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The Plant Cell was founded on four key tenets: (1) to publish the most exciting, cutting-edge research in plant cellular and molecular biology, (2) to provide the most rapid turnaround time possible for reviewing and publishing a research paper, (3) to feature the highest quality reproduction of data, and (4) to provide, in the front section of the journal, a more interactive format for commentaries, opinion pieces, and the exchange of information and ideas in review articles, meeting reports, and insightful overviews of featured research papers.","PUBLISHER","PENDING",null,0,[27,33],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":29,"label":30,"description":32,"parentId":24,"standard":24,"scholarHubFieldId":24},"ac5e8493-1d6c-4151-82cf-2a41e5c3f89d",[],{"EN":31},"Plant Science",{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":35,"label":36,"description":38,"parentId":24,"standard":24,"scholarHubFieldId":24},"131e254e-0b02-478f-aa3e-0b27d8c7b9d1",[],{"EN":37},"Cell Biology",{},[40,47],{"id":41,"createTime":24,"updateTime":24,"relativeEntities":42,"slug":24,"properties":43,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":46,"statistic":24},"3b2b3c1e-d793-4160-89dd-eb4e42b70e4a",[],{"title":44},{"EN":45},"Oxford University Press",[],{"id":48,"createTime":24,"updateTime":24,"relativeEntities":49,"slug":24,"properties":50,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":53,"statistic":24},"d2632cba-5e0e-467d-8e4d-1af4354a667b",[],{"title":51},{"EN":52},"OXFORD UNIV PRESS INC",[],[55,73],{"id":56,"indexDatabase":57,"url":67,"indexYears":68,"academicFieldIds":69,"indexDatabaseRanking":72},"cc6f5156-a6ed-47f8-aeaf-0ff277f9b38a",{"id":58,"createTime":24,"updateTime":24,"relativeEntities":59,"label":60,"description":62,"key":64,"publicationTags":65,"standard":24},"3c7051d4-eb7d-4c57-a56b-36fc74c5d1e9",[],{"EN":61,"VI":61},"Scopus - Elsevier",{"EN":61,"VI":63},"Cơ sở dữ liệu Scopus thuộc Elsevier","scopus",[66],"SCOPUS","https:\u002F\u002Fwww.scopus.com\u002Fsourceid\u002F16594","1989-2025",[70,71],"0a123226-342a-4226-9f31-dbd65f4aaf4b","d2139bd1-2fdb-481b-a416-9c30dd0cc173","SCOPUS__Q1",{"id":74,"indexDatabase":75,"url":87,"indexYears":24,"academicFieldIds":88,"indexDatabaseRanking":24},"4705c8f8-c3ba-480e-a58f-33cf68f6f626",{"id":76,"createTime":24,"updateTime":24,"relativeEntities":77,"label":78,"description":80,"key":83,"publicationTags":84,"standard":24},"a4921856-b128-4d9f-8f1f-e80813d3bbd4",[],{"EN":79,"VI":79},"ISI\u002FSCIE - Science Citation Index Expanded",{"EN":81,"VI":82},"SCIE database","Cơ sở dữ liệu SCIE","scie",[85,86],"SCIE","ISI","https:\u002F\u002Fmjl.clarivate.com\u002Fsearch-results?issn=1040-4651",[89,90,91],"10e9c71e-2256-419c-bdd2-a39e436e76e3","358d4f60-a926-4ec8-965c-590255430c86","8eb75d88-0c7a-497c-a346-e729afc75040","http:\u002F\u002Fwww.plantcell.org\u002F",{"meta":94,"data":96},{"total":95},"393",[97,495,1141,1581,1921,2034,2204,2338,2687,3144],{"id":98,"createTime":99,"updateTime":100,"relativeEntities":101,"slug":102,"properties":103,"entityType":120,"verifyStatus":121,"verifyTime":122,"verifyNote":123,"languages":124,"translateLanguages":24,"viewCount":25,"primaryUrl":126,"fullTextUrl":24,"authors":127,"publicationType":177,"publisherRelationship":178,"citationCount":228,"citationInfo":229,"publishDate":253,"publishYear":230,"citationAnalyzeStatus":254,"lastCitationAnalyze":100,"indexDatabases":255,"openAccess":24,"references":256,"isForceReanalyzing":494},"bfbfbf02-675d-468f-8157-c00705344fdc","2024-10-05T18:07:23.457+00:00","2026-07-26T17:57:58.759+00:00",[],"Antiquity-of-MicroRNAs-and-Their-Targets-in-Land-Plants",{"mag":104,"gsPaper":106,"pmc":108,"openalex":110,"abstract":112,"title":114,"pm":116,"doi":118},{"VOID":105},"2123687559",{"VOID":107},"[\"9640644653505682634\"]",{"VOID":109},"1143068",{"VOID":111},"W2123687559",{"EN":113},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>MicroRNAs (miRNAs) affect the morphology of flowering plants by the posttranscriptional regulation of genes involved in critical developmental events. Understanding the spatial and temporal dynamics of miRNA activity during development is therefore central for understanding miRNA functions. We describe a microarray suitable for detection of plant miRNAs. Profiling of Arabidopsis thaliana miRNAs during normal development extends previous expression analyses, highlighting differential expression of miRNA families within specific organs and tissue types. Comparison of our miRNA expression data with existing mRNA microarray data provided a global intersection of plant miRNA and mRNA expression profiles and revealed that tissues in which a given miRNA is highly expressed are unlikely to also show high expression of the corresponding targets. Expression profiling was also used in a phylogenetic survey to test the depth of plant miRNA conservation. Of the 23 families of miRNAs tested, expression of 11 was detected in a gymnosperm and eight in a fern, directly demonstrating that many plant miRNAs have remained essentially unchanged since before the emergence of flowering plants. We also describe an empirical strategy for detecting miRNA target genes from unsequenced transcriptomes and show that targets in nonflowering plants as deeply branching as ferns and mosses are homologous to the targets in Arabidopsis. Therefore, several individual miRNA regulatory circuits have ancient origins and have remained intact throughout the evolution and diversification of plants.\u003C\u002Fjats:p>",{"EN":115},"Antiquity of MicroRNAs and Their Targets in Land Plants",{"VOID":117},"15849273",{"VOID":119},"10.1105\u002Ftpc.105.032185","PUBLICATION","VERIFIED","2024-10-05T18:07:23.456+00:00","Auto Verify",[125],"EN","https:\u002F\u002Facademic.oup.com\u002Fplcell\u002Farticle\u002F17\u002F6\u002F1658\u002F6114539",[128,149],{"id":129,"sortIndex":25,"researcher":24,"roles":130,"affiliations":131,"properties":140,"displayName":144,"givenName":24,"familyName":24},"c3f3f620-8143-4185-b24e-bc36ce2d8379",[],[132],{"id":133,"sortIndex":25,"affiliation":134,"properties":24},"7c7d1bfa-542f-42ea-a159-abffd048d918",{"id":133,"createTime":24,"updateTime":24,"relativeEntities":135,"slug":24,"properties":136,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":139,"statistic":24},[],{"title":137},{"EN":138},"aWhitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142",[],{"orcid":141,"title":143,"gsAuthor":145,"openalex":147},{"VOID":142},"https:\u002F\u002Forcid.org\u002F0000-0001-8951-7361",{"EN":144},"Michael J. 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Genet., 36, 1282, 10.1038\u002Fng1478",{"doi":268},"10.1038\u002Fng1478",{"id":24,"text":270,"url":24,"identifiers":271},"2004, Nature, 431, 350, 10.1038\u002Fnature02871",{"doi":272},"10.1038\u002Fnature02871",{"id":24,"text":274,"url":24,"identifiers":275},"2003, Plant Cell, 15, 2730, 10.1105\u002Ftpc.016238",{"doi":276},"10.1105\u002Ftpc.016238",{"id":24,"text":278,"url":24,"identifiers":279},"2004, RNA, 10, 1813, 10.1261\u002Frna.7119904",{"doi":280},"10.1261\u002Frna.7119904",{"id":24,"text":282,"url":24,"identifiers":283},"2005, Curr Biol, 15, 303, 