Expression of 3-hydroxy-3-methylglutaryl-CoA reductase, p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [Arnebia euchroma (Royle) Johnston]
Geranyl pyrophosphate (GPP) and p-hydroxybenzoate (PHB) are the basic precursors involved in shikonins biosynthesis. GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however,...
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description | Geranyl pyrophosphate (GPP) and p-hydroxybenzoate (PHB) are the basic precursors involved in shikonins biosynthesis. GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however, is synthesized by only phenylpropanoid (PP) pathway. GPP and PHB are central moieties to yield shikonins through the synthesis of m-geranyl-p-hydroxybenzoate (GHB). Enzyme p-hydroxybenzoate-m-geranyltransferase (PGT) catalyses the coupling of GPP and PHB to yield GHB. The present research was carried out in shikonins yielding plant arnebia [Arnebia euchroma (Royle) Johnston], wherein no molecular work has been reported so far. The objective of the work was to identify the preferred GPP synthesizing pathway for shikonins biosynthesis, and to determine the regulatory genes involved in the biosynthesis of GPP, PHB and GHB.
A cell suspension culture-based, low and high shikonins production systems were developed to facilitate pathway identification and finding the regulatory gene. Studies with mevinolin and fosmidomycin, inhibitors of MVA and MEP pathway, respectively suggested MVA as a preferred route of GPP supply for shikonins biosynthesis in arnebia. Accordingly, genes of MVA pathway (eight genes), PP pathway (three genes), and GHB biosynthesis were cloned. Expression studies showed down-regulation of all the genes in response to mevinolin treatment, whereas gene expression was not influenced by fosmidomycin. Expression of all the twelve genes vis-à-vis shikonins content in low and high shikonins production system, over a period of twelve days at frequent intervals, identified critical genes of shikonins biosynthesis in arnebia.
A positive correlation between shikonins content and expression of 3-hydroxy-3-methylglutaryl-CoA reductase (AeHMGR) and AePGT suggested critical role played by these genes in shikonins biosynthesis. Higher expression of genes of PP pathway was a general feature for higher shikonins biosynthesis. |
doi_str_mv | 10.1186/1471-2199-11-88 |
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A cell suspension culture-based, low and high shikonins production systems were developed to facilitate pathway identification and finding the regulatory gene. Studies with mevinolin and fosmidomycin, inhibitors of MVA and MEP pathway, respectively suggested MVA as a preferred route of GPP supply for shikonins biosynthesis in arnebia. Accordingly, genes of MVA pathway (eight genes), PP pathway (three genes), and GHB biosynthesis were cloned. Expression studies showed down-regulation of all the genes in response to mevinolin treatment, whereas gene expression was not influenced by fosmidomycin. Expression of all the twelve genes vis-à-vis shikonins content in low and high shikonins production system, over a period of twelve days at frequent intervals, identified critical genes of shikonins biosynthesis in arnebia.
A positive correlation between shikonins content and expression of 3-hydroxy-3-methylglutaryl-CoA reductase (AeHMGR) and AePGT suggested critical role played by these genes in shikonins biosynthesis. Higher expression of genes of PP pathway was a general feature for higher shikonins biosynthesis.</description><identifier>ISSN: 1471-2199</identifier><identifier>EISSN: 1471-2199</identifier><identifier>DOI: 10.1186/1471-2199-11-88</identifier><identifier>PMID: 21092138</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Biosynthesis ; Boraginaceae - enzymology ; Boraginaceae - genetics ; Boraginaceae - metabolism ; Cloning ; Data collection ; Gene Expression Regulation, Plant ; Genes ; Genes, Plant ; Genetic aspects ; Geranyltranstransferase - genetics ; Geranyltranstransferase - metabolism ; Hydroxymethylglutaryl CoA Reductases - genetics ; Hydroxymethylglutaryl CoA Reductases - metabolism ; Industrial research ; Naphthoquinones - metabolism ; Parabens - metabolism ; Physiological aspects ; Phytochemicals ; Polyisoprenyl Phosphates - metabolism ; Tissue engineering</subject><ispartof>BMC molecular biology, 2010-11, Vol.11 (1), p.88-88, Article 88</ispartof><rights>COPYRIGHT 2010 BioMed Central Ltd.</rights><rights>2010 Singh et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2010 Singh et al; licensee BioMed Central Ltd. 2010 Singh et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b538t-89e31718176cbe34686cf84618028da7bbe22155c3181574c063cbb999f2fa8e3</citedby><cites>FETCH-LOGICAL-b538t-89e31718176cbe34686cf84618028da7bbe22155c3181574c063cbb999f2fa8e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002352/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002352/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,24780,27901,27902,53766,53768,75707,75708</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21092138$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh, Ravi S</creatorcontrib><creatorcontrib>Gara, Rishi K</creatorcontrib><creatorcontrib>Bhardwaj, Pardeep K</creatorcontrib><creatorcontrib>Kaachra, Anish</creatorcontrib><creatorcontrib>Malik, Sonia</creatorcontrib><creatorcontrib>Kumar, Ravi</creatorcontrib><creatorcontrib>Sharma, Madhu</creatorcontrib><creatorcontrib>Ahuja, Paramvir S</creatorcontrib><creatorcontrib>Kumar, Sanjay</creatorcontrib><title>Expression of 3-hydroxy-3-methylglutaryl-CoA reductase, p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [Arnebia euchroma (Royle) Johnston]</title><title>BMC molecular biology</title><addtitle>BMC Mol Biol</addtitle><description>Geranyl pyrophosphate (GPP) and p-hydroxybenzoate (PHB) are the basic precursors involved in shikonins biosynthesis. GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however, is synthesized by only phenylpropanoid (PP) pathway. GPP and PHB are central moieties to yield shikonins through the synthesis of m-geranyl-p-hydroxybenzoate (GHB). Enzyme p-hydroxybenzoate-m-geranyltransferase (PGT) catalyses the coupling of GPP and PHB to yield GHB. The present research was carried out in shikonins yielding plant arnebia [Arnebia euchroma (Royle) Johnston], wherein no molecular work has been reported so far. The objective of the work was to identify the preferred GPP synthesizing pathway for shikonins biosynthesis, and to determine the regulatory genes involved in the biosynthesis of GPP, PHB and GHB.
