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Rusché LN, Piller KJ, Sollner-Webb B: Guide RNA-mRNA chimeras, which are potential RNA editing intermediates, are formed by endonuclease and RNA ligase in a trypanosome mitochondrial extract. Mol Cell Biol 1995, 15:2933-2941. An elegant paper in which much evidence is presented in favor of the cleavage/ligation model of chimera formation. The best argument is that an isolated 3′ cleavage fragment of the pre-mRNA is a far better substrate for chimera formation than the intact molecule.
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Seiwert SD, Stuart K: Transfer of genetic information from guide RNA to precursor mRNA in vitro. Science 1994, 266:114-117. The first clear sign that continued efforts to develop kinetoplastid in vitro editing systems may in the end succeed: two Us from an editing site in ATPase 6 pre-mRNA are removed in a T. brucei mitochondrial extract dependent on the presence of a specific gRNA and ATP. Base-pairing interactions between gRNA and pre-mRNA determine the number of Us deleted.
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Byrne E, Bringaud F, Simpson L: RNA-protein interactions in the ribonucleoprotein T-complexes in a mitochondrial extract from Leishmania tarentolae. Mol Biochem Parasitol 1995, 72:65-76.
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Read LK, Göringer HU, Stuart K: Assembly of mitochondrial ribonucleoprotein complexes involves specific guide RNA (gRNA)-binding proteins and gRNA domains but does not require pre-edited mRNA. Mol Cell Biol 1994, 14:2629-2639.
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Yu W, Schuster W: Evidence for a site-specific cytidine deamination reaction involved in C to U RNA editing in plant mitochondria. J Biol Chem 1995, 270:18227-18233. A demonstration in vitro and in organello that plant mitochondrial editing also involves post-transcriptional site-specific C deamination.
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Chauduri S, Carrer H, Maliga P: Site-specific factor involved in the editing of the psbL mRNA in tobacco plastids. EMBO J 1995, 14:2951-2957. Chimeric gene constructs containing the amino-terminal part of the tobacco psbL gene are introduced by ballistic gene targeting into the tobacco plastid genome. Surprisingly, the editing of endogenous psbL RNA is inhibited whereas that of rpoB and ndhB RNA is unaffected. This suggests the involvement of site-specific factors in plastid RNA editing.
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Sutton CA, Zoubenko OV, Hanson MR, Maliga P: A plant mitochondrial sequence transcribed in tobacco chloroplasts is not edited. Mol Cell Biol 1995, 15:1377-1381. A Petunia cytochrome c oxidase subunit 2 transcript containing seven editing sites is not edited in tobacco plastids. This indicates the existence of organelle-specific components.
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Arraya A, Domec C, Begu D, Litvak S: An in vitro system for the editing of ATP synthase subunit 9 mRNA using wheat mitochondrial extracts. Proc Natl Acad Sci USA 1992, 89:1040-1044.
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Bock R, Maliga P: In vivo testing of a tobacco plastid DNA segment for guide RNA function in psbL editing. Mol Gen Genet 1995, 247:439-443.
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Gott JM, Visomirski LM, Hunter JL: Substitutional and insertional editing of the cytochrome c oxidase subunit mRNA of Physarum polycephalum. J Biol Chem 1993, 268:25483-25486.
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Riley GR, Myler PJ, Stuart K: Quantitation of RNA editing substrates, products and potential intermediates: implications for developmental regulation. Nucleic Acids Res 1995, 23:708-712.
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Grohmann L, Thieck O, Herz U, Schröder W, Brennicke A: Translation of nad9 mRNAs in mitochondria from Solanum tuberosum is restricted to completely edited transcripts. Nucleic Acids Res 1994, 22:3304-3311. One of the few papers that deals with the protein products of edited mRNAs. Despite the presence of many partially edited (potential) mRNAs, only fully edited mRNA is used for translation. This suggests that the editing and translation processes are physically separated.
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Nucleic Acids Res
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Grohmann, L.1
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Landweber LF, Gilbert W: RNA editing as a source of genetic variation. Nature 1993, 363:179-182.
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Hiesel R, Combattes B, Brennicke A: Evidence for RNA editing in mitochondria of all major groups of land plants except the Bryophyta. Proc Natl Acad Sci USA 1994, 91:629-633.
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Landweber LF, Gilbert W: Phylogenetic analysis of RNA editing: a primitive genetic phenomenon. Proc Natl Acad Sci USA 1994, 91:918-921.
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Simpson L, Maslov DA: Ancient origin of RNA editing in kinetoplastid protozoa. Curr Opin Genet Dev 1994, 4:887-894. A clear account of current thoughts on the phylogeny of kinetoplastid RNA editing. Although ancient in the kinetoplastid lineage, U insertion/deletion editing has not been found anywhere else. The paper describes a model for the evolution of kinetoplastid editing based on retrotransposition into the genome of edited and partially edited cDNAs. The model does not explain, however, how present-day mRNAs with only small internal editing regions (such as trypanosomatid cox2) have arisen.
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Curr Opin Genet Dev
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Novel pattern of editing reigons in mitochondrial transcripts of the cryptobiid Trypanoplasma borreli
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Lukes J, Arts GJ, Van den Burg J, De Haan A, Opperdoes F, Sloof P, Benne R: Novel pattern of editing reigons in mitochondrial transcripts of the cryptobiid Trypanoplasma borreli. EMBO J 1994, 13:5086-5098.
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Lukes, J.1
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On the evolution of RNA editing
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Covello P, Gray MW: On the evolution of RNA editing. Trends Genet 1993, 9:265-268.
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Hepatitis D virus RNA editing: Specific modification of adenosine in the antigenomic RNA
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Casey JL, Gerin JL: Hepatitis D virus RNA editing: specific modification of adenosine in the antigenomic RNA. J Virol 1995, 69:7593-7600. It was long unclear whether the editing of HDV RNA is the result of a U to C transition in the genomic strand or an A modification (to I or G) in the antigenomic strand. In this paper the confusion is resolved through the analysis of non-replicating genomic and antigenomic HDV RNAs, the results of which favor mechanisms invoking editing by A deamination of the antigenomic strand. Analogous to GluR-B mRNA editing, HDV RNA editing requires basepairing, making dsRAD a likely candidate enzyme in this case too.
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(1995)
J Virol
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Casey, J.L.1
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