10.1016\u002Fj.cub.2005.02.017",{"doi":284},"10.1016\u002Fj.cub.2005.02.017",{"id":24,"text":286,"url":24,"identifiers":287},"2004, Cell, 116, 281, 10.1016\u002FS0092-8674(04)00045-5",{"doi":288},"10.1016\u002FS0092-8674(04)00045-5",{"id":24,"text":290,"url":24,"identifiers":291},"2005, RNA, 11, 241, 10.1261\u002Frna.7240905",{"doi":292},"10.1261\u002Frna.7240905",{"id":24,"text":294,"url":24,"identifiers":295},"2004, Proc. Natl. Acad. Sci. USA, 101, 11511, 10.1073\u002Fpnas.0404025101",{"doi":296},"10.1073\u002Fpnas.0404025101",{"id":24,"text":298,"url":24,"identifiers":299},"2003, Cell, 113, 25, 10.1016\u002FS0092-8674(03)00231-9",{"doi":300},"10.1016\u002FS0092-8674(03)00231-9",{"id":24,"text":302,"url":24,"identifiers":303},"1986, Proc. Natl. Acad. Sci. USA, 83, 3746, 10.1073\u002Fpnas.83.11.3746",{"doi":304},"10.1073\u002Fpnas.83.11.3746",{"id":24,"text":306,"url":24,"identifiers":307},"2003",{},{"id":24,"text":309,"url":24,"identifiers":310},"1993, Plant Mol. Biol. Rep., 11, 113, 10.1007\u002FBF02670468",{"doi":311},"10.1007\u002FBF02670468",{"id":24,"text":313,"url":24,"identifiers":314},"2004, Science, 303, 2022, 10.1126\u002Fscience.1088060",{"doi":315},"10.1126\u002Fscience.1088060",{"id":24,"text":317,"url":24,"identifiers":318},"2004, Curr. Opin. Plant Biol., 7, 512, 10.1016\u002Fj.pbi.2004.07.011",{"doi":319},"10.1016\u002Fj.pbi.2004.07.011",{"id":24,"text":321,"url":24,"identifiers":322},"2003, Curr. Biol., 13, 1768, 10.1016\u002Fj.cub.2003.09.035",{"doi":323},"10.1016\u002Fj.cub.2003.09.035",{"id":24,"text":325,"url":24,"identifiers":326},"2004, Nature, 428, 485, 10.1038\u002F428485a",{"doi":327},"10.1038\u002F428485a",{"id":24,"text":329,"url":24,"identifiers":330},"2005, Nucleic Acids Res., 33D, D637",{},{"id":24,"text":332,"url":24,"identifiers":333},"2004, Mol. Cell, 14, 787, 10.1016\u002Fj.molcel.2004.05.027",{"doi":334},"10.1016\u002Fj.molcel.2004.05.027",{"id":24,"text":336,"url":24,"identifiers":337},"2004, Nature, 428, 84, 10.1038\u002Fnature02363",{"doi":338},"10.1038\u002Fnature02363",{"id":24,"text":340,"url":24,"identifiers":341},"2003, Dev. Cell, 4, 205, 10.1016\u002FS1534-5807(03)00025-X",{"doi":342},"10.1016\u002FS1534-5807(03)00025-X",{"id":24,"text":344,"url":24,"identifiers":345},"2004, Nature, 428, 81, 10.1038\u002Fnature02366",{"doi":346},"10.1038\u002Fnature02366",{"id":24,"text":348,"url":24,"identifiers":349},"2005, Plant J., 42, 84, 10.1111\u002Fj.1365-313X.2005.02354.x",{"doi":350},"10.1111\u002Fj.1365-313X.2005.02354.x",{"id":24,"text":352,"url":24,"identifiers":353},"2003, RNA, 9, 1274, 10.1261\u002Frna.5980303",{"doi":354},"10.1261\u002Frna.5980303",{"id":24,"text":356,"url":24,"identifiers":357},"2001, Science, 294, 858, 10.1126\u002Fscience.1065062",{"doi":358},"10.1126\u002Fscience.1065062",{"id":24,"text":360,"url":24,"identifiers":361},"2004, Development, 131, 4311, 10.1242\u002Fdev.01320",{"doi":362},"10.1242\u002Fdev.01320",{"id":24,"text":364,"url":24,"identifiers":365},"2005, Nucleic Acids Res., 33, e17, 10.1093\u002Fnar\u002Fgni019",{"doi":366},"10.1093\u002Fnar\u002Fgni019",{"id":24,"text":368,"url":24,"identifiers":369},"2005, Nature, 433, 769, 10.1038\u002Fnature03315",{"doi":370},"10.1038\u002Fnature03315",{"id":24,"text":372,"url":24,"identifiers":373},"2003, Genes Dev., 17, 991, 10.1101\u002Fgad.1074403",{"doi":374},"10.1101\u002Fgad.1074403",{"id":24,"text":376,"url":24,"identifiers":377},"2004, Proc. Natl. Acad. Sci. USA, 101, 9740, 10.1073\u002Fpnas.0403293101",{"doi":378},"10.1073\u002Fpnas.0403293101",{"id":24,"text":380,"url":24,"identifiers":381},"2002, Science, 297, 2053, 