NusG Is a Sequence-specific RNA Polymerase Pause Factor That Binds to the Non-template DNA within the Paused Transcription Bubble.

Yakhnin, Alexander V; Murakami, Katsuhiko S; Babitzke, Paul

Yakhnin, Alexander V; Murakami, Katsuhiko S; Babitzke, Paul.

Afiliación

Yakhnin AV; From the Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, Pennsylvania 16802.
Murakami KS; From the Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, Pennsylvania 16802.
Babitzke P; From the Department of Biochemistry and Molecular Biology, Center for RNA Molecular Biology, Pennsylvania State University, University Park, Pennsylvania 16802 pxb28@psu.edu.

J Biol Chem ; 291(10): 5299-308, 2016 Mar 04.

Article en En | MEDLINE | ID: mdl-26742846

RESUMEN

NusG, referred to as Spt5 in archaeal and eukaryotic organisms, is the only transcription factor conserved in all three domains of life. This general transcription elongation factor binds to RNA polymerase (RNAP) soon after transcription initiation and dissociation of the RNA polymerase σ factor. Escherichia coli NusG increases transcription processivity by suppressing RNAP pausing, whereas Bacillus subtilis NusG dramatically stimulates pausing at two sites in the untranslated leader of the trpEDCFBA operon. These two regulatory pause sites participate in transcription attenuation and translational control mechanisms, respectively. Here we report that B. subtilis NusG makes sequence-specific contacts with a T-rich sequence in the non-template DNA (ntDNA) strand within the paused transcription bubble. NusG protects T residues of the recognition sequence from permanganate oxidation, and these T residues increase the affinity of NusG to the elongation complex. Binding of NusG to RNAP does not require interaction with RNA. These results indicate that bound NusG prevents forward movement of RNA polymerase by simultaneously contacting RNAP and the ntDNA strand. Mutational studies indicate that amino acid residues of two short regions within the NusG N-terminal domain are primarily responsible for recognition of the trp operon pause signals. