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TheRLUC gene was altered to contain a modified intron from the castor bean catalase gene while maintaining consensus eukaryotic splicing sites recognized by the plant spliceosome.RLUC andRiLUC reporter genes were fused to the synthetic plant SUPER promoter. Luciferase activity within agrobacteria containing the SUPER-RLUC construct increased during growth in culture. In contrast, agrobacteria harboring the SUPER-RiLUC gene fusion showed no detectable luciferase activity. Agrobacteria containing these gene fusions were cotransformed with a compatible normalization plasmid containing a cauliflower mosaic virus 35S promoter (CaMV) joined to the firefly luciferase coding region (FiLUC) and infused into tobacco leaf tissues through stomatal openings. The kinetics of luciferase production from theRLUC orRiLUC reporters were consistent, with expression of theRiLUC gene being limited to transiently transformed plant cells.RiLUC activity from the reporter gene fusions was measured transiently and within stably transformed tobacco leaf tissues. Analysis of stably transformed tobacco plants harboring either reporter gene fusion showed that the intron altered neither the levels of luciferase activity nor tissue-specific expression patterns driven by the SUPER promoter. These results demonstrate that theRiLUC reporter gene can be used to monitor luciferase expression in transient and stable transformation experiments without interference from contaminating agrobacteria.",{"EN":104},"Construction and testing of an intron-containing luciferase reporter gene fromRenilla reniformis",{"VOID":106},"[\"5231432746248850969\"]",{"VOID":108},"Becker D, Kemper E, Schell J, and Masterson R (1992) New plant binary vectors with selectable markers located proximal to the left T-DNA border. Plant Mol Biol 20(6): 1195–1197.\nBenfey P and Chua N (1990) The cauliflower mosaic virus 35s promoter: combinatorial regulation of transcription in plants. Sci 250(16): 959–966.\nBourdon V, Harvey A, and Lonsdale D (2001) Introns and their positions affect the translational activity of mRNA in plant cells. EMBO Rep 21(51): 394–398.\nHajdukiewicz P, Svab Z, and Maliga P (1994) The small, versatile pPZP family ofAgrobacterium binary vectors for plant transformation. Plant Mol Biol 25: 989–994.\nHorsch R, Fry J, Hoffman N, Neidermeyer J, Rogers S, and Fraley R (1988) Plant Molecular Biology Manual: Leaf Disc Transformation, pp 1–9. Kluwer Academic Publishers, Belgium.\nJefferson R, Kavanagh T, and Bevan M (1987)GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6(13): 3901–3907.\nLeffel S, Mabon S, and Stewart N (1997) Applications of green fluorescent protein in plants. BioTechniques 23: 912–918.\nMankin S, Allen G, and Thompson W (1997) Introduction of a plant intron into the luciferase gene ofPhotinus pyralis. Plant Mol Biol Rep 15(2): 186–196.\nMayerhofer R, Langridge W, Cormier M, and Szalay A (1995) Expression of recombinantRenilla luciferase in transgenic plants results in high levels of light emission. Plant J 7: 1031–1038.\nNi M, Cui D, Einstein J, Narasimhulu S, Vergara Q, and Gelvin S (1995) Strength and tissue specificity of chimeric promoters derived from the octopine and mannopine synthase genes. Plant J 7(4): 661–676.\nOhta S, Mita S, Hattori T, and Nakamura K (1990) Construction and expression in tobacco of a β-glucuronidase (GUS) reporter gene containing an intron within the coding sequence. Plant Cell Physiol 31(6): 805–814.\nOw D, Wood K, DeLuca M, DeWet J, Helsinki D, and Howell S (1986) Transient and stable expression of the firefly luciferase gene in plant cells and transgenic plants. Sci 234 (856–859).\nSambrook J and Russell D (2001) Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, New York.\nShapiro M and Senapathy P (1987) RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression. Nucl Acids Res 15(17): 7155–7174.\nSvab Z, Hajdukiewicz P, and Maliga P (1995) Generation of transgenic tobacco plants by cocultivation of leaf disks withAgrobacterium pPZP binary vectors. In: Methods in Plant Molecular Biology: A Laboratory Course Manual, pp 55–77. Cold Spring Harbor Laboratory Press, New York.\nVancanneyt G, Schmidt R, O'Connor-Sanchez A, Willmitzer L, and Rocha-Sosa M (1990) Construction of an intron-containing marker gene: splicing of the intron in transgenic plants and its use in monitoring early events inAgrobacterium-mediated plant transformation. Mol Gen Genet 220(2): 245–250.\nWalkerpeach C and Velten J (1994)Agrobacterium-mediated gene transfer to plant cells cointegrate and binary vector systems. In: Plant Molecular Biology Manual. pp 1–19 S. Gelvin and R. Schilperoort, Kluwer Academic Publishers, Belgium.",{"VOID":110},"10.1007\u002FBF02772802","PUBLICATION","VERIFIED","2024-05-27T21:01:14.222+00:00","Auto Verify",0,"https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF02772802",[118,136],{"id":119,"sortIndex":115,"researcher":22,"roles":120,"affiliations":122,"properties":131},"6f2a81c8-1d6e-4be6-8466-22829c105f60",[121],"AUTHOR",[123],{"id":124,"sortIndex":115,"affiliation":125,"properties":22},"f9300ec6-9cb2-4c4a-9fce-6e491f1ec1ea",{"id":124,"createTime":22,"updateTime":22,"relativeEntities":126,"slug":22,"properties":127,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":130,"statistic":22},[],{"title":128},{"VI":129},"United