10.1126\u002Fscience.1076311",{"doi":382},"10.1126\u002Fscience.1076311",{"id":24,"text":384,"url":24,"identifiers":385},"2005, Plant Cell, 17, 1360, 10.1105\u002Ftpc.105.031716",{"doi":386},"10.1105\u002Ftpc.105.031716",{"id":24,"text":388,"url":24,"identifiers":389},"2004, Curr. Biol., 14, 1035, 10.1016\u002Fj.cub.2004.06.022",{"doi":390},"10.1016\u002Fj.cub.2004.06.022",{"id":24,"text":392,"url":24,"identifiers":393},"2001, Plant Cell, 13, 571, 10.1105\u002Ftpc.13.3.571",{"doi":394},"10.1105\u002Ftpc.13.3.571",{"id":24,"text":396,"url":24,"identifiers":397},"2004, EMBO J., 23, 3356, 10.1038\u002Fsj.emboj.7600340",{"doi":398},"10.1038\u002Fsj.emboj.7600340",{"id":24,"text":400,"url":24,"identifiers":401},"2001, Nature, 411, 709, 10.1038\u002F35079635",{"doi":402},"10.1038\u002F35079635",{"id":24,"text":404,"url":24,"identifiers":405},"2004, Plant Cell, 16, 1730, 10.1105\u002Ftpc.021816",{"doi":406},"10.1105\u002Ftpc.021816",{"id":24,"text":408,"url":24,"identifiers":409},"2005, Plant Cell, 17, 705, 10.1105\u002Ftpc.104.027920",{"doi":410},"10.1105\u002Ftpc.104.027920",{"id":24,"text":412,"url":24,"identifiers":413},"2004, Genome Biol., 5, R68, 10.1186\u002Fgb-2004-5-9-r68",{"doi":414},"10.1186\u002Fgb-2004-5-9-r68",{"id":24,"text":416,"url":24,"identifiers":417},"2004, Nat. 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Biol., 12, 1484, 10.1016\u002FS0960-9822(02)01017-5",{"doi":430},"10.1016\u002FS0960-9822(02)01017-5",{"id":24,"text":432,"url":24,"identifiers":433},"2002, Genes Dev., 16, 1616, 10.1101\u002Fgad.1004402",{"doi":434},"10.1101\u002Fgad.1004402",{"id":24,"text":436,"url":24,"identifiers":437},"2002, Cell, 110, 513, 10.1016\u002FS0092-8674(02)00863-2",{"doi":438},"10.1016\u002FS0092-8674(02)00863-2",{"id":24,"text":440,"url":24,"identifiers":441},"2002, Trends Plant Sci., 7, 487, 10.1016\u002FS1360-1385(02)02355-5",{"doi":442},"10.1016\u002FS1360-1385(02)02355-5",{"id":24,"text":444,"url":24,"identifiers":445},"3, 2005, Nat. Genet., 37",{},{"id":24,"text":447,"url":24,"identifiers":448},"2005, Dev. Cell, 8, 517, 10.1016\u002Fj.devcel.2005.01.018",{"doi":449},"10.1016\u002Fj.devcel.2005.01.018",{"id":24,"text":451,"url":24,"identifiers":452},"2004, Dev. 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Cell, 16, 69, 10.1016\u002Fj.molcel.2004.09.028",{"doi":481},"10.1016\u002Fj.molcel.2004.09.028",{"id":24,"text":483,"url":24,"identifiers":484},"2004, Genome Biol., 5, R65, 10.1186\u002Fgb-2004-5-9-r65",{"doi":485},"10.1186\u002Fgb-2004-5-9-r65",{"id":24,"text":487,"url":24,"identifiers":488},"2004, PLoS Biol, 2, e104, 10.1371\u002Fjournal.pbio.0020104",{"doi":489},"10.1371\u002Fjournal.pbio.0020104",{"id":24,"text":491,"url":24,"identifiers":492},"2004, Plant Cell Physiol., 45, 369, 10.1093\u002Fpcp\u002Fpch051",{"doi":493},"10.1093\u002Fpcp\u002Fpch051",false,{"id":496,"createTime":497,"updateTime":498,"relativeEntities":499,"slug":500,"properties":501,"entityType":120,"verifyStatus":121,"verifyTime":518,"verifyNote":123,"languages":519,"translateLanguages":24,"viewCount":25,"primaryUrl":520,"fullTextUrl":24,"authors":521,"publicationType":177,"publisherRelationship":653,"citationCount":25,"citationInfo":703,"publishDate":706,"publishYear":704,"citationAnalyzeStatus":23,"lastCitationAnalyze":707,"indexDatabases":708,"openAccess":24,"references":709,"isForceReanalyzing":494},"e09141e7-f95a-48ea-808f-a96a2f11ad48","2024-10-16T06:02:58.981+00:00","2026-07-13T19:54:24.112+00:00",[],"In-Depth-Analysis-of-the-Thylakoid-Membrane-Proteome-of-i-Arabidopsis-thaliana-i-Chloroplasts-New-Proteins-New-Functions-and-a-Plastid-Proteome-Database-W-",{"mag":502,"gsPaper":504,"pmc":506,"openalex":508,"abstract":510,"title":512,"pm":514,"doi":516},{"VOID":503},"2147844147",{"VOID":505},"[\"16427689116904256535\"]",{"VOID":507},"341918",{"VOID":509},"W2147844147",{"EN":511},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>An