{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_WT2_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_OE3_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_OE1_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_WT3_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_MSS2_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_MSS3_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_MSS1_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_OE2_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_WT2_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_WT1_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_OE3_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_MSS2_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_OE1_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_WT3_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_MSS1_TR02.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_MSS3_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_OE2_TR01.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/b023p018_WT1_TR01.raw"],"Fasta":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/Uniprot_Cerevisiae_20160815.fasta"],"Other":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/04/PXD008785/txt.zip"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":204,"searchCount":0},"additional":{"labhead_mail":["tobias.warnecke@imperial.ac.uk"],"submitter":["Holger Kramer"],"technology_type":["Mass Spectrometry","Shotgun proteomics"],"software":["Not available"],"submitter_keywords":["mss116","mitochondria","Yeast mitochondrial fraction","Yeast mitochondrial fraction; mitochondria; mss116"],"full_dataset_link":["http://www.ebi.ac.uk/pride/archive/projects/PXD008785"],"sample_protocol":["Protein samples were processed by trypsin digestion using the FASP protocol on 30kDa molecular weight cut-off concentrators. LC-MS/MS analysis was performed on a U3000 RSLC nanoflow chromatography system using a 50cm column coupled via an Easyspray source to a LTQ Orbitrap Velos tandem mass spectrometer which was operated in CID fragmentation mode."],"repository":["Pride"],"quantification_method":["Not available"],"modification":["iodoacetamide derivatized residue"],"data_protocol":["The data was analysed using MaxQuant (v1.6.0.1) using the label-free quantification (LFQ) algorithm. The preselected standard search parameters were used unless stated otherwise. The database search was performed against the Uniprot Saccharomyces cerevisiae database (v20160815, 6729 entries). LFQ settings were as follows, Minimum ratio count: 2; Fast LFQ: disabled; Match between runs: enabled; Match time window: 1.0 min; Alignment time window: 20min."],"omics_type":["Proteomics"],"labhead":["Tobias Warnecke"],"instrument_platform":["LTQ Orbitrap Velos"],"submission_type":["PARTIAL"],"labhead_affiliation":["MRC London Institute of Medical Sciences Hammersmith Hospital Campus Du Cane Road London, W12 0NN United Kingdom"],"species":["Saccharomyces Cerevisiae (baker's Yeast)"],"publication":["29570052 Rudan M, Bou Dib P, Musa M, Kanunnikau M, Sobočanec S, Rueda D, Warnecke T, Kriško A. Normal mitochondrial function in Saccharomyces cerevisiae has become dependent on inefficient splicing. Elife. 2018 7 10.7554/elife.35330"],"submitter_mail":["h.kramer@lms.mrc.ac.uk"],"curator_keywords":["Biological"],"submitter_affiliation":["MRC London Institute of Medical Sciences"],"submitter_country":["United Kingdom"],"pubmed_abstract":["Self-splicing introns are mobile elements that have invaded a number of highly conserved genes in prokaryotic and organellar genomes. Here, we show that deletion of these selfish elements from the Saccharomyces cerevisiae mitochondrial genome is stressful to the host. A strain without mitochondrial introns displays hallmarks of the retrograde response, with altered mitochondrial morphology, gene expression and metabolism impacting growth and lifespan. Deletion of the complete suite of mitochondrial introns is phenocopied by overexpression of