States Department of Agriculture-Agricultural Research Services, USDA-ARS, USA",[],{"title":132,"gsAuthor":134},{"VI":133},"Christopher Ian Cazzonelli",{"VOID":135},"[\"M0KCgB4AAAAJ\"]",{"id":137,"sortIndex":138,"researcher":22,"roles":139,"affiliations":140,"properties":147},"d6af8b3b-de1e-4f6b-85d8-0a0f045eeb33",1,[121],[141],{"id":124,"sortIndex":115,"affiliation":142,"properties":22},{"id":124,"createTime":22,"updateTime":22,"relativeEntities":143,"slug":22,"properties":144,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":146,"statistic":22},[],{"title":145},{"VI":129},[],{"title":148},{"VI":149},"Jeff Velten","ARTICLE",{"url":116,"publisher":152,"properties":193},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":153,"slug":10,"properties":154,"entityType":20,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":23,"subjectFields":158,"manageAffiliations":167,"indexDatabases":178,"url":22,"thumbnailPath":22,"statistic":22,"gsStatistic":22,"type":22,"analyzePriority":22},[],{"issn":155,"title":156,"eissn":157},{"VOID":15},{"EN":17},{"VOID":13},[159,163],{"id":26,"createTime":22,"updateTime":22,"relativeEntities":160,"label":161,"description":162,"parentId":22,"standard":22,"scholarHubFieldId":22},[],{"EN":29},{},{"id":32,"createTime":22,"updateTime":22,"relativeEntities":164,"label":165,"description":166,"parentId":22,"standard":22,"scholarHubFieldId":22},[],{"EN":35},{},[168,173],{"id":39,"createTime":22,"updateTime":22,"relativeEntities":169,"slug":22,"properties":170,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":172,"statistic":22},[],{"title":171},{"EN":43},[],{"id":46,"createTime":22,"updateTime":22,"relativeEntities":174,"slug":22,"properties":175,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":177,"statistic":22},[],{"title":176},{"EN":50},[52],[179,186],{"id":73,"indexDatabase":180,"url":84,"indexYears":85,"academicFieldIds":185,"indexDatabaseRanking":89},{"id":75,"createTime":22,"updateTime":22,"relativeEntities":181,"label":182,"description":183,"key":81,"publicationTags":184,"standard":22},[],{"EN":78,"VI":78},{"EN":78,"VI":80},[83],[87,88],{"id":55,"indexDatabase":187,"url":68,"indexYears":22,"academicFieldIds":192,"indexDatabaseRanking":22},{"id":57,"createTime":22,"updateTime":22,"relativeEntities":188,"label":189,"description":190,"key":64,"publicationTags":191,"standard":22},[],{"EN":60,"VI":60},{"EN":62,"VI":63},[66,67],[70,71],{"pages":194,"volume":196},{"VOID":195},"271-280",{"VOID":197},"21",23,{"total":198,"publishYear":200,"statisticByYear":201},2012,{"2004":138,"2005":202,"2006":138,"2008":203,"2009":138,"2011":138,"2012":138,"2014":138,"2015":204,"2016":138,"2019":204,"2023":138,"2024":138,"2025":204,"2026":138},3,4,2,"2012-09-03","DONE_ANALYZE_CITATION","2026-07-25T09:56:00.828+00:00",[89,66],false,{"id":211,"createTime":212,"updateTime":213,"relativeEntities":214,"slug":215,"properties":216,"entityType":111,"verifyStatus":112,"verifyTime":225,"verifyNote":114,"languages":22,"translateLanguages":22,"viewCount":115,"primaryUrl":226,"fullTextUrl":22,"authors":227,"publicationType":150,"publisherRelationship":321,"citationCount":22,"citationInfo":22,"publishDate":368,"publishYear":369,"citationAnalyzeStatus":370,"lastCitationAnalyze":371,"indexDatabases":372,"openAccess":22,"references":22,"isForceReanalyzing":209},"b838edbc-1ea3-4e8c-8172-895e9711178a","2023-12-02T23:18:01.068+00:00","2026-07-25T07:33:43.484+00:00",[],"Direct-ribosomal-RNA-sequencing-Optimization-of-extraction-and-sequencing-methods-for-work-with-higher-plants",{"title":217,"gsPaper":219,"references":221,"doi":223},{"EN":218},"Direct ribosomal RNA sequencing: Optimization of extraction and sequencing methods for work with higher plants",{"VOID":220},"[]",{"VOID":222},"Beaucage, S.L., and M.H. Caruthers (1981). Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis. Tet. Lett. 22:1859–1862.\nChirgwin, J.M., A.E. Przybyla, R.J. MacDonald, and W.J. Rutter. 1979. Isolation of biologically active ribonucleic acid from sources enriched in ribonucleases. Biochemistry 18: 5294–5299.\nDeBorde, D.C., C.W. Naeve, M.L. Herlocher, and H.F. Maassab. 1986. Resolution of a common RNA sequencing ambiguity by terminal deoxynucleotidyl transferase. Anal. Biochem. 157: 275–282.\nDevereux, J., P. Haeberli and O. Smithies. 1984. A comprehensive set of sequence analysis programs for the VAX. Nuc. Acids Res. 12: 387–395.\nEckenrode, V., J. Arnold, and R. Meagher. 1985. Comparison of the nucleotide sequence of soybean 18S rRNA with the sequences of other small subunit rRNAs. J. Mol. Evol. 21: 259–269.\nGlisin, V., R. Crkvenjakov, and C. Byus. 1974. Ribonucleic acid isolated by cesium chloride centrifugation. Biochemistry 13: 2633–2637.\nGutell, R., B. Weiser, C. Woese, and H. Noller. 1985. comparative anatomy of 16-S-like ribosomal RNA. Prog. Nucl. Acid Res. Mol. Biol. 32: 155–216.\nHall, T.C., Y. Ma, B.U. Buchbinder, J.W. Pyne, S.M. Sun, and F.A. Bliss. 1978. Messenger RNA for G1 Protein of French bean seeds: Cell-free translation and product characterization. Proc. Nat. Acad. Sci., USA 75: 3196–3200.\nHamby, R.K., and E.A. Zimmer. 1988. Ribosomal RNA sequences for inferring phylogeny within the grass family (Poaceae). Plant Sys. Evol. in press.\nItakura, K., J.J. Rossi, and R.B. Wallace. 1984. Synthesis and purification of synthetic oligonucleotides. Ann. Rev. Biochem. 