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Base J represses genes at the end of polycistronic gene clusters in Leishmania major by promoting RNAP II termination

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-187727
  • The genomes of kinetoplastids are organized into polycistronic gene clusters that are flanked by the modified DNA base J. Previous work has established a role of base J in promoting RNA polymerase II termination in Leishmania spp. where the loss of J leads to termination defects and transcription into adjacent gene clusters. It remains unclear whether these termination defects affect gene expression and whether read through transcription is detrimental to cell growth, thus explaining the essential nature of J. We now demonstrate that reductionThe genomes of kinetoplastids are organized into polycistronic gene clusters that are flanked by the modified DNA base J. Previous work has established a role of base J in promoting RNA polymerase II termination in Leishmania spp. where the loss of J leads to termination defects and transcription into adjacent gene clusters. It remains unclear whether these termination defects affect gene expression and whether read through transcription is detrimental to cell growth, thus explaining the essential nature of J. We now demonstrate that reduction of base J at specific sites within polycistronic gene clusters in L. major leads to read through transcription and increased expression of downstream genes in the cluster. Interestingly, subsequent transcription into the opposing polycistronic gene cluster does not lead to downregulation of sense mRNAs. These findings indicate a conserved role for J regulating transcription termination and expression of genes within polycistronic gene clusters in trypanosomatids. In contrast to the expectations often attributed to opposing transcription, the essential nature of J in Leishmania spp. is related to its role in gene repression rather than preventing transcriptional interference resulting from read through and dual strand transcription.zeige mehrzeige weniger

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Autor(en): David L. Reynolds, Brigitte T. Hofmeister, Laura Cliffe, T. Nicolai Siegel, Britta A. Andersson, Stephen M. Beverley, Robert J. Schmitz, Robert Sabatini
URN:urn:nbn:de:bvb:20-opus-187727
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Molecular Microbiology
Erscheinungsjahr:2016
Band / Jahrgang:101
Heft / Ausgabe:4
Seitenangabe:559-574
Originalveröffentlichung / Quelle:Molecular Microbiology (2016) 101:4, 559-574. https://doi.org/10.1111/mmi.13408
DOI:https://doi.org/10.1111/mmi.13408
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):Cruzi; DNA; Expression; Genome; Glucosyltransferase; Hydroxymethyluracil; Messenger RNA; Parasite; Transcription initiation; Trypanosoma-brucei
Datum der Freischaltung:17.06.2020
Lizenz (Deutsch):License LogoCC BY-NC-ND: Creative-Commons-Lizenz: Namensnennung, Nicht kommerziell, Keine Bearbeitungen 4.0 International