extensive analysis of the Arabidopsis thaliana peripheral and integral thylakoid membrane proteome was performed by sequential extractions with salt, detergent, and organic solvents, followed by multidimensional protein separation steps (reverse-phase HPLC and one- and two-dimensional electrophoresis gels), different enzymatic and nonenzymatic protein cleavage techniques, mass spectrometry, and bioinformatics. Altogether, 154 proteins were identified, of which 76 (49%) were α-helical integral membrane proteins. Twenty-seven new proteins without known function but with predicted chloroplast transit peptides were identified, of which 17 (63%) are integral membrane proteins. These new proteins, likely important in thylakoid biogenesis, include two rubredoxins, a potential metallochaperone, and a new DnaJ-like protein. The data were integrated with our analysis of the lumenal-enriched proteome. We identified 83 out of 100 known proteins of the thylakoid localized photosynthetic apparatus, including several new paralogues and some 20 proteins involved in protein insertion, assembly, folding, or proteolysis. An additional 16 proteins are involved in translation, demonstrating that the thylakoid membrane surface is an important site for protein synthesis. The high coverage of the photosynthetic apparatus and the identification of known hydrophobic proteins with low expression levels, such as cpSecE, Ohp1, and Ohp2, indicate an excellent dynamic resolution of the analysis. The sequential extraction process proved very helpful to validate transmembrane prediction. Our data also were cross-correlated to chloroplast subproteome analyses by other laboratories. All data are deposited in a new curated plastid proteome database (PPDB) with multiple search functions (http:\u002F\u002Fcbsusrv01.tc.cornell.edu\u002Fusers\u002Fppdb\u002F). This PPDB will serve as an expandable resource for the plant community.\u003C\u002Fjats:p>",{"EN":513},"In-Depth Analysis of the Thylakoid Membrane Proteome of\u003Ci>Arabidopsis thaliana\u003C\u002Fi>Chloroplasts: New Proteins, New Functions, and a Plastid Proteome Database[W]",{"VOID":515},"14729914",{"VOID":517},"10.1105\u002Ftpc.017814","2024-10-16T06:02:58.980+00:00",[125],"https:\u002F\u002Facademic.oup.com\u002Fplcell\u002Farticle\u002F16\u002F2\u002F478\u002F6010303",[522,543,562,579,599,615,635],{"id":523,"sortIndex":25,"researcher":24,"roles":524,"affiliations":525,"properties":534,"displayName":538,"givenName":24,"familyName":24},"600d92f0-8c80-4bdb-9f58-d89eecdbd65f",[],[526],{"id":527,"sortIndex":25,"affiliation":528,"properties":24},"a5cfe237-a552-4dac-9848-adaf8e056b67",{"id":527,"createTime":24,"updateTime":24,"relativeEntities":529,"slug":24,"properties":530,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":533,"statistic":24},[],{"title":531},{"VI":532},"Department of Plant Biology, Cornell University, Ithaca, New York 14853",[],{"orcid":535,"title":537,"gsAuthor":539,"openalex":541},{"VOID":536},"https:\u002F\u002Forcid.org\u002F0000-0002-7537-7887",{"EN":538},"Giulia Friso",{"VOID":540},"[\"dx8JKh4AAAAJ\"]",{"VOID":542},"A5046326063",{"id":544,"sortIndex":151,"researcher":24,"roles":545,"affiliations":546,"properties":553,"displayName":557,"givenName":24,"familyName":24},"f2652346-71da-4e53-a20a-57ae38298842",[],[547],{"id":527,"sortIndex":25,"affiliation":548,"properties":24},{"id":527,"createTime":24,"updateTime":24,"relativeEntities":549,"slug":24,"properties":550,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":552,"statistic":24},[],{"title":551},{"VI":532},[],{"orcid":554,"title":556,"gsAuthor":558,"openalex":560},{"VOID":555},"https:\u002F\u002Forcid.org\u002F0000-0002-0697-037X",{"EN":557},"Lisa