53:323–356.\nJupe, E.R., R.L. Chapman, and E.A. Zimmer. 1988. Nuclear ribosomal RNA genes and algal phylogeny—theChlamydomonas example. BioSys. 21:223–230.\nLane, D.J., B. Pace, G.J. Olsen, D.A. Stahl, M.L. Sogin, and N.R. Pace. 1985. Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses. Proc. Natl. Acad. Sci., USA, 82: 6955–6959.\nLane, D.J., K.G. Field, G.J. Olsen, and N.R. Pace. 1988. Reverse transcriptase sequencing of rRNA for phylogenetic analysis. Meth. Enzymol. in press.\nManiatis, T., E. Fritsch, and J. Sambrook. 1982. Molecular Cloning. A laboratory Manual. Cold Spring Harbor Press, Cold Spring Harbor, NY.\nMartin, S., E.A. Zimmer, W. Davidson, A.C. Wilson, and Y.W. Kan. 1981. The untranslated regions of β-globin mRNA evolve at a functional rate in higher primates. Cell 25: 737–741.\nMatteucci, M.D., and M.H. Caruthers. 1981. Synthesis of deoxyoligonucleotides on a polymer support. J. Am. Chem. Soc. 103: 3185–3191.\nMessing, J., J. Carlson, G. Hagen, I. Rubenstein, and A. Oleson. 1984. Cloning and sequencing of the ribosomal RNA genes in maize: The 17S region. DNA 3: 31–40.\nPace, N., G.J. Olsen, and C.R. Woese. 1986. Ribosomal RNA phylogeny and the primary lines of evolutionary descent. Cell 45: 325–326.\nQu, L.H., B. Michot, and J.-P. Bachellerie. 1983. Improved methods for structure probing in large RNAs: A rapid ‘heterologous’ sequencing approach is coupled to the direct mapping of nuclease accessible sites. Application to the 5′ terminal domain of eukaryotic 28S rRNA. Nuc. Acids Res. 11: 5903–5920.\nRubstov, P., M. Musakhanov, V. Zakharyev, A. Krayev, K. Skryabin, and A. Bayev. 1980. The structure of the yeast ribosomal RNA genes. I. The complete nucleotide sequence of the 18S ribosomal RNA gene fromSaccharmyces cerevisiae. Nuc. Acids Res. 8: 5779–5794.\nSaiki, R.K., S. Scharf, F. Faloona, K.B. Mullis, G.T. Horn, H.A. Erlich, and N. Arnheim. 1985. Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science 230:1350–1354.\nSaiki, R.K., D.H. Gelfand, S. Stoffel, S.J. Scharf, R. Higuchi, G.T. Horn, K.B. Mullis, and H.A. Erlich. 1988. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239: 487–491.\nSalim, M., and B. Maden. 1981. Nucleotide sequence ofXenopus laevis 18S ribosomal RNA inferred from gene sequence. Nature 291: 205–208.\nTakaiwa, F., and M. Sugiura. 1982. The complete nucleotide sequence of a 23S rRNA gene from tobacco chloroplasts. Eur. J. Biochem. 124:13–19. Takaiwa, F., K. Oono, and M. Sugiura. 1984. The complete nucleotide sequence of a rice 17S rRNA gene. Nuc. Acids Res. 12: 5441–5448.\nTakaiwa, F., K. Oona, Y. Iida, and M. Sugiura. 1985. The complete nucleotide sequence of a rice 25S rRNA gene. Gene 37: 255–289.\nTohdoh, N., and M. Suguira. 1982. The complete nucleotide sequence of a 16S ribosomal RNA molecule from tobacco chloroplasts. Gene 17: 213–218.\nTolan, D., A.B. Amsden, S. Putney, M. Urdea, and E.E. Penhoet. 1984. The complete nucleotide sequence for rabbit muscle aldolase A messenger RNA. J. Biol. Chem. 259: 1127–1131.\nTorczynski, R., A. Bollon, and M. Fuke. 1983. The complete nucleotide sequence of the rat 18S ribosomal RNA gene and comparison with the respective yeast and frog genes. Nuc. Acids Res. 11: 4879–4890.\nYouvan, D., and J. Hearst. 1981. A sequence fromDrosophila melanogaster 18S rRNA bearing the conserved hypermodified nucleoside amΨ. Analysis by reverse transcription and high-performance liquid chromatography. Nucleic. Acids Res. 9: 1723–1741.\nZimmer, E.A., and L.E. Sims. 1985. Ribosomal gene yardsticks of plant molecular evolution: Direct DNA sequencing analyses. ICPMB Abstracts 1: 88.",{"VOID":224},"10.1007\u002FBF02669591","2024-09-04T21:58:10.230+00:00","http:\u002F\u002Flink.springer.com\u002F10.1007\u002FBF02669591",[228,252,272,292],{"id":229,"sortIndex":115,"researcher":22,"roles":230,"affiliations":231,"properties":249},"7f6bf28d-77a1-4fcf-9371-f4fe15660b32",[121],[232,240],{"id":233,"sortIndex":115,"affiliation":234,"properties":22},"39a1b02d-8c63-4a84-b5ba-1a987dce1a01",{"id":233,"createTime":22,"updateTime":22,"relativeEntities":235,"slug":22,"properties":236,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":239,"statistic":22},[],{"title":237},{"VI":238},"Department of Biochemistry, Louisiana State University, Baton Rouge, USA",[],{"id":241,"sortIndex":138,"affiliation":242,"properties":248},"ed909815-affa-4404-bc76-aeacd696060c",{"id":241,"createTime":22,"updateTime":22,"relativeEntities":243,"slug":22,"properties":244,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":247,"statistic":22},[],{"title":245},{"VI":246},"Louisiana Agricultural Experiment Station, LSU Agricultural Center, Baton Rouge, USA",[],{},{"title":250},{"VI":251},"R. 