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Helicobacter pylori Activates the Histidine Decarboxylase Promoter through a Mitogen-activated Protein Kinase Pathway Independent of Pathogenicity Island-encoded Virulence Factors
Helicobacter pylori infection of the gastric mucosa is accompanied by an activated histamine metabolism. Histamine plays a central role in the regulation of gastric acid secretion and is involved in the pathogenesis of gastroduodenal ulcerations. Histidine decarboxylase (HDC) is the rate-limiting en...
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Published in: | The Journal of biological chemistry 2000-02, Vol.275 (5), p.3629-3636 |
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description | Helicobacter pylori infection of the gastric mucosa is accompanied by an activated histamine metabolism. Histamine plays a central role in the regulation of gastric acid secretion and is involved in the pathogenesis of gastroduodenal ulcerations. Histidine decarboxylase (HDC) is the rate-limiting enzyme for histamine production, and its activity is regulated through transcriptional mechanisms. The present study investigated the effect of H. pylori infection on the transcriptional activity of the human HDC (hHDC) promoter in a gastric epithelial cell line (AGS) and analyzed the underlying molecular mechanisms. Our studies demonstrate that H. pylori infection potently transactivated the hHDC promoter. The H. pylori-responsive element of the hHDC gene was mapped to the sequence +1 to +27 base pairs, which shows no homology to known cis-acting elements and also functions as a gastrin-responsive element. H. pylori regulates the activity of this element via a Raf-1/MEK/ERK pathway, which was activated in a Ras-independent manner. Furthermore, we found that H. pylori-induced transactivation of the hHDC promoter was independent of the cag pathogenicity island and the vacuolating cytotoxin A gene and therefore may be exerted through (a) new virulence factor(s). A better understanding of H. pylori-directed hHDC transcription can provide novel insights into the molecular mechanisms of H. pylori-dependent gene regulation in gastric epithelial cells and may lead to new therapeutic approaches. |
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Histamine plays a central role in the regulation of gastric acid secretion and is involved in the pathogenesis of gastroduodenal ulcerations. Histidine decarboxylase (HDC) is the rate-limiting enzyme for histamine production, and its activity is regulated through transcriptional mechanisms. The present study investigated the effect of H. pylori infection on the transcriptional activity of the human HDC (hHDC) promoter in a gastric epithelial cell line (AGS) and analyzed the underlying molecular mechanisms. Our studies demonstrate that H. pylori infection potently transactivated the hHDC promoter. The H. pylori-responsive element of the hHDC gene was mapped to the sequence +1 to +27 base pairs, which shows no homology to known cis-acting elements and also functions as a gastrin-responsive element. H. pylori regulates the activity of this element via a Raf-1/MEK/ERK pathway, which was activated in a Ras-independent manner. Furthermore, we found that H. pylori-induced transactivation of the hHDC promoter was independent of the cag pathogenicity island and the vacuolating cytotoxin A gene and therefore may be exerted through (a) new virulence factor(s). A better understanding of H. pylori-directed hHDC transcription can provide novel insights into the molecular mechanisms of H. pylori-dependent gene regulation in gastric epithelial cells and may lead to new therapeutic approaches.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.275.5.3629</identifier><identifier>PMID: 10652359</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>cag gene ; cytotoxin A ; Helicobacter pylori ; Helicobacter pylori - metabolism ; Helicobacter pylori - pathogenicity ; hHDC gene ; histamine ; Histidine Decarboxylase - genetics ; Histidine Decarboxylase - metabolism ; Humans ; MAP Kinase Signaling System ; Promoter Regions, Genetic ; Ras protein ; Signal Transduction ; Virulence</subject><ispartof>The Journal of biological chemistry, 2000-02, Vol.275 (5), p.3629-3636</ispartof><rights>2000 © 2000 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-8808997e9901777aaf1a459dc7a9c3732f1ebf9f2cc0feddeb0c130b1c0940e13</citedby><cites>FETCH-LOGICAL-c533t-8808997e9901777aaf1a459dc7a9c3732f1ebf9f2cc0feddeb0c130b1c0940e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021925818309487$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3535,27903,27904,45759</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10652359$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wessler, Silja</creatorcontrib><creatorcontrib>Höcker, Michael</creatorcontrib><creatorcontrib>Fischer, Wolfgang</creatorcontrib><creatorcontrib>Wang, Timothy C.</creatorcontrib><creatorcontrib>Rosewicz, Stefan</creatorcontrib><creatorcontrib>Haas, Rainer</creatorcontrib><creatorcontrib>Wiedenmann, Bertram</creatorcontrib><creatorcontrib>Meyer, Thomas F.