Giacomelli",{"VOID":559},"[\"zJLI9VoAAAAJ\"]",{"VOID":561},"A5059565731",{"id":563,"sortIndex":252,"researcher":24,"roles":564,"affiliations":565,"properties":572,"displayName":576,"givenName":24,"familyName":24},"0ce72626-9a46-4df3-81f6-6ce7ca431c46",[],[566],{"id":527,"sortIndex":25,"affiliation":567,"properties":24},{"id":527,"createTime":24,"updateTime":24,"relativeEntities":568,"slug":24,"properties":569,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":571,"statistic":24},[],{"title":570},{"VI":532},[],{"orcid":573,"title":575,"openalex":577},{"VOID":574},"https:\u002F\u002Forcid.org\u002F0000-0002-1485-2314",{"EN":576},"A. 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Mol Cell Proteomics  2  ,  325–345.",{"doi":770},"10.1074\u002Fmcp.M300030-MCP200",{"id":24,"text":772,"url":24,"identifiers":773},"Ferro, M., Salvi, D., Riviere-Rolland, H., Vermat, T., Seigneurin-Berny, D., Grunwald, D., Garin, J., Joyard, J., and Rolland, N. (2002). Integral membrane proteins of the chloroplast envelope: Identification and subcellular localization of new transporters. Proc. Natl. Acad. Sci. USA  99  ,  11487–11492.",{"doi":774},"10.1073\u002Fpnas.172390399",{"id":24,"text":776,"url":24,"identifiers":777},"Ferro, M., Seigneurin-Berny, D., Rolland, N., Chapel, A., Salvi, D., Garin, J., and Joyard, J. (2000). Organic solvent extraction as a versatile procedure to identify hydrophobic chloroplast membrane proteins. Electrophoresis  21  ,  3517–3526.",{"doi":778},"10.1002\u002F1522-2683(20001001)21:16\u003C3517::AID-ELPS3517>3.0.CO;2-H",{"id":24,"text":780,"url":24,"identifiers":781},"Field, H.I., Fenyo, D., and Beavis, R.C. (2002). 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Chem.  72  ,  2482–2489.",{"doi":1140},"10.1021\u002Fac991363o",{"id":1142,"createTime":1143,"updateTime":1144,"relativeEntities":1145,"slug":1146,"properties":1147,"entityType":120,"verifyStatus":121,"verifyTime":1143,"verifyNote":123,"languages":1164,"translateLanguages":24,"viewCount":25,"primaryUrl":1165,"fullTextUrl":24,"authors":1166,"publicationType":177,"publisherRelationship":1260,"citationCount":1310,"citationInfo":1311,"publishDate":1318,"publishYear":1312,"citationAnalyzeStatus":23,"lastCitationAnalyze":1319,"indexDatabases":1320,"openAccess":24,"references":1321,"isForceReanalyzing":494},"c7788d4e-0caf-4387-8151-cfc83ed837aa","2024-09-12T13:53:50.456+00:00","2026-07-13T07:07:35.714+00:00",[],"The-Essential-Nature-of-Sphingolipids-in-Plants-as-Revealed-by-the-Functional-Identification-and-Characterization-of-the-i-Arabidopsis-i-LCB1-Subunit-of-Serine-Palmitoyltransferase",{"mag":1148,"gsPaper":1150,"pmc":1152,"openalex":1154,"abstract":1156,"title":1158,"pm":1160,"doi":1162},{"VOID":1149},"2155156531",{"VOID":1151},"[\"4030402773119161173\"]",{"VOID":1153},"1785403",{"VOID":1155},"W2155156531",{"EN":1157},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Serine palmitoyltransferase (SPT) catalyzes the first step of sphingolipid biosynthesis. In yeast and mammalian cells, SPT is a heterodimer that consists of LCB1 and LCB2 subunits, which together form the active site of this enzyme. We show that the predicted gene for Arabidopsis thaliana LCB1 encodes a genuine subunit of SPT that rescues the sphingolipid long-chain base auxotrophy of Saccharomyces