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Plant Mol Biol 56:309–323\nChu CC, Wang CC, Sun CS, Hsu C, Yin KC, Chu CY, Bi FY (1975) Establishment of an efficient medium for anther culture of rice through comparative experiments on the nitrogen sources. Sci Sinica 18:659–668\nDaí S, Zheng P, Marmey P, Zhang S, Tian WZ, Chen SY, Beachy RN, Fau C (2001) Comparative analysis of transgenic rice plants obtained by Agrobacterium-mediated transformation and particle bombardment. Mol Breeding 7:25–33\nDaram P, Brunner S, Person BL, Amrhein N, Bucher M (1998) Functional analysis and cell-specific expression of a phosphate transporter from tomato. Planta 206:225–233\nFagard M, Vaucheret H (2000) (Trans)gene silencing in plants: how many mechanisms? Annu Rev Plant Physiol Plant Mol Biol 51:167–194\nFrame B, Zhang H, Cocciolone S, Sidorenko L, Dietrich C, Pegg S, Zhen S, Schnable P, Wang K (2000) Production of transgenic maize from bombarded type II callus: effect of gold particle size and callus morphology on transformation efficiency. In Vitro Cell Dev Biol Plant 36:21–29\nFuente JM, Ramírez-Rodríguez V, Cabrera-Ponce JL, Herrera-Estrella L (1997) Aluminum tolerance in transgenic plants by alteration of citrate synthesis. Science 276:1566–1568\nHobbs SL, Warkentin TD, DeLong CM (1993) Transgene copy number can be positively and negatively associated with transgene expression. Plant Mol Biol 21:17–26\nHobbs SL, Kpodar P, DeLong CM (1990) The effect of T-DNA copy number, position and methylation on reporter gene expression in tobacco transformants. Plant Mol Biol 15:851–864\nIBGE—INSTITUTO BRASILEIRO DE GEOGRAFIA E ESTATÍSTICA (2009) Levantamento sistemático da produção agrícola. http:\u002F\u002Fwww.ibge.com.br. Accessed 21 Dec 2009\nJefferson RA, Kavanaugh TA, Bevan MW (1987) Gus fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6:3001–3907\nKarthikeyan AS, Varadarajan DK, Mukatira UT, D’uszo MP, Damz B, Raghothama KG (2002) Regulated expression of Arabidopsis phosphate transporters I. Plant Physiol 130:221–233\nLeggewie G, Willmitzer L, Riesmeier JW (1997) Two cDNAs from potato are able to complement a phosphate uptake-deficient yeast mutant: identification of phosphate transporters from higher plants. Plant Cell 9:381–392\nLiu CM, Muchhal US, Uthappa M, Kononowicz AK, Raghothama KG (1998) Tomato phosphate transporter genes are differentially regulated in plant tissues by phosphorus. Plant Physiol 116:91–99\nMagnavaca R (1982) Genetic variability and the inheritance of aluminum tolerance in maize (Zea mays L.). 135 p. Ph.D. Thesis, University of Nebraska, Nebraska\nMartinez E (2002) Multi-protein complexes in eukaryotic gene transcription. Plant Mol Biol 50:925–947\nMuchhal US, Pardo JM, Raghotama KG (1996) Phosphate transporters from the higher plant Arabidopsis thaliana. Proc Natl Acad Sci USA 93:10519–10523\nMurashige T, Skoog FA (1962) Revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol Plant 15:473–497\nRaghothama KG (1999) Phosphate acquisition. Annu Rev Plant Physiol Plant Mol Biol 50:665–693\nRombauts S, Florquin K, Lescot M, Marchal K, Rouzé P, Van De Peer Y (2003) Computational approaches to identify promoter and cis-regulatory elements in plant genomes. Plant Physiol 132:1162–1176\nSaghai-Maroof MA, Soliman KM, Jorgensen RA, Allard RW (1984) Ribosomal DNA spacer-length polymorphisms in barley: mendelian inheritance, chromosomal location, and population dynamics. Proc Natl Acad Sci USA 81:8014–8018\nSambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor\nSchubert D, Lechtenberg B, Forsbach A, Gils M, Bahadur S, Schimidt R (2004) Silencing in Arabidopsis T-DNA transformants: the predominant role of gene-specific RNA sensing mechanism versus position effects. Plant Cell 16:2561–2572\nShou H, Frame BR, Whitham AS, Wang K (2004) Assessment of transgenic maize events produced by particle bombardment or Agrobacterium-mediated transformation. 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The functions of CSDPs have been studied in Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa), wheat (Triticum aestivum), and Chinese cabbage (Brassica rapa). To gain insight into the function of CSDPs in tomato (Solanum lycopersicum), we performed a genome-wide analysis of CSDPs through in silico characterization and expression profiling in different organs and in response to different abiotic stress and phytohormone treatments. We identified five non-redundant SlCSDP genes. The evolutionary analysis and phylogenetic classification indicated that tomato CSDPs are more closely related to potato than those of others. The five SlCSDP genes are distributed on four of the 12 tomato chromosomes and no segmental or tandem duplication events are detected among them. Expression analysis showed broad expression patterns with strong expression in fruit development and ripening. Expression of individual SlCSDP genes was significantly altered by stress and phytohormone treatments. SlCSDP2, SlCSDP3, and SlCSDP4 were highly induced by all four abiotic stresses and by phytohormone treatment in tomato. These findings provide a foundation for future research towards functional biological roles of CSDP gene in particular to develop tomato cultivars with large size, early ripening, and abiotic stress tolerance.",{"EN":733},"Expression Profiling of the CSDP Transcription Factor Gene Family Points to Roles in Organ Development and Abiotic Stress Response in Tomato (Solanum lycopersicum L.)",{"VOID":220},{"VOID":736},"Aoki K, Yano K, Suzuki A, Kawamura S, Sakurai N, Suda K, Ooga K (2010) Large-scale analysis of full length cDNAs from the tomato (Solanum lycopersicum) cultivar Micro-Tom, a reference system for the Solanaceae genomics. BMC Genomics 11:210\nBeauchemin M, Roy S, Pelletier S, Averback A, Lanthier F, Morse D (2016) Characterization of two dinoflagellate cold shock domain proteins. mSphere 1:e00034–e00015\nChaikam V, Karlson D (2008) Functional characterization of two cold shock domain