</creatorcontrib><creatorcontrib>Naumann, Michael</creatorcontrib><title>Helicobacter pylori Activates the Histidine Decarboxylase Promoter through a Mitogen-activated Protein Kinase Pathway Independent of Pathogenicity Island-encoded Virulence Factors</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Helicobacter pylori infection of the gastric mucosa is accompanied by an activated histamine metabolism. Histamine plays a central role in the regulation of gastric acid secretion and is involved in the pathogenesis of gastroduodenal ulcerations. Histidine decarboxylase (HDC) is the rate-limiting enzyme for histamine production, and its activity is regulated through transcriptional mechanisms. The present study investigated the effect of H. pylori infection on the transcriptional activity of the human HDC (hHDC) promoter in a gastric epithelial cell line (AGS) and analyzed the underlying molecular mechanisms. Our studies demonstrate that H. pylori infection potently transactivated the hHDC promoter. The H. pylori-responsive element of the hHDC gene was mapped to the sequence +1 to +27 base pairs, which shows no homology to known cis-acting elements and also functions as a gastrin-responsive element. H. pylori regulates the activity of this element via a Raf-1/MEK/ERK pathway, which was activated in a Ras-independent manner. Furthermore, we found that H. pylori-induced transactivation of the hHDC promoter was independent of the cag pathogenicity island and the vacuolating cytotoxin A gene and therefore may be exerted through (a) new virulence factor(s). A better understanding of H. pylori-directed hHDC transcription can provide novel insights into the molecular mechanisms of H. pylori-dependent gene regulation in gastric epithelial cells and may lead to new therapeutic approaches.</description><subject>cag gene</subject><subject>cytotoxin A</subject><subject>Helicobacter pylori</subject><subject>Helicobacter pylori - metabolism</subject><subject>Helicobacter pylori - pathogenicity</subject><subject>hHDC gene</subject><subject>histamine</subject><subject>Histidine Decarboxylase - genetics</subject><subject>Histidine Decarboxylase - metabolism</subject><subject>Humans</subject><subject>MAP Kinase Signaling System</subject><subject>Promoter Regions, Genetic</subject><subject>Ras protein</subject><subject>Signal Transduction</subject><subject>Virulence</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhS0EokvhyhFZHLgl2HFcx8eqpWxFERwAcbMce7JxlcSL7bTs7-IP4jR7gAPCh7Hs-d7TaB5CLykpKRH129vWlJXgJS_ZWSUfoQ0lDSsYp98fow0hFS1kxZsT9CzGW5JPLelTdELJGa8Ylxv0awuDM77VJkHA-8Pgg8PnJrk7nSDi1APeupicdRPgSzA6tP7nYdAR8OfgR7-oUh_8vOuxxh9d8juYCn00sAuUwE34g5seNDr19_qArycLe8hlSth3D9-L0BmXcjMOerIFTMbbbPHNhXnID8BX2deH-Bw96fQQ4cXxPkVfr959udgWN5_eX1-c3xSGM5aKpiGNlAKkJFQIoXVHdc2lNUJLwwSrOgptJ7vKGNKBtdASQxlpqSGyJkDZKXqz-u6D_zFDTGp00cCQpwM_RyVII0RN_g9SUfOKNiyD5Qqa4GMM0Kl9cKMOB0WJWvJUOU-V81RcLXlmwauj89yOYP_A1wAz8HoFerfr710A1Tpvehj_dmlWCPK27hwEFY1bNmqzwCRlvfvXAL8BVuy_MQ</recordid><startdate>20000204</startdate><enddate>20000204</enddate><creator>Wessler, Silja</creator><creator>Höcker, Michael</creator><creator>Fischer, Wolfgang</creator><creator>Wang, Timothy C.</creator><creator>Rosewicz, Stefan</creator><creator>Haas, Rainer</creator><creator>Wiedenmann, Bertram</creator><creator>Meyer, Thomas F.</creator><creator>Naumann, Michael</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><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>7QL</scope><scope>7TM</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20000204</creationdate><title>Helicobacter pylori Activates the Histidine Decarboxylase Promoter through a Mitogen-activated Protein Kinase Pathway Independent of Pathogenicity Island-encoded Virulence Factors</title><author>Wessler, Silja ; 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Histamine plays a central role in the regulation of gastric acid secretion and is involved in the pathogenesis of gastroduodenal ulcerations. Histidine decarboxylase (HDC) is the rate-limiting enzyme for histamine production, and its activity is regulated through transcriptional mechanisms. The present study investigated the effect of H. pylori infection on the transcriptional activity of the human HDC (hHDC) promoter in a gastric epithelial cell line (AGS) and analyzed the underlying molecular mechanisms. Our studies demonstrate that H. pylori infection potently transactivated the hHDC promoter. The H. pylori-responsive element of the hHDC gene was mapped to the sequence +1 to +27 base pairs, which shows no homology to known cis-acting elements and also functions as a gastrin-responsive element. H. pylori regulates the activity of this element via a Raf-1/MEK/ERK pathway, which was activated in a Ras-independent manner. Furthermore, we found that H. pylori-induced transactivation of the hHDC promoter was independent of the cag pathogenicity island and the vacuolating cytotoxin A gene and therefore may be exerted through (a) new virulence factor(s). A better understanding of H. pylori-directed hHDC transcription can provide novel insights into the molecular mechanisms of H. pylori-dependent gene regulation in gastric epithelial cells and may lead to new therapeutic approaches.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10652359</pmid><doi>10.1074/jbc.275.5.3629</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | cag gene cytotoxin A Helicobacter pylori Helicobacter pylori - metabolism Helicobacter pylori - pathogenicity hHDC gene histamine Histidine Decarboxylase - genetics Histidine Decarboxylase - metabolism Humans MAP Kinase Signaling System Promoter Regions, Genetic Ras protein Signal Transduction Virulence |
title | Helicobacter pylori Activates the Histidine Decarboxylase Promoter through a Mitogen-activated Protein Kinase Pathway Independent of Pathogenicity Island-encoded Virulence Factors |
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