Disrupted nitric oxide homeostasis impacts fertility through multiple processes including protein quality control
Plant fertility is fundamental to plant survival and requires the coordinated interaction of developmental pathways and signaling molecules. Nitric oxide (NO) is a small, gaseous signaling molecule that plays crucial roles in plant fertility as well as other developmental processes and stress respon...
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description | Plant fertility is fundamental to plant survival and requires the coordinated interaction of developmental pathways and signaling molecules. Nitric oxide (NO) is a small, gaseous signaling molecule that plays crucial roles in plant fertility as well as other developmental processes and stress responses. NO influences biological processes through S-nitrosation, the posttranslational modification of protein cysteines to S-nitrosocysteine (R-SNO). NO homeostasis is controlled by S-nitrosoglutathione reductase (GSNOR), which reduces S-nitrosoglutathione (GSNO), the major form of NO in cells. GSNOR mutants (hot5-2/gsnor1) have defects in female gametophyte development along with elevated levels of reactive nitrogen species and R-SNOs. To better understand the fertility defects in hot5-2, we investigated the in vivo nitrosoproteome of Arabidopsis (Arabidopsis thaliana) floral tissues coupled with quantitative proteomics of pistils. To identify protein-SNOs, we used an organomercury-based method that involves direct reaction with S-nitrosocysteine, enabling specific identification of S-nitrosocysteine-containing peptides and S-nitrosated proteins. We identified 1,102 endogenously S-nitrosated proteins in floral tissues, of which 1,049 were unique to hot5-2. Among the identified proteins, 728 were novel S-nitrosation targets. Notably, specific UDP-glycosyltransferases and argonaute proteins are S-nitrosated in floral tissues and differentially regulated in pistils. We also discovered S-nitrosation of subunits of the 26S proteasome together with increased abundance of proteasomal components and enhanced trypsin-like proteasomal activity in hot5-2 pistils. Our data establish a method for nitrosoprotein detection in plants, expand knowledge of the plant S-nitrosoproteome, and suggest that nitro-oxidative modification and NO homeostasis are critical to protein quality control in reproductive tissues. |
doi_str_mv | 10.1093/plphys/kiae609 |
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Nitric oxide (NO) is a small, gaseous signaling molecule that plays crucial roles in plant fertility as well as other developmental processes and stress responses. NO influences biological processes through S-nitrosation, the posttranslational modification of protein cysteines to S-nitrosocysteine (R-SNO). NO homeostasis is controlled by S-nitrosoglutathione reductase (GSNOR), which reduces S-nitrosoglutathione (GSNO), the major form of NO in cells. GSNOR mutants (hot5-2/gsnor1) have defects in female gametophyte development along with elevated levels of reactive nitrogen species and R-SNOs. To better understand the fertility defects in hot5-2, we investigated the in vivo nitrosoproteome of Arabidopsis (Arabidopsis thaliana) floral tissues coupled with quantitative proteomics of pistils. To identify protein-SNOs, we used an organomercury-based method that involves direct reaction with S-nitrosocysteine, enabling specific identification of S-nitrosocysteine-containing peptides and S-nitrosated proteins. We identified 1,102 endogenously S-nitrosated proteins in floral tissues, of which 1,049 were unique to hot5-2. Among the identified proteins, 728 were novel S-nitrosation targets. Notably, specific UDP-glycosyltransferases and argonaute proteins are S-nitrosated in floral tissues and differentially regulated in pistils. We also discovered S-nitrosation of subunits of the 26S proteasome together with increased abundance of proteasomal components and enhanced trypsin-like proteasomal activity in hot5-2 pistils. Our data establish a method for nitrosoprotein detection in plants, expand knowledge of the plant S-nitrosoproteome, and suggest that nitro-oxidative modification and NO homeostasis are critical to protein quality control in reproductive tissues.