A cell suspension culture-based, low and high shikonins production systems were developed to facilitate pathway identification and finding the regulatory gene. Studies with mevinolin and fosmidomycin, inhibitors of MVA and MEP pathway, respectively suggested MVA as a preferred route of GPP supply for shikonins biosynthesis in arnebia. Accordingly, genes of MVA pathway (eight genes), PP pathway (three genes), and GHB biosynthesis were cloned. Expression studies showed down-regulation of all the genes in response to mevinolin treatment, whereas gene expression was not influenced by fosmidomycin. Expression of all the twelve genes vis-à-vis shikonins content in low and high shikonins production system, over a period of twelve days at frequent intervals, identified critical genes of shikonins biosynthesis in arnebia.
A positive correlation between shikonins content and expression of 3-hydroxy-3-methylglutaryl-CoA reductase (AeHMGR) and AePGT suggested critical role played by these genes in shikonins biosynthesis. Higher expression of genes of PP pathway was a general feature for higher shikonins biosynthesis.</description><subject>Biosynthesis</subject><subject>Boraginaceae - enzymology</subject><subject>Boraginaceae - genetics</subject><subject>Boraginaceae - metabolism</subject><subject>Cloning</subject><subject>Data collection</subject><subject>Gene Expression Regulation, Plant</subject><subject>Genes</subject><subject>Genes, Plant</subject><subject>Genetic aspects</subject><subject>Geranyltranstransferase - genetics</subject><subject>Geranyltranstransferase - metabolism</subject><subject>Hydroxymethylglutaryl CoA Reductases - genetics</subject><subject>Hydroxymethylglutaryl CoA Reductases - metabolism</subject><subject>Industrial research</subject><subject>Naphthoquinones - metabolism</subject><subject>Parabens - metabolism</subject><subject>Physiological aspects</subject><subject>Phytochemicals</subject><subject>Polyisoprenyl Phosphates - metabolism</subject><subject>Tissue engineering</subject><issn>1471-2199</issn><issn>1471-2199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkluL1TAUhYsozjj67JsEfVDBOrn0kr4Ix8N4Y0AQfRIJabp7mrFNapLOnPqH_RumnDPDjCi-JJusj8XaOztJHhL8khBeHJOsJCklVZUSknJ-Kzm8erl9rT5I7nl_hjEpOeN3kwNKcEUJ44fJr5Pt6MB7bQ2yLWJpNzfObueUpQOEbu43_RSkm_t0bVfIQTOpID28QOMlWYP5aWWAdEg34KSZ-xBP38baA5KmQRsw4Bf3sYMoj86O0ljdoFGG7kLOCLadrnXwaLReB30OSFnnoJdhiXWhQ4d8p79bo42PkglgAtIGSWeg1hJ9Xe0LmFTn7CDRs0927uE5-mA744M13-4nd1rZe3iwv4-SL29OPq_fpacf375fr07TOmc8pLwCRkrCSVmoGlhW8EK1PCsIx5Q3sqxroJTkuWKRyctM4YKpuq6qqqWt5MCOklc733GqB2hUTOpkL0anhzhFYaUWNxWjO7Gx54JhTFlOo8HrnUGt7T8MbirKDmL5aLF8tCBEcB5Nnu5TOPtjAh_EoL2CvpcG7ORFlWcF5hUv_0vyuGUZjj1H8vEf5JmdnInDFBWmOCtZVkXoyQ7ayB6ENq2NGdViKVY0y8qSULZQxztKOeu9g_aqPYLFstd_aejR9bFe8ZeLzH4DofT52A</recordid><startdate>20101121</startdate><enddate>20101121</enddate><creator>Singh, Ravi S</creator><creator>Gara, Rishi K</creator><creator>Bhardwaj, Pardeep K</creator><creator>Kaachra, Anish</creator><creator>Malik, Sonia</creator><creator>Kumar, Ravi</creator><creator>Sharma, Madhu</creator><creator>Ahuja, Paramvir S</creator><creator>Kumar, Sanjay</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>3V.</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</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>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20101121</creationdate><title>Expression of 3-hydroxy-3-methylglutaryl-CoA reductase, p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [Arnebia euchroma (Royle) Johnston]</title><author>Singh, Ravi S ; Gara, Rishi K ; Bhardwaj, Pardeep K ; Kaachra, Anish ; Malik, Sonia ; Kumar, Ravi ; Sharma, Madhu ; Ahuja, Paramvir S ; Kumar, Sanjay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b538t-89e31718176cbe34686cf84618028da7bbe22155c3181574c063cbb999f2fa8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biosynthesis</topic><topic>Boraginaceae - enzymology</topic><topic>Boraginaceae - genetics</topic><topic>Boraginaceae - metabolism</topic><topic>Cloning</topic><topic>Data collection</topic><topic>Gene Expression Regulation, Plant</topic><topic>Genes</topic><topic>Genes, Plant</topic><topic>Genetic aspects</topic><topic>Geranyltranstransferase - genetics</topic><topic>Geranyltranstransferase - metabolism</topic><topic>Hydroxymethylglutaryl CoA Reductases - genetics</topic><topic>Hydroxymethylglutaryl CoA Reductases - metabolism</topic><topic>Industrial research</topic><topic>Naphthoquinones - metabolism</topic><topic>Parabens - metabolism</topic><topic>Physiological aspects</topic><topic>Phytochemicals</topic><topic>Polyisoprenyl Phosphates - metabolism</topic><topic>Tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Ravi S</creatorcontrib><creatorcontrib>Gara, Rishi K</creatorcontrib><creatorcontrib>Bhardwaj, Pardeep K</creatorcontrib><creatorcontrib>Kaachra, Anish</creatorcontrib><creatorcontrib>Malik, Sonia</creatorcontrib><creatorcontrib>Kumar, Ravi</creatorcontrib><creatorcontrib>Sharma, Madhu</creatorcontrib><creatorcontrib>Ahuja, Paramvir S</creatorcontrib><creatorcontrib>Kumar, Sanjay</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - 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GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however, is synthesized by only phenylpropanoid (PP) pathway. GPP and PHB are central moieties to yield shikonins through the synthesis of m-geranyl-p-hydroxybenzoate (GHB). Enzyme p-hydroxybenzoate-m-geranyltransferase (PGT) catalyses the coupling of GPP and PHB to yield GHB. The present research was carried out in shikonins yielding plant arnebia [Arnebia euchroma (Royle) Johnston], wherein no molecular work has been reported so far. The objective of the work was to identify the preferred GPP synthesizing pathway for shikonins biosynthesis, and to determine the regulatory genes involved in the biosynthesis of GPP, PHB and GHB.
A cell suspension culture-based, low and high shikonins production systems were developed to facilitate pathway identification and finding the regulatory gene. Studies with mevinolin and fosmidomycin, inhibitors of MVA and MEP pathway, respectively suggested MVA as a preferred route of GPP supply for shikonins biosynthesis in arnebia. Accordingly, genes of MVA pathway (eight genes), PP pathway (three genes), and GHB biosynthesis were cloned. Expression studies showed down-regulation of all the genes in response to mevinolin treatment, whereas gene expression was not influenced by fosmidomycin. Expression of all the twelve genes vis-à-vis shikonins content in low and high shikonins production system, over a period of twelve days at frequent intervals, identified critical genes of shikonins biosynthesis in arnebia.
A positive correlation between shikonins content and expression of 3-hydroxy-3-methylglutaryl-CoA reductase (AeHMGR) and AePGT suggested critical role played by these genes in shikonins biosynthesis. Higher expression of genes of PP pathway was a general feature for higher shikonins biosynthesis.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>21092138</pmid><doi>10.1186/1471-2199-11-88</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biosynthesis Boraginaceae - enzymology Boraginaceae - genetics Boraginaceae - metabolism Cloning Data collection Gene Expression Regulation, Plant Genes Genes, Plant Genetic aspects Geranyltranstransferase - genetics Geranyltranstransferase - metabolism Hydroxymethylglutaryl CoA Reductases - genetics Hydroxymethylglutaryl CoA Reductases - metabolism Industrial research Naphthoquinones - metabolism Parabens - metabolism Physiological aspects Phytochemicals Polyisoprenyl Phosphates - metabolism Tissue engineering |
title | Expression of 3-hydroxy-3-methylglutaryl-CoA reductase, p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [Arnebia euchroma (Royle) Johnston] |
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