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Campo DCValorIdioma
dc.contributor.authorBarros, Mario H.-
dc.contributor.authorMyers, Alan M.-
dc.contributor.authorVan Driesche, Sarah-
dc.contributor.authorTzagoloff, Alexander-
dc.date.accessioned2014-05-27T11:21:49Z-
dc.date.accessioned2016-10-25T18:21:56Z-
dc.date.available2014-05-27T11:21:49Z-
dc.date.available2016-10-25T18:21:56Z-
dc.date.issued2006-02-10-
dc.identifierhttp://dx.doi.org/10.1074/jbc.M510778200-
dc.identifier.citationJournal of Biological Chemistry, v. 281, n. 6, p. 3743-3751, 2006.-
dc.identifier.issn0021-9258-
dc.identifier.issn1083-351X-
dc.identifier.urihttp://hdl.handle.net/11449/68779-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68779-
dc.description.abstractIn most strains of Saccharomyces cerevisiae the mitochondrial gene COX1, for subunit 1 of cytochrome oxidase, contains multiple exons and introns. Processing of COX1 primary transcript requires accessory proteins factors, some of which are encoded by nuclear genes and others by reading frames residing in some of the introns of the COX1 and COB genes. Here we show that the low molecular weight protein product of open reading frame YLR204W, for which we propose the name COX24, is also involved in processing of COX1 RNA intermediates. The growth defect of cox24 mutants is partially rescued in strains harboring mitochondrial DNA lacking introns. Northern blot analyses of mitochondrial transcripts indicate cox24 null mutants to be blocked in processing of introns aI2 and aI3. The dependence of intron aI3 excision on Cox24p is also supported by the growth properties of the cox24 mutant harboring mitochondrial DNA with different intron compositions. The intermediate phenotype of the cox24 mutant in the background of intronless mitochondrial DNA, however, suggests that in addition to its role in splicing of the COX1 pre-mRNA, Cox24p still has another function. Based on the analysis of a cox14-cox24 double mutant, we propose that the other function of Cox24p is related to translation of the COX1 mRNA. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.en
dc.format.extent3743-3751-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBiochemistry-
dc.subjectEnzymes-
dc.subjectGenes-
dc.subjectMolecular biology-
dc.subjectMolecular weight-
dc.subjectMutagenesis-
dc.subjectRNA-
dc.subjectYeast-
dc.subjectExons-
dc.subjectIntrons-
dc.subjectMitochondrial protein-
dc.subjectMutants-
dc.subjectProteins-
dc.subjectcyclooxygenase 1-
dc.subjectcyclooxygenase 24 enzyme-
dc.subjectmitochondrial DNA-
dc.subjectmitochondrial protein-
dc.subjectunclassified drug-
dc.subjectCOX24 protein, S cerevisiae-
dc.subjectcytochrome c oxidase-
dc.subjectepitope-
dc.subjectfungal DNA-
dc.subjecthemagglutinin-
dc.subjectmessenger RNA-
dc.subjectSaccharomyces cerevisiae protein-
dc.subjectcontrolled study-
dc.subjectenzyme localization-
dc.subjectintron-
dc.subjectmolecular cloning-
dc.subjectnonhuman-
dc.subjectNorthern blotting-
dc.subjectopen reading frame-
dc.subjectphenotype-
dc.subjectpriority journal-
dc.subjectprotein expression-
dc.subjectprotein function-
dc.subjectprotein processing-
dc.subjectRNA splicing-
dc.subjectSaccharomyces-
dc.subjectsequence alignment-
dc.subjectyeast-
dc.subjectamino acid sequence-
dc.subjectbiosynthesis-
dc.subjectchemistry-
dc.subjectenzymology-
dc.subjectfungal gene-
dc.subjectgenetics-
dc.subjectmetabolism-
dc.subjectmitochondrion-
dc.subjectmolecular genetics-
dc.subjectmutation-
dc.subjectSaccharomyces cerevisiae-
dc.subjectsequence homology-
dc.subjectspecies difference-
dc.subjectAmino Acid Sequence-
dc.subjectBlotting, Northern-
dc.subjectCloning, Molecular-
dc.subjectDNA, Fungal-
dc.subjectDNA, Mitochondrial-
dc.subjectElectron Transport Complex IV-
dc.subjectEpitopes-
dc.subjectGenes, Fungal-
dc.subjectHemagglutinins-
dc.subjectMitochondria-
dc.subjectMitochondrial Proteins-
dc.subjectMolecular Sequence Data-
dc.subjectMutation-
dc.subjectOpen Reading Frames-
dc.subjectPhenotype-
dc.subjectRNA, Messenger-
dc.subjectSaccharomyces cerevisiae Proteins-
dc.subjectSequence Homology, Amino Acid-
dc.subjectSpecies Specificity-
dc.titleCOX24 codes for a mitochondrial protein required for processing of the COX1 transcripten
dc.typeoutro-
dc.contributor.institutionColumbia University-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionIowa State University-
dc.description.affiliationDepartment of Biological Sciences Columbia University, New York, NY 10027-
dc.description.affiliationDept. of Genetics IBB-UNESP, Botucatu/SP 18607-741-
dc.description.affiliationDept. of Biochemistry, Biophysics and Molecular Biology Iowa State University, Ames, IA 50011-
dc.description.affiliationUnespDept. of Genetics IBB-UNESP, Botucatu/SP 18607-741-
dc.identifier.doi10.1074/jbc.M510778200-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Biological Chemistry-
dc.identifier.scopus2-s2.0-33645649913-
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