</description><identifier>ISSN: 0032-0889</identifier><identifier>ISSN: 1532-2548</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1093/plphys/kiae609</identifier><identifier>PMID: 39522168</identifier><language>eng</language><publisher>United States</publisher><subject>Aldehyde Oxidoreductases - genetics ; Aldehyde Oxidoreductases - metabolism ; Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis - physiology ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Cysteine - analogs & derivatives ; Fertility ; Flowers - genetics ; Flowers - metabolism ; Glutathione Reductase ; Homeostasis ; Mutation - genetics ; Nitric Oxide - metabolism ; Proteasome Endopeptidase Complex - metabolism ; Proteomics - methods ; S-Nitrosothiols - metabolism</subject><ispartof>Plant physiology (Bethesda), 2024-12, Vol.197 (1)</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of American Society of Plant Biologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c220t-766fb029f6a83732658981c0c1eb29d34d788fd55b9845ca1da47d5843c19efb3</cites><orcidid>0000-0003-1720-5523 ; 0000-0002-0066-4881</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39522168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Treffon, Patrick</creatorcontrib><creatorcontrib>Vierling, Elizabeth</creatorcontrib><title>Disrupted nitric oxide homeostasis impacts fertility through multiple processes including protein quality control</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>Plant fertility is fundamental to plant survival and requires the coordinated interaction of developmental pathways and signaling molecules. Nitric oxide (NO) is a small, gaseous signaling molecule that plays crucial roles in plant fertility as well as other developmental processes and stress responses. NO influences biological processes through S-nitrosation, the posttranslational modification of protein cysteines to S-nitrosocysteine (R-SNO). NO homeostasis is controlled by S-nitrosoglutathione reductase (GSNOR), which reduces S-nitrosoglutathione (GSNO), the major form of NO in cells. GSNOR mutants (hot5-2/gsnor1) have defects in female gametophyte development along with elevated levels of reactive nitrogen species and R-SNOs. To better understand the fertility defects in hot5-2, we investigated the in vivo nitrosoproteome of Arabidopsis (Arabidopsis thaliana) floral tissues coupled with quantitative proteomics of pistils. To identify protein-SNOs, we used an organomercury-based method that involves direct reaction with S-nitrosocysteine, enabling specific identification of S-nitrosocysteine-containing peptides and S-nitrosated proteins. We identified 1,102 endogenously S-nitrosated proteins in floral tissues, of which 1,049 were unique to hot5-2. Among the identified proteins, 728 were novel S-nitrosation targets. Notably, specific UDP-glycosyltransferases and argonaute proteins are S-nitrosated in floral tissues and differentially regulated in pistils. We also discovered S-nitrosation of subunits of the 26S proteasome together with increased abundance of proteasomal components and enhanced trypsin-like proteasomal activity in hot5-2 pistils. Our data establish a method for nitrosoprotein detection in plants, expand knowledge of the plant S-nitrosoproteome, and suggest that nitro-oxidative modification and NO homeostasis are critical to protein quality control in reproductive tissues.</description><subject>Aldehyde Oxidoreductases - genetics</subject><subject>Aldehyde Oxidoreductases - metabolism</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis - physiology</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Cysteine - analogs & derivatives</subject><subject>Fertility</subject><subject>Flowers - genetics</subject><subject>Flowers - metabolism</subject><subject>Glutathione Reductase</subject><subject>Homeostasis</subject><subject>Mutation - genetics</subject><subject>Nitric Oxide - metabolism</subject><subject>Proteasome Endopeptidase Complex - metabolism</subject><subject>Proteomics - methods</subject><subject>S-Nitrosothiols - metabolism</subject><issn>0032-0889</issn><issn>1532-2548</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kLtPwzAQhy0EoqWwMiKPLKV-5GGPqDylSiwwR459aQ1OnNqORP97UlpY7k6n73c6fQhdU3JHieSL3vWbXVx8WQUFkSdoSnPO5izPxCmaEjLORAg5QRcxfhJCKKfZOZpwmTNGCzFF2wcbw9AnMLizKViN_bc1gDe-BR-TijZi2_ZKp4gbCMk6m3Y4bYIf1hvcDi7Z3gHug9cQI4xwp91gbLfe7xLYDm8H9RvSvkvBu0t01igX4erYZ-jj6fF9-TJfvT2_Lu9Xc80YSfOyKJqaMNkUSvCSsyIXUlBNNIWaScMzUwrRmDyvpchyrahRWWlykXFNJTQ1n6Hbw93xj-0AMVWtjRqcUx34IVacMlFm5VhH9O6A6uBjDNBUfbCtCruKkmqvuTporo6ax8DN8fZQt2D-8T-v_AcTxX7p</recordid><startdate>20241223</startdate><enddate>20241223</enddate><creator>Treffon, Patrick</creator><creator>Vierling, Elizabeth</creator><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><orcidid>https://orcid.org/0000-0003-1720-5523</orcidid><orcidid>https://orcid.org/0000-0002-0066-4881</orcidid></search><sort><creationdate>20241223</creationdate><title>Disrupted