the splicing factor Mss116. We show that, in both cases, abnormally efficient transcript maturation results in excess levels of mature cob and cox1 host mRNA. Thus, inefficient splicing has become an integral part of normal mitochondrial gene expression. We propose that the persistence of S. cerevisiae self-splicing introns has been facilitated by an evolutionary lock-in event, where the host genome adapted to primordial invasion in a way that incidentally rendered subsequent intron loss deleterious."],"pubmed_title":["Normal mitochondrial function in Saccharomyces cerevisiae has become dependent on inefficient splicing."],"pubmed_authors":["Rudan Marina M, Bou Dib Peter P, Musa Marina M, Kanunnikau Matea M, Sobočanec Sandra S, Rueda David D, Warnecke Tobias T, Kriško Anita A"],"sample_synonyms":["liquid chromatography tandem mass spectroscopy, l(4)17, cenpA., l(4)13, TAFII30, Gli, l(1)VE614, Molecular Weights, determination, Cid[Mel], Ci[D], protein, combined T cell and B cell immunodeficiency, protein-containing complex, body system, combined T and B cell immunodeficiency, CENP-A, LC-MS-MS, CENP-C, CenpA, Cut, l(4)102ABc, protein polypeptide chains, method, AU041226, polypeptide chain, l(1)7Ba, l(1)7Bb, method used in an experiment, 30kDa, LC-MSMS, system, protein aggregate, Siah, CenH3[Cid], CG13329, CenH3[CID], anatomical systems, BcDNA:RE21270, LCMSMS, Molecular, beta-Trypsin, DmelCG13329, Weights, proteins, kf, CG11387, Acdc, X-linked combined immunodeficiency, Taf2h, CI, DmelCG11387, column, Cenp-A, CT, CG2125, Chromatographies, CiD, combined immunodeficiency, LC-MS2, Ce, Ci, protein complex, Ct, LC-MS/MS, cenH3, C79664, collisionally activated dissociation, CID, ciD, Cid, adipo, LC/MS/MS, CAD, native protein, natural protein, ci[D], Ci155, Protein, Weight, chemical analysis, ci-D, BcDNA:GH10590, connected anatomical system, DmelCG2125, ci155, CenH3, Ci/Gli, Ci/GLI, CenH3/CID, CENP-A/Cid, CENP-A/CID, CENPA, Acrp30, Tripcellim, study protocol, beta Trypsin, GBP28, apM1, plan specification, incised, organ system, congenital combined immunodeficiency, Trypure, liquid chromatography-tandem mass spectroscopy, liquid chromatography tandem mass spectrometry, assay, CenpA/CID, Ci-155, APN, CID/CENP-A"],"pubmed_title_synonyms":["Normalities, Saccharomyces oviformis, average, Individual Health, Yeast, Mitochondrial, nuclear mRNA cis splicing, Normality, Saccharomyces cerevisiae 'var. diastaticus', Brewer's, via spliceosome., baker's yeast, Baker, function, Normalcy, Saccharomyces uvarum var. melibiosus, Normalcies, mitochondrial, splicing, Saccharomyces italicus, S. cerevisiae, Baker's Yeasts, via U2-type spliceosome, Health, S cerevisiae, Candida robusta, ATP synthase D chain, Saccharomyces capensis, Saccharomyces diastaticus, Baker's, Mycoderma cerevisiae, Individual, Baker's Yeast, brewer's yeast, Brewer's Yeast, Baker Yeast"],"data_synonyms":["data, DYRK1, Saccharomyces cerevisiae 'var. diastaticus', Effects, Longterm., STK10, Brewer's, Longterm Effect, Dmel_CG7826, baker's yeast, FASTK, Saccharomyces italicus, Long Term, CG7826, Baker's Yeasts, period, count, Dm1, Saccharomyces diastaticus, Algorithm, Long Term Effects, CG7835, CG42273, Min, Dyrk1, Effect, Dmel_CG7835, Data Base, DmelCG42273, Saccharomyces oviformis, Mnb, MNB, AU020952, Yeast, proportion, Longterm, CC1, proportionality, min, rate, mAPC, Baker, Long-Term, AW124434, Saccharomyces uvarum var. melibiosus, free, Fast, Longterm Effects, S. cerevisiae, ME-IV, AI047805, S cerevisiae, Candida robusta, Saccharomyces capensis, ATP:Fas-activated serine/threonine protein phosphotransferase activity, quotient, Baker's, Mycoderma cerevisiae, Long-Term Effect, Baker's Yeast, brewer's yeast, Brewer's Yeast, time, Long-Term Effects, FAST, Baker Yeast, ratio"],"description_synonyms":["ATPsyn-&bgr, RNA, Ribonucleic, nuclear mRNA cis splicing, ATPsyn-b, Saccharomyces cerevisiae 'var. diastaticus', ribose nucleic acid, ribonucleic acids, Brewer's, via spliceosome., baker's yeast, RNS, IB, splicing, Saccharomyces