proteins from Oryza sativa. Plant Cell Environ 31:995–1006\nChoi MJ, Park YR, Park SJ, Kang H (2015) Stress-responsive expression patterns and functional characterization of cold shock domain proteins in cabbage (Brassica rapa) under abiotic stress conditions. Plant Physiol Biochem 96:132–140\nChorey M, Carmel L (2012) The function of Introns. Front Genet 3:55\nClark AJ, Archibald AL, McClenaghan M, Simons JP, Wallace R, Whitelaw CB (1993) Enhancing the efficiency of transgene expression. Philos Trans R Soc Lond B Biol Sci 339:225–232\nFusaro AF, Bocca SN, Ramos RLB, Barroco RM, Magioli C, Jorge VC, Coutinho TC, Rangel-Lima CM, De Rycke R, Inzé D, Engler G, Sachetto-Martins G (2007) AtGRP2, a cold-induced nucleo-cytoplasmic RNA-binding protein, has a role in flower and seed development. Planta 225:1339e1351\nGraumann PL, Marahiel MA (1998) A super family of proteins that contain the cold-shock domain. Trends Biochem Sci 23:286–290\nHorn XG, Hofweber R, Kremer W, Kalbitzer HR (2007) Structure and function of bacterial cold shock proteins. Mol Cell Life Sci 64:1457–1470\nJuneau K, Miranda M, Hillenmeyer ME, Nislow C, Davis RW (2006) Introns regulate RNA and protein abundance in yeast. Genetics 174:511–518\nKarlson D, Imai R (2003) Conservation of the cold shock domain protein family in plants. Plant Physiol 131:12–15\nKarlson D, Nakaminami K, Toyomasu T, Imai R (2002) A cold-regulated nucleic acid-binding protein of winter wheat shares a domain with bacterial cold shock proteins. J Biol Chem 277:35248–35256\nKhatun K, Robin AHK, Park JI, Kim CK, Lim KB, Kim MB, Lee DJ, Nou IS, Chung MY (2016) Genome-wide identification, characterization and expression profiling of ADF family genes in Solanum lycopersicum L. Genes 7:79\nKim MH, Sasaki K, Imai R (2009) Cold shock domain protein 3 regulates freezing tolerance in Arabidopsis thaliana. J Biol Chem 284:23454–23460\nKim MH, Sato S, Sasaki K, Saburi W, Matsui H, Imai R (2013) Cold shock domain protein 3 is involved in salt and drought stress tolerance in Arabidopsis. FEBS Open Bio 3:438–442\nKong X, Lv W, Jiang S, Zhang D, Cai G, Pan J, Li D (2013) Genome-wide identification and expression analysis of calcium-dependent protein kinase in maize. BMC Genomics 14:433\nLorkovic ZJ (2009) Role of plant RNA-binding proteins in development, stress response and genome organization. Trends Plant Sci 14:229–236\nLorkovic ZJ, Barta A (2002) Genome analysis: RNA recognition motif (RRM) and K homology (KH) domain RNA-binding proteins from the flowering plant Arabidopsis thaliana. Nucleic Acids Res 30:623–635\nNakaminami K, Karlson DT, Imai R (2006) Functional conservation of cold shock domains in bacteria and higher plants. Proc Natl Acad Sci 103:10122–10127\nNakaminami K, Hill K, Perry SE, Sentoku N, Long JA, Karlson D (2009) Arabidopsis cold shock domain proteins: relationships to floral and silique development. J Exp Bot 60:1047e1062\nPark SJ, Kwak KJ, Oh TR, Kim YO, Kang H (2009) Cold shock domain proteins affect seed germination and growth of Arabidopsis thaliana under abiotic stress conditions. Plant Cell Physiol 50:869e878\nRadkova M, Vítámvás P, Sasaki K, Imai R (2014) Development and cold-regulated accumulation of cold shock domain proteins in wheat. Plant Physiol Biochem 77:44–48\nSachetto-Martins G, Franco LO, de Oliveira DE (2000) Plant glycine-rich proteins: a family or just proteins with a common motif? Biochem Biophys Acta 1492:1–14\nSasaki K, Imai R (2011) Pleiotropic roles of cold shock domain proteins in plants. Front Plant Sci 2:116\nSasaki K, Kim MH, Imai R (2007) Arabidopsis cold shock domain protein 2 is a RNA chaperone that is regulated by cold and developmental signals. Biochem Biophys Res Commun 364:633e638\nSchmittgen TD, Livak KJ (2008) Analyzing real-time PCR data by the comparative CT method. Nat Protoc 3:1101–1108\nSkabkin MA, Skabkina OV, Ovchinnikov LP (2004) Multifunctional cold shock domain containing proteins in regulation of gene expression. Usp Biol Khim 44:3–52\nSorek R, Ast G (2003) Intronic sequences flanking alternatively spliced exons are conserved between human and mouse. Genome Res 13:1631–1637\nTamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol 30:2725–2729\nValencia P, Dias AP, Reed R (2008) Splicing promotes rapid and efficient mRNA export in mammalian cells. Proc Natl Acad Sci 105:3386–3391\nWang L, Guo K, Li Y, Tu Y, Hu H, Wang B, Peng L (2010) Expression profiling and integrative analysis of the CESA\u002FCSL superfamily in rice. BMC Plant Biol 10:282\nWu J, Peng Z, Liu S, He Y, Cheng L, Kong F, Lu G (2012) Genome-wide analysis of Aux\u002FIAA gene family in Solanaceae species using tomato as a model. Mol Gen Genomics 287:295–311",{"VOID":738},"10.1007\u002Fs11105-018-1075-1","2024-06-26T19:20:48.757+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11105-018-1075-1",[742,757,781,794,809,822],{"id":743,"sortIndex":115,"researcher":22,"roles":744,"affiliations":745,"properties":754},"1ca1cf6c-2ad5-48f5-aae3-004654168dcb",[121],[746],{"id":747,"sortIndex":115,"affiliation":748,"properties":22},"04a7b800-149b-4089-ae95-fe241f66993a",{"id":747,"createTime":22,"updateTime":22,"relativeEntities":749,"slug":22,"properties":750,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":753,"statistic":22},[],{"title":751},{"VI":752},"Department of Agricultural Industry Economy and Education, Sunchon