cerevisiae SPT mutants when coexpressed with Arabidopsis LCB2. In addition, homozygous T-DNA insertion mutants for At LCB1 were not recoverable, but viability was restored by complementation with the wild-type At LCB1 gene. Furthermore, partial RNA interference (RNAi) suppression of At LCB1 expression was accompanied by a marked reduction in plant size that resulted primarily from reduced cell expansion. Sphingolipid content on a weight basis was not changed significantly in the RNAi suppression plants, suggesting that plants compensate for the downregulation of sphingolipid synthesis by reduced growth. At LCB1 RNAi suppression plants also displayed altered leaf morphology and increases in relative amounts of saturated sphingolipid long-chain bases. These results demonstrate that plant SPT is a heteromeric enzyme and that sphingolipids are essential components of plant cells and contribute to growth and development.\u003C\u002Fjats:p>",{"EN":1159},"The Essential Nature of Sphingolipids in Plants as Revealed by the Functional Identification and Characterization of the\u003Ci>Arabidopsis\u003C\u002Fi>LCB1 Subunit of Serine Palmitoyltransferase",{"VOID":1161},"17194770",{"VOID":1163},"10.1105\u002Ftpc.105.040774",[125],"https:\u002F\u002Facademic.oup.com\u002Fplcell\u002Farticle\u002F18\u002F12\u002F3576\u002F6115526",[1167,1186,1205,1224,1243],{"id":1168,"sortIndex":25,"researcher":24,"roles":1169,"affiliations":1170,"properties":1179,"displayName":1183,"givenName":24,"familyName":24},"3a88b1b7-a124-47c4-9b5a-d540b9b68b25",[],[1171],{"id":1172,"sortIndex":25,"affiliation":1173,"properties":24},"4c2ac675-95c4-4947-99b5-7484e0d5e6a7",{"id":1172,"createTime":24,"updateTime":24,"relativeEntities":1174,"slug":24,"properties":1175,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1178,"statistic":24},[],{"title":1176},{"VI":1177},"Donald Danforth Plant Science Center, St. Louis, Missouri 63132",[],{"orcid":1180,"title":1182,"openalex":1184},{"VOID":1181},"https:\u002F\u002Forcid.org\u002F0000-0002-9677-1699",{"EN":1183},"Ming Chen",{"VOID":1185},"A5100423292",{"id":1187,"sortIndex":151,"researcher":24,"roles":1188,"affiliations":1189,"properties":1198,"displayName":1202,"givenName":24,"familyName":24},"412b8d06-2c14-45d3-a3da-488fd32c0e48",[],[1190],{"id":1191,"sortIndex":25,"affiliation":1192,"properties":24},"1d17d7a5-fe47-493a-a143-e9ccd9c2a6fb",{"id":1191,"createTime":24,"updateTime":24,"relativeEntities":1193,"slug":24,"properties":1194,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1197,"statistic":24},[],{"title":1195},{"VI":1196},"Department of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814",[],{"orcid":1199,"title":1201,"openalex":1203},{"VOID":1200},"https:\u002F\u002Forcid.org\u002F0000-0001-9927-7939",{"EN":1202},"Gongshe Han",{"VOID":1204},"A5024060695",{"id":1206,"sortIndex":252,"researcher":24,"roles":1207,"affiliations":1208,"properties":1217,"displayName":1219,"givenName":24,"familyName":24},"da6cafb9-6806-4fd6-81cc-9828337848e6",[],[1209],{"id":1210,"sortIndex":25,"affiliation":1211,"properties":24},"dc9d7043-710b-44f3-9fed-a119154c7a87",{"id":1210,"createTime":24,"updateTime":24,"relativeEntities":1212,"slug":24,"properties":1213,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1216,"statistic":24},[],{"title":1214},{"EN":1215},"U.S. Department of Agriculture–Agricultural Research Service, Plant Genetics Research Unit, Donald Danforth Plant Science Center, St. Louis, Missouri 63132",[],{"title":1218,"gsAuthor":1220,"openalex":1222},{"EN":1219},"Charles R. 