Characterization of the dry bean polygaiacturonase-inhibiting protein (PGIP) gene family during Sclerotinia sclerotiorum (Sderotiniaceae) infection
Polygaiacturonase-inhibiting proteins are leucine-rich repeat proteins that inhibit fungal endopolygalacturonases. The interaction of polygaiacturonase-inhibiting protein with endopolygalacturonases limits the destructive potential of endopolygalacturonases and may trigger plant defense responses in...
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Veröffentlicht in: | Genetics and molecular research 2010-01, Vol.9 (2), p.994-1004 |
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description | Polygaiacturonase-inhibiting proteins are leucine-rich repeat proteins that inhibit fungal endopolygalacturonases. The interaction of polygaiacturonase-inhibiting protein with endopolygalacturonases limits the destructive potential of endopolygalacturonases and may trigger plant defense responses induced by oligogalacturonides. We examined the expression of fungal pg and plant Pvpgip genes in bean (Phaseolus vulgaris) stems infected with Sclerotinia sclerotiorum to determine whether any of them are associated with the infection process. Transcriptional analysis was carried out by means of semi-quantitative reverse transcription PCR or real-time PCR. The sspg1 gene was highly expressed during infection; sspg3 was regulated during the later phases of infection; sspg5 was more uniformly expressed during infection, whereas sspg6 was only weakly expressed. During the course of infection, Pvpgip1 transcripts were not detected at early stages, but they appeared 72 h post-inoculation. High levels of Pvpgip2 expression were observed during the initial phase of infection; the transcript peaked by 48 h post-inoculation and declined by 72 h post-inoculation. Pvpgip3 expression increased strongly at 96 h post-inoculation. Pvpgip4 was constantly present from 24 h post-inoculation until the end of the experiment. However, we detected higher levels of the Pvpgip4 transcript in the necrotic lesion area than in plants that had been mechanically wounded. Remarkably, only Pvpgip4 appeared to be moderately induced by mechanical wounding. These results provide evidence that endopolygalacturonases contribute to the infection process during host colonization by promoting the release of plant cell oligogalacturonides, which are powerful signaling molecules and may also activate plant defenses, such as polygaiacturonase-inhibiting proteins. |
doi_str_mv | 10.4238/vol9-2gmr776 |
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The interaction of polygaiacturonase-inhibiting protein with endopolygalacturonases limits the destructive potential of endopolygalacturonases and may trigger plant defense responses induced by oligogalacturonides. We examined the expression of fungal pg and plant Pvpgip genes in bean (Phaseolus vulgaris) stems infected with Sclerotinia sclerotiorum to determine whether any of them are associated with the infection process. Transcriptional analysis was carried out by means of semi-quantitative reverse transcription PCR or real-time PCR. The sspg1 gene was highly expressed during infection; sspg3 was regulated during the later phases of infection; sspg5 was more uniformly expressed during infection, whereas sspg6 was only weakly expressed. During the course of infection, Pvpgip1 transcripts were not detected at early stages, but they appeared 72 h post-inoculation. High levels of Pvpgip2 expression were observed during the initial phase of infection; the transcript peaked by 48 h post-inoculation and declined by 72 h post-inoculation. Pvpgip3 expression increased strongly at 96 h post-inoculation. Pvpgip4 was constantly present from 24 h post-inoculation until the end of the experiment. However, we detected higher levels of the Pvpgip4 transcript in the necrotic lesion area than in plants that had been mechanically wounded. Remarkably, only Pvpgip4 appeared to be moderately induced by mechanical wounding. These results provide evidence that endopolygalacturonases contribute to the infection process during host colonization by promoting the release of plant cell oligogalacturonides, which are powerful signaling molecules and may also activate plant defenses, such as polygaiacturonase-inhibiting proteins.