National University, Suncheon, Korea",[],{"title":755},{"VI":756},"Khadiza 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embryogenesis abundant (LEA) proteins are identified as a large and highly diverse group of polypeptides accumulating in response to cellular dehydration in many organisms. However, there are only very limited reports of this protein family in maize until this study. In the present paper, we identified 32 LEA genes in maize. A total of 83 LEA proteins including 51 members in Arabidopsis and 32 putative members in maize were classified into nine groups. Gene organization and motif compositions of the LEA members are highly conserved in each of the groups, indicative of their functional conservation. The predicted ZmLEA genes were non-random distributed across chromosomes, and transposition event and segmental duplication contributed to the expansion of the LEA gene family in maize. Some abiotic stress-responsive cis-elements were also found in the promoters of ZmLEA genes. Microarray expression analyses revealed different accumulation patterns of ZmLEA family members. Moreover, some members of ZmLEAs were regulated under IAA and some abiotic stresses. This study will provide comprehensive information for maize LEA gene family and may pave the way for deciphering their functions in further studies.",{"EN":905},"Late Embryogenesis Abundant (LEA) Gene Family in Maize: Identification, Evolution, and Expression Profiles",{"VOID":220},{"VOID":908},"Bailey TL, Williams N, Misleh C, Li WW (2006) MEME: discovering and analyzing DNA and protein sequence motifs. Nucleic Acids Res 34(Web Server issue):W369–W373\nBattaglia M, Covarrubias AA (2013) Late embryogenesis abundant (LEA) proteins in legumes. Front Plant Sci 4:190\nBlanc G, Wolfe KH (2004) Widespread paleopolyploidy in model plant species inferred from age distributions of duplicate genes. Plant Cell 16(7):1667–1678\nCandat A, Paszkiewicz G, Neveu M, Gautier R, Logan DC, Avelange-Macherel MH, Macherel D (2014) The ubiquitous distribution of late embryogenesis abundant proteins across cell compartments in Arabidopsis offers tailored protection against abiotic stress. 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Biotechnol Biotechnol Equip 29(5):861–868",{"doi":1319},"10.1080\u002F13102818.2015.1056753",{"id":22,"text":1321,"url":22,"identifiers":1322},"Tomato Genome Consortium x (2012) The tomato genome sequence provides insights into fleshy fruit evolution. Nature 485(7400):635",{"doi":1323},"10.1038\u002Fnature11119",{"id":22,"text":1325,"url":22,"identifiers":1326},"Van Eck J, Keen P, Tjahjadi M (2019) Agrobacterium tumefaciens-mediated transformation of tomato Transgenic Plants. Springer p 225–234",{"doi":1327},"10.1007\u002F978-1-4939-8778-8_16",{"id":22,"text":1329,"url":22,"identifiers":1330},"Van Eck J, Kirk DD, Walmsley AM (2006) Tomato (Lycopersicum esculentum) Agrobacterium Protocols. Springer p 459–474",{},{"id":22,"text":1332,"url":22,"identifiers":1333},"van Roekel JSC, Damm B, Melchers LS, Hoekema A (1993) Factors influencing transformation frequency of tomato (Lycopersicon esculentum). Plant Cell Rep 12(11):644–647. https:\u002F\u002Fdoi.org\u002F10.1007\u002FBF00232816",{"doi":1334},"10.1007\u002FBF00232816",{"id":22,"text":1336,"url":22,"identifiers":1337},"Yang L, Shen H, Pan A, Chen J, Huang C, Zhang D (2005) Screening and construct-specific detection methods of transgenic Huafan No 1 tomato by conventional and real-time PCR. J Sci Food Agric 85(13):2159–2166",{"doi":1338},"10.1002\u002Fjsfa.2193",{"id":22,"text":1340,"url":22,"identifiers":1341},"Yasmeen A (2009) An improved protocol for the regeneration and transformation of tomato (cv Rio Grande). Acta Physiol Plant 31(6):1271. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11738-009-0364-6",{"doi":1342},"10.1007\u002Fs11738-009-0364-6",{"id":1344,"createTime":1345,"updateTime":1346,"relativeEntities":1347,"slug":1348,"properties":1349,"entityType":111,"verifyStatus":112,"verifyTime":1360,"verifyNote":114,"languages":22,"translateLanguages":22,"viewCount":115,"primaryUrl":1361,"fullTextUrl":22,"authors":1362,"publicationType":150,"publisherRelationship":1491,"citationCount":115,"citationInfo":1538,"publishDate":1541,"publishYear":1539,"citationAnalyzeStatus":21,"lastCitationAnalyze":1346,"indexDatabases":1542,"openAccess":22,"references":22,"isForceReanalyzing":209},"ce2adcf0-e92f-499b-810b-25ae13e27a6b","2024-01-14T06:57:47.610+00:00","2026-07-12T18:44:26.864+00:00",[],"Identification-and-Functional-Analysis-of-Two-Cotton-Orthologs-of-MAX2-Which-Control-Shoot-Lateral-Branching",{"abstract":1350,"title":1352,"gsPaper":1354,"references":1356,"doi":1358},{"EN":1351},"Cotton (Gossypium spp.), as the most important fiber and oilseed crop in the world, is extremely important for the industry. However, due to its indeterminate growth habit and complex branching system, massive labor costs are needed for shoot apex removal and branch pruning during cotton production. Therefore, it is very important to explore branch-controlling genes and genetically modify the branch architecture of cotton. Strigolactones (SLs) are a novel class of plant hormone that inhibit the outgrowth of lateral branches. To elucidate the role of SLs in branch development of cotton, we cloned and characterized GhMAX2a and GhMAX2b from tetraploid