Analysis of the Arabidopsis Floral Proteome: Detection of over 2 000 Proteins and Evidence for Posttranslational Modifications
The proteome of the Arabidopsis flower has not been extensively studied previously. Here, we report a proteomic analysis of the wild type Arabidopsis flower. Using both two-dimensional electrophoresis/mass spectrometry (2-DGE/MS) and multi-dimensional protein identification technology (MudPIT) appro...
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description | The proteome of the Arabidopsis flower has not been extensively studied previously. Here, we report a proteomic analysis of the wild type Arabidopsis flower. Using both two-dimensional electrophoresis/mass spectrometry (2-DGE/MS) and multi-dimensional protein identification technology (MudPIT) approaches, we identified 2 446 proteins. Although a single experiment or analysis uncovered only a subset of the proteins we identified, a combination of multiple experiments and analyses facilitated the detection of a greater number of proteins. When proteins are grouped according to RNA expression levels revealed by microarray experiments, we found that proteins encoded by genes with relatively high levels of expression were detected with greater frequencies. On the other hand, at the level of the individual gene/protein, there was not a good correlation between protein spot intensity and microarray values. We also obtained strong evidence for post-translational modification from 2-DGE and MudPIT data. We detected proteins that are annotated to function in protein synthesis, folding, modification, and degradation, as well as the presence of regulatory proteins such as transcription factors and protein kinases. Finally, sequence and evolutionary analysis of genes for active methyl group metabolisms suggests that these genes are highly conserved. Our results allow the formulation of hypotheses regarding post-translational regulation of proteins in the flower, providing new understanding about Arabidopsis flower development and physiology. |
doi_str_mv | 10.1111/j.1744-7909.2008.00787.x |
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Here, we report a proteomic analysis of the wild type Arabidopsis flower. Using both two-dimensional electrophoresis/mass spectrometry (2-DGE/MS) and multi-dimensional protein identification technology (MudPIT) approaches, we identified 2 446 proteins. Although a single experiment or analysis uncovered only a subset of the proteins we identified, a combination of multiple experiments and analyses facilitated the detection of a greater number of proteins. When proteins are grouped according to RNA expression levels revealed by microarray experiments, we found that proteins encoded by genes with relatively high levels of expression were detected with greater frequencies. On the other hand, at the level of the individual gene/protein, there was not a good correlation between protein spot intensity and microarray values. We also obtained strong evidence for post-translational modification from 2-DGE and MudPIT data. We detected proteins that are annotated to function in protein synthesis, folding, modification, and degradation, as well as the presence of regulatory proteins such as transcription factors and protein kinases. Finally, sequence and evolutionary analysis of genes for active methyl group metabolisms suggests that these genes are highly conserved. Our results allow the formulation of hypotheses regarding post-translational regulation of proteins in the flower, providing new understanding about Arabidopsis flower development and physiology.</description><identifier>ISSN: 1672-9072</identifier><identifier>EISSN: 1744-7909</identifier><identifier>DOI: 10.1111/j.1744-7909.2008.00787.x</identifier><identifier>PMID: 19200160</identifier><language>eng</language><publisher>Melbourne, Australia: Melbourne, Australia : Blackwell Publishing Asia</publisher><subject>Arabidopsis ; Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis Proteins - metabolism ; Computational Biology ; Electrophoresis, Gel, Two-Dimensional ; floral ; Flowers - metabolism ; Mass Spectrometry ; Methylation ; multi-dimensional protein identification technology ; Phylogeny ; protein modification ; Protein Processing, Post-Translational ; Proteome ; RNA, Messenger - metabolism ; S-Adenosylmethionine - biosynthesis</subject><ispartof>Journal of integrative plant biology, 2009-02, Vol.51 (2), p.207-223</ispartof><rights>2009 Institute of Botany, the Chinese Academy of Sciences</rights><rights>Copyright © Wanfang Data Co. 