disruption of glycolytic flux and accumulation of sugar-phosphates. SgrS has been shown to stimulate degradation of the ptsG mRNA, encoding the major glucose transporter. This study demonstrates that SgrS regulates the genes encoding the mannose and secondary glucose transporter, manXYZ. Analysis of manXYZ mRNA stability and translation in the presence and absence of SgrS indicate that manXYZ is regulated by SgrS under stress conditions and when SgrS is ectopically expressed. In vitro footprinting and in vivo mutational analyses showed that SgrS base pairs with manXYZ within the manX coding sequence to prevent manX translation. Regulation of manX did not require the RNase E degradosome complex, suggesting that the primary mechanism of regulation is translational. An Escherichia coli ptsG mutant strain that is manXYZ(+) experiences stress when exposed to the glucose analogs α- methyl glucoside or 2-deoxyglucose. A ptsG manXYZ double mutant is resistant to the stress, indicating that PTS transporters encoded by both SgrS targets are involved in taking up substrates that cause stress. We further demonstrate that SgrS binds to two sites on the manXYZ mRNA to coordinately down-regulate translation of all the cistrons, a mechanism reminiscent of that used by the eukaryotic miRNA, lin-4 for regulation of the lin-14 mRNA. We tested the hypothesis that regulation of manY and manZ is dependent on SgrS:manX base pairing and subsequent manXYZ mRNA degradation. Contrary to the hypothesis, we show that SgrS repression of iii manY and manZ translation can be decoupled from SgrS-dependent manXYZ mRNA degradation. Furthermore, SgrS regulates manY translation by a mechanism that is independent of SgrS:manX mRNA interactions. Instead, translational regulation of manY depends on SgrS pairing with sequences in the manX-manY intergenic region, upstream of the manY ribosome binding site. Mutational analysis suggests that while the SgrS-manY interaction is sufficient to stimulate some degradation of the manXYZ mRNA, pairing with both sites is required for maximal degradation of the manXYZ mRNA. Additional SgrS candidate-mRNA targets are also investigated.","abstract_has_math":false,"creators":["Rice, Jennifer"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Microbiology","degree_department":null,"school":null,"contributors":["Vanderpool, Carin K.","Farrand, Stephen K.","Cronan, John E.","Miller, Charles G."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2012,"date_issued":"2012-02-01T00:55:23Z","date_published":"2012-02-01T00:55:23Z","updated_at":"2026-07-22T22:25:27Z","subjects":["small RNA (sRNA)","sugar transport-related sRNA (SgrS)","manXYZ","glucose-phosphate stress","Ribonucleic acid (RNA)"],"languages":["en"],"rights":["Copyright 2011 Jennifer Rice"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/29559","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Vanderpool, Carin K.","Farrand, Stephen K.","Cronan, John E.","Miller, Charles G."]},{"key":"dc:creator","label":"Author","values":["Rice, Jennifer"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2012-02-01T00:55:23Z","2014-02-01T11:00:34Z","2011-12"]},{"key":"dc:type","label":"Dc Type","values":["Dissertation / Thesis","text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Microbiology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["small RNA (sRNA)","sugar transport-related sRNA (SgrS)","manXYZ","glucose-phosphate stress","Ribonucleic acid (RNA)"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2011 Jennifer Rice"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/29559"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["A number of bacterial small RNAs (sRNAs) act as global regulators of stress responses by controlling expression of multiple genes. The sRNA SgrS is expressed in response to glucose-phosphate stress, a condition associated with disruption of glycolytic flux and accumulation of sugar-phosphates. SgrS has been shown to stimulate degradation of the ptsG mRNA, encoding the major glucose transporter. This study demonstrates that SgrS regulates the genes encoding the mannose and secondary glucose transporter, manXYZ. Analysis of manXYZ mRNA stability and translation in the presence and absence of SgrS indicate that manXYZ is regulated by SgrS under stress conditions and when SgrS is ectopically expressed. In vitro footprinting and in vivo mutational analyses showed that SgrS base pairs with manXYZ within the manX coding sequence to prevent manX translation. Regulation of manX did not require the RNase E degradosome complex, suggesting that the primary mechanism of regulation is translational. An Escherichia coli ptsG mutant strain that is manXYZ(+) experiences stress when exposed to the glucose analogs α- methyl glucoside or 2-deoxyglucose. A ptsG manXYZ double mutant is resistant to the stress, indicating that PTS transporters encoded by both SgrS targets are involved in taking up substrates that cause stress. We further demonstrate that SgrS binds to two sites on the manXYZ mRNA to coordinately down-regulate translation of all the cistrons, a