Literature DB >> 27125778

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

David L Reynolds1, Brigitte T Hofmeister2, Laura Cliffe1, T Nicolai Siegel3, Britta A Anderson4, Stephen M Beverley4, Robert J Schmitz5, Robert Sabatini1.   

Abstract

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 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.
© 2016 The Authors. Molecular Microbiology Published by John Wiley & Sons Ltd.

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Year:  2016        PMID: 27125778      PMCID: PMC5038137          DOI: 10.1111/mmi.13408

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  48 in total

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Authors:  Christine E Clayton
Journal:  EMBO J       Date:  2002-04-15       Impact factor: 11.598

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Authors:  David A Campbell; Sean Thomas; Nancy R Sturm
Journal:  Microbes Infect       Date:  2003-11       Impact factor: 2.700

3.  Inactivation of transcription by UV irradiation of T. brucei provides evidence for a multicistronic transcription unit including a VSG gene.

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Journal:  Eukaryot Cell       Date:  2011-09-16

5.  Glucosylated hydroxymethyluracil, DNA base J, prevents transcriptional readthrough in Leishmania.

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Journal:  Cell       Date:  2012-08-31       Impact factor: 41.582

6.  Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymine glucosylation of DNA.

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7.  JBP1 and JBP2 proteins are Fe2+/2-oxoglutarate-dependent dioxygenases regulating hydroxylation of thymidine residues in trypanosome DNA.

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8.  Transcriptomic profiling of gene expression and RNA processing during Leishmania major differentiation.

Authors:  Laura A L Dillon; Kwame Okrah; V Keith Hughitt; Rahul Suresh; Yuan Li; Maria Cecilia Fernandes; A Trey Belew; Hector Corrada Bravo; David M Mosser; Najib M El-Sayed
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  8 in total

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Review 3.  Leishmania-Host Interactions-An Epigenetic Paradigm.

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5.  Genetic Interaction Between Site-Specific Epigenetic Marks and Roles of H4v in Transcription Termination in Trypanosoma brucei.

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Review 6.  Impact of Genetic Diversity and Genome Plasticity of Leishmania spp. in Treatment and the Search for Novel Chemotherapeutic Targets.

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Review 7.  Histone Modifications and Other Facets of Epigenetic Regulation in Trypanosomatids: Leaving Their Mark.

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