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We have identified TIP1 by map-based cloning and complementation of the mutant phenotype. TIP1 encodes an ankyrin repeat protein with a DHHC Cys-rich domain that is expressed in roots, leaves, inflorescence stems, and floral tissue. Two homologues of TIP1 in yeast (Saccharomyces cerevisiae) and human (Homo sapiens) have been shown to have S-acyl transferase (also known as palmitoyl transferase) activity. S-acylation is a reversible hydrophobic protein modification that offers swift, flexible control of protein hydrophobicity and affects protein association with membranes, signal transduction, and vesicle trafficking within cells. We show that TIP1 binds the acyl group palmitate, that it can rescue the morphological, temperature sensitivity, and yeast casein kinase2 localization defects of the yeast S-acyl transferase mutant akr1Δ, and that inhibition of acylation in wild-type Arabidopsis roots reproduces the Tip1− mutant phenotype. Our results demonstrate that S-acylation is essential for normal plant cell growth and identify a plant S-acyl transferase, an essential research tool if we are to understand how this important, reversible lipid modification operates in plant cells.\u003C\u002Fjats:p>",{"EN":1599},"The TIP GROWTH DEFECTIVE1  \u003Ci>S\u003C\u002Fi>-Acyl Transferase Regulates Plant Cell Growth in \u003Ci>Arabidopsis\u003C\u002Fi>\n ",{"VOID":1601},"16100337",{"VOID":1603},"10.1105\u002Ftpc.105.031237",[125],"https:\u002F\u002Facademic.oup.com\u002Fplcell\u002Farticle\u002F17\u002F9\u002F2554\u002F6114647",[1607,1628,1645],{"id":1608,"sortIndex":25,"researcher":24,"roles":1609,"affiliations":1610,"properties":1619,"displayName":1623,"givenName":24,"familyName":24},"0b511087-031f-42cd-8a6c-0f8fb7fe7f78",[],[1611],{"id":1612,"sortIndex":25,"affiliation":1613,"properties":24},"c5f7244c-91e7-472f-9a59-fd3f94afce2a",{"id":1612,"createTime":24,"updateTime":24,"relativeEntities":1614,"slug":24,"properties":1615,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1618,"statistic":24},[],{"title":1616},{"VI":1617},"School of Biological Sciences, University of Bristol, Bristol Bs8 1Ug, United Kingdom",[],{"orcid":1620,"title":1622,"gsAuthor":1624,"openalex":1626},{"VOID":1621},"https:\u002F\u002Forcid.org\u002F0000-0003-2950-0634",{"EN":1623},"Piers A. 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While functions of most Aux\u002FIAAs have been defined mainly by gain-of-function mutant alleles in Arabidopsis thaliana, phenotypes associated with loss-of-function mutations have been scarce and subtle. We report here that the downregulation of IAA9, a tomato (Solanum lycopersicum) gene from a distinct subfamily of Aux\u002FIAA genes, results in a pleiotropic phenotype, consistent with its ubiquitous expression pattern. IAA9-inhibited lines have simple leaves instead of wild-type compound leaves, and fruit development is triggered before fertilization, giving rise to parthenocarpy. This indicates that IAA9 is a key mediator of leaf morphogenesis and fruit set. In addition, antisense plants displayed auxin-related growth alterations, including enhanced hypocotyl\u002Fstem elongation, increased leaf vascularization, and reduced apical dominance. Auxin dose–response assays revealed that IAA9 downregulated lines were hypersensitive to auxin, although the only early auxin-responsive gene that was found to be upregulated in the antisense lines was IAA3. The activity of the IAA3 promoter was stimulated in the IAA9 antisense genetic background, indicating that IAA9 acts in planta as a transcriptional repressor of auxin signaling. 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