{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/Canonical_proteome_Ovaries.xlsx"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/checksum.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/39_LA_PC.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/40_LA_PC.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/41_LA_PC.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/38_LA_PC.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/42_LA_PC.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/37_LA_PC.raw"],"Fasta":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD060312/tcons_sequences.fasta"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["palak.chaturvedi@univie.ac.at"],"submitter":["Palak Chaturvedi"],"technology_type":["Mass Spectrometry","Gel-based experiment","Bottom-up proteomics"],"software":[""],"submitter_keywords":["Proteomics on spliceforms","Fruit growth","Tomato","Splicing factors"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD060312"],"tissue":["Plant Ovary"],"sample_protocol":["Sample Processing protocol: For all experiments in this study, Solanum lycopersicum cv. Moneymaker was used as a wild type (WT) or as a background for the generation of mutants. The mutants rs2z35, rs2z36 (here: Cr-rs2z36.1) and the double rs2z35 rs2z36 were described in Rosenkranz et al. (2024). All plants were grown in the greenhouse with a diurnal cycle of 25°C/16 h with 120 µE illumination and 22°C/8 h without illumination."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["Splicing libraries were sequenced at Heinrich Heine University Düsseldorf. These CCS PacBio Isoseq reads were processed with Iso-Seq tools. After sequencing the barcodes, polyA and concatemers were removed from the ccs reads with lima–isoseq (v1.11.0) and isoseq3 refine (v3.3.0). Afterwards the reads were clustered and polished with isoseq3 cluster –split-bam 0 and isoseq3 polish. The processed reads were mapped with pbmm2 align –preset ISOSEQ –sort (v1.3.0) against the reference genome Solanum lycopersicum cv. Heinz version ITAG4.0. For each sample sqanti3 generates a gtf file which was analysed by Eventpointer (v 2.4.0, with R v 3.6.3) to get a qualitative overview of splicing events. Eventpointer identifies alternative splicing events as \"Cassette Exon\", \"Alternative 3' Splice Site\", \"Alternative Last Exon\", \"Retained Intron\", \"Alternative 5' Splice Site\", \"Alternative First Exon\", \"Mutually Exclusive Exons\" and \"Complex Event\". Existing databases were used to generate a splice variant atlas including Isoseq-Tofu, Mikado Transcriptome, NCBI-SRA_2017-2018, and NCBI-SRA_until-2016 (JBrowser from SGN). We merged all with our data using gffcompare (-S –no-merge; v 0.11.6). The tracking file was analyzed to identify shared transcripts within the datasets. Fasta sequences from splice variants were extracted and translated in all three possible forward frames of peptide sequences using the emboss tool transeq -trim -frame F (v. EMBOSS:6.6.0.0). For each translated frame of each transcript the open reading frames (ORF) were taken as input for the proteome discoverer to identify potential peptides. Later the abundant peptides were sorted if they are based on the canonical form or coming from an splice variant only."],"omics_type":["Proteomics"],"labhead":["Palak Chaturvedi"],"instrument_platform":[""],"labhead_affiliation":["University of Vienna"],"submission_type":["PARTIAL"],"species":["Solanum Lycopersicum"],"publication":["42265472 Vraggalas S, Rosenkranz RRE, Keller M, Pérez-Pérez Y, Bachiri S, Zehl KJ, Bold J, Simm S, Ghatak A, Weckwerth W, Afjehi-Sadat L, Chaturvedi P, Testillano PS, Müller-McNicoll M, Zarnack K, Fragkostefanakis S. Splicing regulation by RS2Z36 controls ovary patterning and fruit growth in tomato. Plant Mol Biol. 2026 116(4):65 10.1007/s11103-026-01730-w"],"submitter_mail":["palak.chaturvedi@univie.ac.at"],"submitter_affiliation":["University of Vienna"],"submitter_country":["Austria"],"pubmed_abstract":["Fruit growth is mediated by cell division and expansion. In tomato, the model for fleshy fruit development, both processes are tightly linked to changes in gene expression, including transcriptional regulation and RNA processing. While several transcription factors are implicated in fruit developmental programs, the role of splicing regulators remains largely unexplored. Expression profiling of splicing-related genes revealed expression patterns. The serine/arginine-rich splicing factor RS2Z36 is expressed in ovaries and during early fruit development. Loss-of-function mutations in RS2Z36 result in ovaries with altered patterning and in smaller, ellipsoid fruits. rs2z36 mutants display elongated pericarp cells along the longitudinal axis of pre-anthesis ovaries, indicating that RS2Z36-dependent expansion patterns are established before anthesis. Based on RNA-seq analysis we identified 230 genes with altered splicing profile in ovaries of rs2z36.1 compared to WT and 235 differentially expressed genes. Proteome analysis further revealed several differentially abundant isoforms, including several cell wall proteins and modifiers that might be involved in ovary patterning and fruit growth. In addition, rs2z36-1 pericarps show increased deposition of LM6-recognized arabinan and AGP epitopes. Together, these findings identify RS2Z36 as a regulator of ovary and fruit development and highlight a previously underappreciated role for splicing control in shaping early fruit morphology."],"pubmed_title":["Splicing regulation by RS2Z36 controls ovary patterning and fruit growth in tomato."],"pubmed_authors":["Vraggalas Stavros S, Rosenkranz Remus R E RRE, Keller Mario M, Pérez-Pérez Yolanda Y, Bachiri Samia S, Zehl Kerstin J KJ, Bold Jessica J, Simm Stefan S, Ghatak Arindam A, Weckwerth Wolfram W, Afjehi-Sadat Leila L, Chaturvedi Palak P, Testillano Pilar S PS, Müller-McNicoll Michaela M, Zarnack Kathi K, Fragkostefanakis Sotirios S"],"additional_accession":[]},"is_claimable":false,"name":"Regulation of early-stage tomato fruit growth by the splicing factor RS2Z36","description":"Fruit size and shape are determined by cell division and expansion. In tomato, the model plant for fleshy fruit development, both processes are associated with changes in gene expression including transcription and RNA processing. While several transcription factors have been identified as regulators of genes involved in fruit development, the contribution of splicing regulators remains unknown. Profiling of RNA splicing-related genes revealed stage-preferential expression of several factors, including RS2Z36, a serine/arginine-rich splicing factor highly expressed during the early stages of fruit development. Mutations in RS2Z36 lead to smaller, ellipsoid fruits compared to the wild-type, with histological analysis showing elongated pericarp cells in the ovaries along the longitudinal axis. RNA-seq analysis uncovered numerous alternatively spliced genes involved in different biological processes. Complementary proteome analysis identified proteins with altered abundance and peptides corresponding to novel RNA splice variants, underscoring the role of RS2Z36 in shaping both transcriptome and proteome diversity. Immunofluorescence screening of cell wall proteins further demonstrated an increased abundance of LM6-recognized arabinan epitopes of rhamnogalacturonan-I pectins and arabinogalactan protein (AGP) epitopes in rs2z36-1 pericarp cells compared to the wild type. These findings highlight RS2Z36 as a critical regulator of alternative splicing, impacting fruit development through diverse transcriptome and proteome 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