upland cotton (Gossypium hirsutum), the orthologs of Arabidopsis MAX2, rice D3, and petunia RMS4. GhMAX2a\u002F2b was ubiquitously expressed in all tested tissues of cotton, with relatively higher expression levels in leaves and lateral buds. Subcellular localization assay showed that the GhMAX2-GFP fusion protein localized to the nucleus. Both GhMAX2a and GhMAX2b can fully rescue the dwarfed and highly branched phenotypes of the Arabidopsis max2-1 mutant, indicating that GhMAX2s have conserved functions with that of AtMAX2. The cotton GhMAX2b interacted with Arabidopsis Skp1-like 1 (ASK1) proteins in vitro which was further confirmed in the Arabidopsis protoplasts using the co-immunoprecipitation assay, indicating that GhMAX2b probably functions through forming an SCF E3 complex with Skp and other proteins in the Arabidopsis. These results suggest that the cotton GhMAX2s encode functional MAX2 that can inhibit the shoot lateral branching. Further functional analysis of GhMAX2s in determining cotton branch architecture and yield is underway.",{"EN":1353},"Identification and Functional Analysis of Two Cotton Orthologs of MAX2 Which Control Shoot Lateral Branching",{"VOID":1355},"[\"9351860868717886669\"]",{"VOID":1357},"Alder A, Jamil M, Marzorati M et al (2012) The path from beta-carotene to carlactone, a strigolactone-like plant hormone. Science 335:1348–1351\nAleman L, Kitamura J, Abdel-mageed H et al (2008) Functional analysis of cotton orthologs of GA signal transduction factors GID1 and SLR1. Plant Mol Biol 68:1–16\nArgiriou A, Michailidis G, Tsaftaris AS (2008) Characterization and expression analysis of TERMINAL FLOWER1 homologs from cultivated alloteraploid cotton (Gossypium hirsutum) and its diploid progenitors. J Plant Physiol 165:1636–1646\nArite T, Iwata H, Ohshima K et al (2007) DWARF10, an RMS1\u002FMAX4\u002FDAD1 ortholog, controls lateral bud outgrowth in rice. Plant J 51:1019–1029\nArite T, Umehara M, Ishikawa S, Hanada A, Maekawa M, Yamaguchi S, Kyozuka J (2009) d14, a strigolactone-insensitive mutant of rice, shows an accelerated outgrowth of tillers. Plant Cell Physiol 50:1416–1424\nBennett T, Sieberer T, Willett B, Booker J, Luschnig C, Leyser O (2006) The Arabidopsis MAX pathway controls shoot branching by regulating auxin transport. Curr Biol 16:553–563\nBeveridge CA (2006) Axillary bud outgrowth: sending a message. Curr Opin Plant Biol 9:35–40\nBooker J, Auldridge M, Wills S, McCarty D, Klee H, Leyser O (2004) MAX3\u002FCCD7 is a carotenoid cleavage dioxygenase required for the synthesis of a novel plant signaling molecule. Curr Biol 14:1232–1238\nBooker J, Sieberer T, Wright W et al (2005) MAX1 encodes a cytochrome P450 family member that acts downstream of MAX3\u002F4 to produce a carotenoid-derived branch-inhibiting hormone. Dev Cell 8:443–449\nBrameier M, Krings A, Maccallum RM (2007) NucPred - Predicting nuclear localization of proteins. Bioinformatics 23:1159–60\nClough SJ, Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16:735–743\nCook CE, Whichard LP, Turner B, Wall ME, Egley GH (1966) Germination of Witchweed (Striga lutea Lour.): isolation and properties of a potent stimulant. Science 154:1189–1190\nCook CE, Whichard LP, Monroe WE, Egley GH, Coggon P, Luhan PA, Mcphail AT (1972) Germination stimulants. II. Structure of strigol, a potent seed germination stimulant for witchweed (Striga lutea). J Am Chem Soc 94:6198–6199\nDong HZ, Li WJ, Li ZH, Tang W, Zhang DM (2003) Review on utilization of vegetative branches of cotton plants. Cotton Science 15(5):313–317\nDrummond RS, Martinez-Sanchez NM, Janssen BJ et al (2009) Petunia hybrida carotenoid cleavage dioxygenase7 is involved in the production of negative and positive branching signals in petunia. Plant Physiol 151:1867–1877\nFerguson BJ, Beveridge CA (2009) Roles for auxin, cytokinin, and strigolactone in regulating shoot branching. Plant Physiol 149:1929–1944\nFoo E, Bullier E, Goussot M, Foucher F, Rameau C, Beveridge CA (2005) The branching gene RAMOSUS1 mediates interactions among two novel signals and auxin in pea. Plant Cell 17:464–474\nGomez-Roldan V et al (2008) Strigolactone inhibition of shoot branching. Nature 455:189–194\nHamiaux C, Drummond RS, Janssen BJ, Ledger SE, Cooney JM, Newcomb RD, Snowden KC (2012) DAD2 is an alpha\u002Fbeta hydrolase likely to be involved in the perception of the plant branching hormone, strigolactone. Curr Biol 22:2032–2036\nIqbal MJ, Ouk R, Elzik KM, Pepper AE (2001) A genetic bottleneck in the ‘evolution under domestication’ of upland cotton Gossypium hirsutum L. examined using DNA fingerprinting. Theor Appl Genet 103(4):547–554\nIshikawa S, Maekawa M, Arite T, Onishi K, Takamure I, Kyozuka J (2005) Suppression of tiller bud activity in tillering dwarf mutants of rice. Plant Cell Physiol 46:79–86\nJiang L, Liu X, Xiong G et al (2013) DWARF 53 acts as a repressor of strigolactone signalling in rice. Nature 504:401–405\nJohnson X, Brcich T, Dun EA, Goussot M, Haurogne K, Beveridge CA, Rameau C (2006) Branching genes are conserved across species. Genes controlling a novel signal in pea are coregulated by other long-distance signals. Plant Physiol 142:1014–1026\nLechner E, Achard P, Vansiri A, Potuschak T, Genschik P (2006) F-box proteins everywhere. Curr Opin Plant Biol 9:631–638\nLi F, Fan G, Wang K et al (2014) Genome sequence of the cultivated cotton Gossypium arboreum. Nat Genet 46:567–572\nLi F, Fan G, Lu C et al (2015) Genome sequence of cultivated upland cotton (Gossypium hirsutum TM-1) provides insights into genome evolution. Nat Biotechnol 33:524–530\nLin H, Wang R, Qian Q et al (2009) DWARF27, an iron-containing protein required for the biosynthesis of strigolactones, regulates rice tiller bud outgrowth. Plant Cell 21:1512–1525\nLópez-Ráez JA, Charnikhova T, Gomez-Roldan V et al (2008) Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation. New Phytol 178:863–874\nMatusova R, Rani K, Verstappen FW, Franssen MC, Beale MH, Bouwmeester HJ (2005) The strigolactone germination stimulants of the plant-parasitic Striga and Orobanche spp. are derived from the carotenoid pathway. 