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

Please always quote using this 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.show moreshow less

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Metadaten
Author: 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
Document Type:Journal article
Faculties:Medizinische Fakultät
Language:English
Parent Title (English):Molecular Microbiology
Year of Completion:2016
Volume:101
Issue:4
Pagenumber:559-574
Source:Molecular Microbiology (2016) 101:4, 559-574. https://doi.org/10.1111/mmi.13408
DOI:https://doi.org/10.1111/mmi.13408
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:Cruzi; DNA; Expression; Genome; Glucosyltransferase; Hydroxymethyluracil; Messenger RNA; Parasite; Transcription initiation; Trypanosoma-brucei
Release Date:2020/06/17
Licence (German):License LogoCC BY-NC-ND: Creative-Commons-Lizenz: Namensnennung, Nicht kommerziell, Keine Bearbeitungen 4.0 International