</description><identifier>ISSN: 1676-5680</identifier><identifier>EISSN: 1676-5680</identifier><identifier>DOI: 10.4238/vol9-2gmr776</identifier><language>eng</language><subject>Beans ; Colonization ; Endopolygalacturonase ; Host plants ; Infection ; oligogalacturonides ; pgip gene ; Phaseolus vulgaris ; Plant cells ; Polymerase chain reaction ; Reverse transcription ; Sclerotinia sclerotiorum ; Stems ; Transcription ; Wounding</subject><ispartof>Genetics and molecular research, 2010-01, Vol.9 (2), p.994-1004</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Oliveira, M B</creatorcontrib><creatorcontrib>Nascimento, L B</creatorcontrib><creatorcontrib>Junior, M L</creatorcontrib><creatorcontrib>Petrofeza, S</creatorcontrib><title>Characterization of the dry bean polygaiacturonase-inhibiting protein (PGIP) gene family during Sclerotinia sclerotiorum (Sderotiniaceae) infection</title><title>Genetics and molecular research</title><description>Polygaiacturonase-inhibiting proteins are leucine-rich repeat proteins that inhibit fungal endopolygalacturonases. The interaction of polygaiacturonase-inhibiting protein with endopolygalacturonases limits the destructive potential of endopolygalacturonases and may trigger plant defense responses induced by oligogalacturonides. We examined the expression of fungal pg and plant Pvpgip genes in bean (Phaseolus vulgaris) stems infected with Sclerotinia sclerotiorum to determine whether any of them are associated with the infection process. Transcriptional analysis was carried out by means of semi-quantitative reverse transcription PCR or real-time PCR. The sspg1 gene was highly expressed during infection; sspg3 was regulated during the later phases of infection; sspg5 was more uniformly expressed during infection, whereas sspg6 was only weakly expressed. During the course of infection, Pvpgip1 transcripts were not detected at early stages, but they appeared 72 h post-inoculation. High levels of Pvpgip2 expression were observed during the initial phase of infection; the transcript peaked by 48 h post-inoculation and declined by 72 h post-inoculation. Pvpgip3 expression increased strongly at 96 h post-inoculation. Pvpgip4 was constantly present from 24 h post-inoculation until the end of the experiment. However, we detected higher levels of the Pvpgip4 transcript in the necrotic lesion area than in plants that had been mechanically wounded. Remarkably, only Pvpgip4 appeared to be moderately induced by mechanical wounding. These results provide evidence that endopolygalacturonases contribute to the infection process during host colonization by promoting the release of plant cell oligogalacturonides, which are powerful signaling molecules and may also activate plant defenses, such as polygaiacturonase-inhibiting proteins.</description><subject>Beans</subject><subject>Colonization</subject><subject>Endopolygalacturonase</subject><subject>Host plants</subject><subject>Infection</subject><subject>oligogalacturonides</subject><subject>pgip gene</subject><subject>Phaseolus vulgaris</subject><subject>Plant cells</subject><subject>Polymerase chain reaction</subject><subject>Reverse transcription</subject><subject>Sclerotinia sclerotiorum</subject><subject>Stems</subject><subject>Transcription</subject><subject>Wounding</subject><issn>1676-5680</issn><issn>1676-5680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFj89Kw0AYxBdRsFZvPsDebA_R7CbZP0cpWgsFC-29fEm-TVfS3bqbCPU1fGFbrODN0wzMj2GGkFuW3uc8Uw8fvtUJb7ZBSnFGBkxIkRRCped__CW5ivEtTXmRq3RAviYbCFB1GOwndNY76g3tNkjrsKclgqM73-4bsAemD95BxMS6jS1tZ11Dd8F3aB0dLaazxZg26JAa2Np2T-s-HIll1eIBss4CjSfvQ7-lo2X9G1QIOKbWGayOE67JhYE24s1Jh2T1_LSavCTz1-ls8jhPdiJXiSnQyJIzCbkuClVjLYGZioFIMy6rEmWpOEgmjOGlkULwUmulMqg5x0KKbEjufmoPJ957jN16a2OFbQsOfR_XmjEmhGbqX1IJXehUZTz7BnJdeow</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Oliveira, M B</creator><creator>Nascimento, L B</creator><creator>Junior, M L</creator><creator>Petrofeza, S</creator><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20100101</creationdate><title>Characterization of the dry bean polygaiacturonase-inhibiting protein (PGIP) gene family during Sclerotinia sclerotiorum (Sderotiniaceae) infection</title><author>Oliveira, M B ; Nascimento, L B ; Junior, M L ; Petrofeza, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p648-f5ef7b217a49558ded7a1fc1a60327cbe7b82a716ff2bf7662b99883ad22e5763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Beans</topic><topic>Colonization</topic><topic>Endopolygalacturonase</topic><topic>Host plants</topic><topic>Infection</topic><topic>oligogalacturonides</topic><topic>pgip gene</topic><topic>Phaseolus vulgaris</topic><topic>Plant cells</topic><topic>Polymerase chain reaction</topic><topic>Reverse transcription</topic><topic>Sclerotinia sclerotiorum</topic><topic>Stems</topic><topic>Transcription</topic><topic>Wounding</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oliveira, M B</creatorcontrib><creatorcontrib>Nascimento, L B</creatorcontrib><creatorcontrib>Junior, M L</creatorcontrib><creatorcontrib>Petrofeza, S</creatorcontrib><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genetics and molecular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oliveira, M B</au><au>Nascimento, L B</au><au>Junior, M L</au><au>Petrofeza, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of the dry bean polygaiacturonase-inhibiting protein (PGIP) gene family during Sclerotinia sclerotiorum (Sderotiniaceae) infection</atitle><jtitle>Genetics and molecular research</jtitle><date>2010-01-01</date><risdate>2010</risdate><volume>9</volume><issue>2</issue><spage>994</spage><epage>1004</epage><pages>994-1004</pages><issn>1676-5680</issn><eissn>1676-5680</eissn><abstract>Polygaiacturonase-inhibiting proteins are leucine-rich repeat proteins that inhibit fungal endopolygalacturonases. The interaction of polygaiacturonase-inhibiting protein with endopolygalacturonases limits the destructive potential of endopolygalacturonases and may trigger plant defense responses induced by oligogalacturonides. We examined the expression of fungal pg and plant Pvpgip genes in bean (Phaseolus vulgaris) stems infected with Sclerotinia sclerotiorum to determine whether any of them are associated with the infection process. Transcriptional analysis was carried out by means of semi-quantitative reverse transcription PCR or real-time PCR. The sspg1 gene was highly expressed during infection; sspg3 was regulated during the later phases of infection; sspg5 was more uniformly expressed during infection, whereas sspg6 was only weakly expressed. During the course of infection, Pvpgip1 transcripts were not detected at early stages, but they appeared 72 h post-inoculation. High levels of Pvpgip2 expression were observed during the initial phase of infection; the transcript peaked by 48 h post-inoculation and declined by 72 h post-inoculation. Pvpgip3 expression increased strongly at 96 h post-inoculation. Pvpgip4 was constantly present from 24 h post-inoculation until the end of the experiment. However, we detected higher levels of the Pvpgip4 transcript in the necrotic lesion area than in plants that had been mechanically wounded. Remarkably, only Pvpgip4 appeared to be moderately induced by mechanical wounding. These results provide evidence that endopolygalacturonases contribute to the infection process during host colonization by promoting the release of plant cell oligogalacturonides, which are powerful signaling molecules and may also activate plant defenses, such as polygaiacturonase-inhibiting proteins.</abstract><doi>10.4238/vol9-2gmr776</doi><tpages>11</tpages></addata></record> |
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subjects | Beans Colonization Endopolygalacturonase Host plants Infection oligogalacturonides pgip gene Phaseolus vulgaris Plant cells Polymerase chain reaction Reverse transcription Sclerotinia sclerotiorum Stems Transcription Wounding |
title | Characterization of the dry bean polygaiacturonase-inhibiting protein (PGIP) gene family during Sclerotinia sclerotiorum (Sderotiniaceae) infection |
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