italicus, Concept, ATP-syn-B, Baker's Yeasts, Role Concept, ML-1, Roles, Saccharomyces diastaticus, yeast nucleic acid, ATP-synbeta, Ribonukleinsaeure, Role, Gene Products, Concepts, pentosenucleic acids, Ribonucleic acids, Non Polyadenylated, RNA Gene Products, CG11154, Saccharomyces oviformis, study, ribonucleic acid, Acid, Yeast, DmelCG11154, Non Polyadenylated RNA, beta-ATPase, Non-Polyadenylated, Baker, Ribonucleic Acid, Saccharomyces uvarum var. melibiosus, S. cerevisiae, Non-Polyadenylated RNA, via U2-type spliceosome, S cerevisiae, ATPsyn b, Candida robusta, ATPasebeta, Saccharomyces capensis, ATPase beta, ATPIB, Role Concepts, Baker's, Mycoderma cerevisiae, Baker's Yeast, brewer's yeast, Brewer's Yeast, ATPB, Baker Yeast, ATP"],"pubmed_abstract_synonyms":["biochemical pathways, host organism, Metabolic Process, lifespan, nuclear mRNA cis splicing, Materials, cox1, Processes, postnatal development, number, Metabolic Concepts, Brewer's, PCOX1, PHS1, via spliceosome, Gene, baker's yeast, histology, growth and development, Metabolic Processes, mitochondrial signalling pathway, splicing, mitochondrial, Normalcies, Saccharomyces italicus, element, corncob, maize cob, PHS 1, Metabolism, Concepts, Metabolism Concept, Phenomenon, Metabolism Phenomena, Normalities, average, MSL3_40, Genetic, Gene Expressions, mitochondrial genome, Genomes, catabolism, entire lifespan, entire life cycle, Metabolic Concept, messenger RNA, MSL3.40, Baker, metabolic process resulting in cell growth, number of, COX3, Saccharomyces uvarum var. melibiosus, COX1, MTCO1, Expressions, ecotype, COI, S. cerevisiae, via U2-type spliceosome, mitochondrial signaling pathway, template RNA, S cerevisiae, Candida robusta, Saccharomyces capensis, has or lacks parts of type, corn cob, Baker's, biotransformation, Intron, Mycoderma cerevisiae, Expression, elements, brewer's yeast, cob, Catabolism, INSDC_feature:intron., atom, CoxI, retrograde response, ATR, PTGHS, Individual Health, degradation, Process, Saccharomyces cerevisiae 'var. diastaticus', Intervening Sequences, metabolism resulting in cell growth, extra or missing physical or functional parts, Pghs1, Normalcy, Cistrons, INSDC_feature:misc_RNA, results, strain, Concept, Metabolic Phenomena, mereological quality, Sequences, Baker's Yeasts, development, Metabolism Concepts, Intervening Sequence, PES-1, PGHS1, ATP synthase D chain, Saccharomyces diastaticus, Sequence, Phenomena, INSDC_feature:mRNA, Genetic Materials, atomo, atomus, secretion, cultivar, Individual, atome, metabolism, Genetic Material, Metabolic Phenomenon, Saccharomyces oviformis, mitochondria-nucleus signal transduction, Yeast, Mitochondrial, multicellular organism metabolic process, mtDNA, Element, PGG/HS, protein_coding_transcript, biodegradation, Metabolic, growth pattern, mRNA, Normality, non-developmental growth, life, atoms, COBRA, postnatal growth, cblB, Intervening, CFAP23, single-organism metabolic process, Health, mitochondrial DNA, PGHS-1, Material, DEL, cardinality, Cistron, rachis, Cox-1, Cox-3, Baker's Yeast, growth, Brewer's Yeast, Baker Yeast, Anabolism"],"name_synonyms":["Saccharomyces oviformis, liquid chromatography tandem mass spectroscopy, LC-MS2, Yeast, LCMSMS, Saccharomyces cerevisiae 'var. diastaticus', LC-MS/MS, Brewer's, baker's yeast, Baker, Saccharomyces uvarum var. melibiosus, Saccharomyces italicus, S. cerevisiae, Baker's Yeasts, S cerevisiae, LC/MS/MS, Candida robusta, Saccharomyces capensis, Saccharomyces diastaticus, liquid chromatography-tandem mass spectroscopy, LC-MSMS, Baker's, liquid chromatography tandem mass spectrometry, LC-MS-MS., Mycoderma cerevisiae, Baker's Yeast, brewer's yeast, Brewer's Yeast, Baker Yeast"],"view_count":["204"],"additional_accession":[]},"is_claimable":true,"name":"Saccharomyces cerevisiae mitochondrial fractions by LC-MS/MS","description":"Investigation into the role of the Saccharomyces cerevisiae ATP-dependent RNA helicase MSS116 in mitochondrial 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