mechanism reminiscent of that used by the eukaryotic miRNA, lin-4 for regulation of the lin-14 mRNA. We tested the hypothesis that regulation of manY and manZ is dependent on SgrS:manX base pairing and subsequent manXYZ mRNA degradation. Contrary to the hypothesis, we show that SgrS repression of iii manY and manZ translation can be decoupled from SgrS-dependent manXYZ mRNA degradation. Furthermore, SgrS regulates manY translation by a mechanism that is independent of SgrS:manX mRNA interactions. Instead, translational regulation of manY depends on SgrS pairing with sequences in the manX-manY intergenic region, upstream of the manY ribosome binding site. Mutational analysis suggests that while the SgrS-manY interaction is sufficient to stimulate some degradation of the manXYZ mRNA, pairing with both sites is required for maximal degradation of the manXYZ mRNA. Additional SgrS candidate-mRNA targets are also investigated.","Item withdrawn by Rebecca Bryant (rabryant@illinois.edu) on 2011-12-01T18:58:57Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 1 Rice_Jennifer.pdf: 6720791 bytes, checksum: 39886c7788e7ce789b52f2ae9a801f21 (MD5)","Made available in DSpace on 2012-02-01T00:55:23Z (GMT). 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The sRNA SgrS is expressed in response to glucose-phosphate stress, a condition associated with disruption of glycolytic flux and accumulation of sugar-phosphates. SgrS has been shown to stimulate degradation of the ptsG mRNA, encoding the major glucose transporter. This study demonstrates that SgrS regulates the genes encoding the mannose and secondary glucose transporter, manXYZ. Analysis of manXYZ mRNA stability and translation in the presence and absence of SgrS indicate that manXYZ is regulated by SgrS under stress conditions and when SgrS is ectopically expressed. In vitro footprinting and in vivo mutational analyses showed that SgrS base pairs with manXYZ within the manX coding sequence to prevent manX translation. Regulation of manX did not require the RNase E degradosome complex, suggesting that the primary mechanism of regulation is translational. An Escherichia coli ptsG mutant strain that is manXYZ(+) experiences stress when exposed to the glucose analogs α- methyl glucoside or 2-deoxyglucose. A ptsG manXYZ double mutant is resistant to the stress, indicating that PTS transporters encoded by both SgrS targets are involved in taking up substrates that cause stress. We further demonstrate that SgrS binds to two sites on the manXYZ mRNA to coordinately down-regulate translation of all the cistrons, a mechanism reminiscent of that used by the eukaryotic miRNA, lin-4 for regulation of the lin-14 mRNA. We tested the hypothesis that regulation of manY and manZ is dependent on SgrS:manX base pairing and subsequent manXYZ mRNA degradation. Contrary to the hypothesis, we show that SgrS repression of iii manY and manZ translation can be decoupled from SgrS-dependent manXYZ mRNA degradation. Furthermore, SgrS regulates manY translation by a mechanism that is independent of SgrS:manX mRNA interactions. Instead, translational regulation of manY depends on SgrS pairing with sequences in the manX-manY intergenic region, upstream of the manY ribosome binding site. Mutational analysis suggests that while the SgrS-manY interaction is sufficient to stimulate some degradation of the manXYZ mRNA, pairing with both sites is required for maximal degradation of the manXYZ mRNA. Additional SgrS candidate-mRNA targets are also investigated.","Item withdrawn by Rebecca Bryant (rabryant@illinois.edu) on 2011-12-01T18:58:57Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 1 Rice_Jennifer.pdf: 6720791 bytes, checksum: 39886c7788e7ce789b52f2ae9a801f21 (MD5)","Made available in DSpace on 2012-02-01T00:55:23Z (GMT). No. of bitstreams: 2 Rice_Jennifer.pdf: 6720791 bytes, checksum: 39886c7788e7ce789b52f2ae9a801f21 (MD5) license.txt: 4062 bytes, checksum: 561ccc9f8a004ab8f4a7361d6d29555a (MD5)","Item marked as restricted to the 'Administrator' Group (id=1) by William Ingram (wingram2@illinois.edu) on 2012-02-01T00:57:09Z Item is restricted until 2014-02-01T00:56:58Z","Item reinstated by Sarah Shreeves (sshreeve@illinois.edu) on 2014-02-01T11:00:34Z Item was in collections: Graduate Theses and Dissertations at Illinois (ID: 204) Dissertations - Microbiology (ID: 748) No. of bitstreams: 2 Rice_Jennifer.pdf: 6720791 bytes, checksum: 39886c7788e7ce789b52f2ae9a801f21 (MD5) license.txt: 4062 bytes, checksum: 561ccc9f8a004ab8f4a7361d6d29555a (MD5)","Item released from any restrictions by Sarah Shreeves (sshreeve@illinois.edu) on 2014-02-01T11:00:34Z"],"dc:identifier":["http://hdl.handle.net/2142/29559"],"dc:language":["en"],"dc:rights":["Copyright 2011 Jennifer Rice"],"dc:subject":["small RNA (sRNA)","sugar transport-related sRNA (SgrS)","manXYZ","glucose-phosphate stress","Ribonucleic acid (RNA)"],"dc:title":["Regulation of the Mannose PTS Operon by the small RNA SgrS"],"dc:type":["Dissertation / Thesis","text"],"thesis:degree_discipline":["Microbiology"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:25:27Z"}