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Plant J 48:687–698",{"VOID":1359},"10.1007\u002Fs11105-017-1040-4","2024-05-17T04:01:30.748+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11105-017-1040-4",[1363,1387,1400,1413,1426,1439,1452,1465,1478],{"id":1364,"sortIndex":115,"researcher":22,"roles":1365,"affiliations":1366,"properties":1384},"7abe9d43-1660-4851-9b64-6ecbb8718a8c",[121],[1367,1375],{"id":1368,"sortIndex":115,"affiliation":1369,"properties":22},"0d6523d8-5af0-4e81-9913-4636d858e79e",{"id":1368,"createTime":22,"updateTime":22,"relativeEntities":1370,"slug":22,"properties":1371,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":1374,"statistic":22},[],{"title":1372},{"VI":1373},"National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China",[],{"id":1376,"sortIndex":138,"affiliation":1377,"properties":1383},"89867889-4afe-4beb-8d34-420cbe084019",{"id":1376,"createTime":22,"updateTime":22,"relativeEntities":1378,"slug":22,"properties":1379,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":1382,"statistic":22},[],{"title":1380},{"VI":1381},"College of Life Sciences, Liaocheng University, Liaocheng, China",[],{},{"title":1385},{"VI":1386},"Linlin 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pseudostem weevil (Odoiporus longicollis) is an important insect pest of banana which causes significant reduction in yields in many countries across the world. This study evaluated the transcriptome profile of O. longicollis infested resistant banana cultivar Musa paradisiaca cv. ‘Kachkal’ for the first time and identified differentially expressed genes (DEGs) modulated during the host-pest interaction. RNA sequencing of the transcriptome of O. longicollis infested banana cultivar with respect to control revealed 2429 and 118 significantly upregulated and downregulated genes, respectively. The genes upregulated during the O. longicollis-M. paradisiaca interaction were classified into 83 Gene Ontology (GO) classes of biological processes (BP), 47 classes of molecular function (MF), and 10 classes of cellular component (CC), while the downregulated genes were classified into 10 classes of BP, 6 classes of MF, and 2 classes of CC. Further, the KEGG pathway enrichment analysis revealed 36 pathways associated with upregulated genes and 6 pathways with downregulated genes. Several defense-related genes significantly and highly upregulated in ‘Kachkal’ in response to pseudostem weevil infestation, were found to have functions related to linoleic acid metabolism (lipoxygenase), response to biotic stress (PR4, PR1 like, mannose\u002Fglucose-specific lectins), amino and nucleotide sugar metabolism (phospholipase, chitinase 6, chitinase 10, endochitinase), peptidase inhibitor activity (Bowman-Birk type proteinase inhibitor-like), catalytic activity (terpene synthase, allene oxide synthase 2-like), protein kinase pathway (MAPK), biosynthesis of secondary metabolite (jasmonate), metabolic pathways (alpha amylase), sequence-specific DNA binding (WRKY), and molecular transcription (EtRP). Ten defense response–related genes, significantly upregulated in the banana cultivar upon O. longicollis infestation, were selected as important candidates for qRT-PCR validation. The expression patterns of the selected genes successfully validated the RNA sequencing results and at the same time established the potentiality of the genes in conferring defense or tolerance to herbivory by the insect pest. The study has generated substantial data in relation to defense-associated reprogramming of the M. paradisiaca cv. Kachkal transcriptome in response to attack by O. longicollis.",{"EN":1553},"Molecular Dissection of the Odoiporus longicollis Infested Musa paradisiaca Transcriptome Reveals Key Genes Involved in Defense",{"VOID":1555},"[\"13496876221637457854\"]",{"VOID":1557},"10.1007\u002Fs11105-022-01368-0","2024-04-30T05:20:49.239+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11105-022-01368-0",[1561,1585,1600],{"id":1562,"sortIndex":115,"researcher":22,"roles":1563,"affiliations":1564,"properties":1582},"ed768c1a-9a79-42e3-aa3c-9f44a303a7e1",[121],[1565,1573],{"id":1566,"sortIndex":115,"affiliation":1567,"properties":22},"1ac566f1-fbd0-409f-b9b8-23f3bb28d10e",{"id":1566,"createTime":22,"updateTime":22,"relativeEntities":1568,"slug":22,"properties":1569,"entityType":22,"verifyStatus":22,"verifyTime":22,"verifyNote":22,"languages":22,"translateLanguages":22,"viewCount":22,"url":22,"parentIds":1572,"statistic":22},[],{"title":1570},{"VI":1571},"Department of 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