nitric oxide homeostasis impacts fertility through multiple processes including protein quality control</title><author>Treffon, Patrick ; Vierling, Elizabeth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c220t-766fb029f6a83732658981c0c1eb29d34d788fd55b9845ca1da47d5843c19efb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aldehyde Oxidoreductases - genetics</topic><topic>Aldehyde Oxidoreductases - metabolism</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis - physiology</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Cysteine - analogs & derivatives</topic><topic>Fertility</topic><topic>Flowers - genetics</topic><topic>Flowers - metabolism</topic><topic>Glutathione Reductase</topic><topic>Homeostasis</topic><topic>Mutation - genetics</topic><topic>Nitric Oxide - metabolism</topic><topic>Proteasome Endopeptidase Complex - metabolism</topic><topic>Proteomics - methods</topic><topic>S-Nitrosothiols - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Treffon, Patrick</creatorcontrib><creatorcontrib>Vierling, Elizabeth</creatorcontrib><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><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Treffon, Patrick</au><au>Vierling, Elizabeth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Disrupted nitric oxide homeostasis impacts fertility through multiple processes including protein quality control</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2024-12-23</date><risdate>2024</risdate><volume>197</volume><issue>1</issue><issn>0032-0889</issn><issn>1532-2548</issn><eissn>1532-2548</eissn><abstract>Plant fertility is fundamental to plant survival and requires the coordinated interaction of developmental pathways and signaling molecules. Nitric oxide (NO) is a small, gaseous signaling molecule that plays crucial roles in plant fertility as well as other developmental processes and stress responses. NO influences biological processes through S-nitrosation, the posttranslational modification of protein cysteines to S-nitrosocysteine (R-SNO). NO homeostasis is controlled by S-nitrosoglutathione reductase (GSNOR), which reduces S-nitrosoglutathione (GSNO), the major form of NO in cells. GSNOR mutants (hot5-2/gsnor1) have defects in female gametophyte development along with elevated levels of reactive nitrogen species and R-SNOs. To better understand the fertility defects in hot5-2, we investigated the in vivo nitrosoproteome of Arabidopsis (Arabidopsis thaliana) floral tissues coupled with quantitative proteomics of pistils. To identify protein-SNOs, we used an organomercury-based method that involves direct reaction with S-nitrosocysteine, enabling specific identification of S-nitrosocysteine-containing peptides and S-nitrosated proteins. We identified 1,102 endogenously S-nitrosated proteins in floral tissues, of which 1,049 were unique to hot5-2. Among the identified proteins, 728 were novel S-nitrosation targets. Notably, specific UDP-glycosyltransferases and argonaute proteins are S-nitrosated in floral tissues and differentially regulated in pistils. We also discovered S-nitrosation of subunits of the 26S proteasome together with increased abundance of proteasomal components and enhanced trypsin-like proteasomal activity in hot5-2 pistils. Our data establish a method for nitrosoprotein detection in plants, expand knowledge of the plant S-nitrosoproteome, and suggest that nitro-oxidative modification and NO homeostasis are critical to protein quality control in reproductive tissues.</abstract><cop>United States</cop><pmid>39522168</pmid><doi>10.1093/plphys/kiae609</doi><orcidid>https://orcid.org/0000-0003-1720-5523</orcidid><orcidid>https://orcid.org/0000-0002-0066-4881</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aldehyde Oxidoreductases - genetics Aldehyde Oxidoreductases - metabolism Arabidopsis - genetics Arabidopsis - metabolism Arabidopsis - physiology Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Cysteine - analogs & derivatives Fertility Flowers - genetics Flowers - metabolism Glutathione Reductase Homeostasis Mutation - genetics Nitric Oxide - metabolism Proteasome Endopeptidase Complex - metabolism Proteomics - methods S-Nitrosothiols - metabolism |
title | Disrupted nitric oxide homeostasis impacts fertility through multiple processes including protein quality control |
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