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All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3897-99a787581f53bc85ae23bccee5d0f637bc8a959bdcb8e33f31e0a5ad6db77e423</citedby><cites>FETCH-LOGICAL-c3897-99a787581f53bc85ae23bccee5d0f637bc8a959bdcb8e33f31e0a5ad6db77e423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/zwxb/zwxb.jpg</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1744-7909.2008.00787.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1744-7909.2008.00787.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19200160$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Baomin</creatorcontrib><creatorcontrib>Li, Lianchao</creatorcontrib><creatorcontrib>Zhou, Xiaofan</creatorcontrib><creatorcontrib>Stanley, Bruce</creatorcontrib><creatorcontrib>Ma, Hong</creatorcontrib><title>Analysis of the Arabidopsis Floral Proteome: Detection of over 2 000 Proteins and Evidence for Posttranslational Modifications</title><title>Journal of integrative plant biology</title><addtitle>J Integr Plant Biol</addtitle><description>The proteome of the Arabidopsis flower has not been extensively studied previously. Here, we report a proteomic analysis of the wild type Arabidopsis flower. Using both two-dimensional electrophoresis/mass spectrometry (2-DGE/MS) and multi-dimensional protein identification technology (MudPIT) approaches, we identified 2 446 proteins. Although a single experiment or analysis uncovered only a subset of the proteins we identified, a combination of multiple experiments and analyses facilitated the detection of a greater number of proteins. When proteins are grouped according to RNA expression levels revealed by microarray experiments, we found that proteins encoded by genes with relatively high levels of expression were detected with greater frequencies. On the other hand, at the level of the individual gene/protein, there was not a good correlation between protein spot intensity and microarray values. We also obtained strong evidence for post-translational modification from 2-DGE and MudPIT data. We detected proteins that are annotated to function in protein synthesis, folding, modification, and degradation, as well as the presence of regulatory proteins such as transcription factors and protein kinases. Finally, sequence and evolutionary analysis of genes for active methyl group metabolisms suggests that these genes are highly conserved. Our results allow the formulation of hypotheses regarding post-translational regulation of proteins in the flower, providing new understanding about Arabidopsis flower development and physiology.</description><subject>Arabidopsis</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Computational Biology</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>floral</subject><subject>Flowers - metabolism</subject><subject>Mass Spectrometry</subject><subject>Methylation</subject><subject>multi-dimensional protein identification technology</subject><subject>Phylogeny</subject><subject>protein modification</subject><subject>Protein Processing, Post-Translational</subject><subject>Proteome</subject><subject>RNA, Messenger - metabolism</subject><subject>S-Adenosylmethionine - biosynthesis</subject><issn>1672-9072</issn><issn>1744-7909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFy0zAQhj0MDC2FVwBd6M1hZdmWxAyHtDSlTAOZKR1608j2qig4VpCcNuHAsyPXmXJFl12tvn-10p8khMKExvVuOaE8z1MuQU4yADEB4IJPtk-Sw8eDpzEveZZK4NlB8iKEJQATUGbPkwMqo4qWcJj8mXa63QUbiDOk_4Fk6nVlG7ceSrPWed2ShXc9uhW-Jx-xx7q3rhtod4eeZAQARsJ2geiuIWd3tsGuRmKcJwsX-t7rLrR60MVuc9dYY-uHbXiZPDO6DfhqH4-S69nZt9NP6eXX84vT6WVaMyF5KqWO7ysENQWralFozGKsEYsGTMl4rGlZyKqpK4GMGUYRdKGbsqk4xzxjR8nbse-97ozubtXSbXycJqjf99sqfoaEDOjAHY_c2rtfGwy9WtlQY9vqDt0mqLIUUpY0j6AYwdq7EDwatfZ2pf1OUVCDR2qpBivUYIUaPFIPHqltlL7e37GpVtj8E-5NicCH_bC2xd1_N1afLxYnMYv6dNTb0OP2Ua_9T1Vyxgv1_cu5urqZz25OxFwVkX8z8kY7pW-9Der6Kn4HA1qInPOM_QVoz7mT</recordid><startdate>200902</startdate><enddate>200902</enddate><creator>Feng, Baomin</creator><creator>Li, Lianchao</creator><creator>Zhou, Xiaofan</creator><creator>Stanley, Bruce</creator><creator>Ma, Hong</creator><general>Melbourne, Australia : Blackwell Publishing Asia</general><general>Blackwell Publishing Asia</general><general>Department of Biology, the Pennsylvania State University, University Park, PA 16802, USA%proteomics and Mass Spectrometry Core Facility, 003 Althouse Laboratory, the Pennsylvania State University, University Park, PA 16802, USA%The Intercollege Graduate Program in Cell and Developmental Biology, the Huck Institutes of the Life Sciences, the Pennsylvania State University,University Park, PA 16802, USA%Section of Research Resources H093, the College of Medicine, the Pennsylvania State University, Hershey, PA 17033, USA</general><scope>FBQ</scope><scope>BSCLL</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>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>200902</creationdate><title>Analysis of the Arabidopsis Floral Proteome: Detection of over 2 000 Proteins and Evidence for Posttranslational Modifications</title><author>Feng, Baomin ; Li, Lianchao ; Zhou, Xiaofan ; Stanley, Bruce ; Ma, Hong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3897-99a787581f53bc85ae23bccee5d0f637bc8a959bdcb8e33f31e0a5ad6db77e423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Arabidopsis</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Computational Biology</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>floral</topic><topic>Flowers - metabolism</topic><topic>Mass Spectrometry</topic><topic>Methylation</topic><topic>multi-dimensional protein identification technology</topic><topic>Phylogeny</topic><topic>protein modification</topic><topic>Protein Processing, Post-Translational</topic><topic>Proteome</topic><topic>RNA, Messenger - metabolism</topic><topic>S-Adenosylmethionine - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Baomin</creatorcontrib><creatorcontrib>Li, Lianchao</creatorcontrib><creatorcontrib>Zhou, Xiaofan</creatorcontrib><creatorcontrib>Stanley, Bruce</creatorcontrib><creatorcontrib>Ma, Hong</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Journal of integrative plant biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Baomin</au><au>Li, Lianchao</au><au>Zhou, Xiaofan</au><au>Stanley, Bruce</au><au>Ma, Hong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of the Arabidopsis Floral Proteome: Detection of over 2 000 Proteins and Evidence for Posttranslational Modifications</atitle><jtitle>Journal of integrative plant biology</jtitle><addtitle>J Integr Plant Biol</addtitle><date>2009-02</date><risdate>2009</risdate><volume>51</volume><issue>2</issue><spage>207</spage><epage>223</epage><pages>207-223</pages><issn>1672-9072</issn><eissn>1744-7909</eissn><abstract>The proteome of the Arabidopsis flower has not been extensively studied previously. Here, we report a proteomic analysis of the wild type Arabidopsis flower. Using both two-dimensional electrophoresis/mass spectrometry (2-DGE/MS) and multi-dimensional protein identification technology (MudPIT) approaches, we identified 2 446 proteins. Although a single experiment or analysis uncovered only a subset of the proteins we identified, a combination of multiple experiments and analyses facilitated the detection of a greater number of proteins. When proteins are grouped according to RNA expression levels revealed by microarray experiments, we found that proteins encoded by genes with relatively high levels of expression were detected with greater frequencies. On the other hand, at the level of the individual gene/protein, there was not a good correlation between protein spot intensity and microarray values. We also obtained strong evidence for post-translational modification from 2-DGE and MudPIT data. We detected proteins that are annotated to function in protein synthesis, folding, modification, and degradation, as well as the presence of regulatory proteins such as transcription factors and protein kinases. Finally, sequence and evolutionary analysis of genes for active methyl group metabolisms suggests that these genes are highly conserved. Our results allow the formulation of hypotheses regarding post-translational regulation of proteins in the flower, providing new understanding about Arabidopsis flower development and physiology.</abstract><cop>Melbourne, Australia</cop><pub>Melbourne, Australia : Blackwell Publishing Asia</pub><pmid>19200160</pmid><doi>10.1111/j.1744-7909.2008.00787.x</doi><tpages>17</tpages></addata></record> |
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subjects | Arabidopsis Arabidopsis - genetics Arabidopsis - metabolism Arabidopsis Proteins - metabolism Computational Biology Electrophoresis, Gel, Two-Dimensional floral Flowers - metabolism Mass Spectrometry Methylation multi-dimensional protein identification technology Phylogeny protein modification Protein Processing, Post-Translational Proteome RNA, Messenger - metabolism S-Adenosylmethionine - biosynthesis |
title | Analysis of the Arabidopsis Floral Proteome: Detection of over 2 000 Proteins and Evidence for Posttranslational Modifications |
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