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Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake.

Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Research Abstract Details 

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  • Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Abstract Text:

    carleton l kingsfordCarleton L Kingsford,kunmi ayanbuleKunmi Ayanbule,steven l salzbergSteven L Salzberg,

    BACKGROUND: In many prokaryotes, transcription of DNA to RNA is terminated by a thymine-rich stretch of DNA following a hairpin loop. Detecting such Rho-independent transcription terminators can shed light on the organization of bacterial genomes and can improve genome annotation. Previous computational methods to predict Rho-independent terminators have been slow or limited in the organisms they consider. RESULTS: We describe TransTermHP, a new computational method to rapidly and accurately detect Rho-independent transcription terminators. We predict the locations of terminators in 343 prokaryotic genomes, representing the largest collection of predictions available. In Bacillus subtilis, we can detect 93% of known terminators with a false positive rate of just 6%, comparable to the best-known methods. Outside the Firmicutes division, we find that Rho-independent termination plays a large role in the Neisseria and Vibrio genera, the Pasteurellaceae (including the Haemophilus genus) and several other species. In Neisseria and Pasteurellaceae, terminator hairpins are frequently formed by closely spaced, complementary instances of exogenous DNA uptake signal sequences. We quantify the propensity for terminators to include these sequences. In the process, we provide the first discussion of potential uptake signals in Haemophilus ducreyi and Mannheimia succiniciproducens, and we discuss the preference for a particular configuration of uptake signal sequences within terminators. CONCLUSION: Our new fast and accurate method for detecting transcription terminators has allowed us to identify and analyze terminators in many new genomes and to identify DNA uptake signal sequences in several species where they have not been previously reported. Our software and predictions are freely available.

    Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Publishing Authors By Initials

    cl kingsfordCL Kingsford,k ayanbuleK Ayanbule,sl salzbergSL Salzberg,

    For similar genetic processes: gene expression: transcription, genetic research abstracts see: genetic processes: gene expression: transcription, genetic research

    PUBMED ID PMID:

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    Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Genome biology

    VOLUME: 8

    Page Numbers: R22

    Journal Abbreviation:

    ISSN: 1465-6914

    DAY: 3

    MONTH: 12

    YEAR: 2007

    Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100960660

    Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Keywords Mesh Terms:

    KEYWORDS: Transcription, Genetic

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake. Information

    Substance Name: DNA

    Registry Number: 9007-49-2

    Grant and Affiliation Information for Rapid, accurate, computational discovery of Rho-independent transcription terminators illuminates their relationship to DNA uptake.

    AFFILIATION: Center for Bioinformatics and Computational Biology, University of Maryland, College Park, MD 20742, USA. carlk@umiacs.umd.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NLM

    GRANT: R01-LM06845

    ACRONYM: LM

    MEDLINETA: Genome Biol

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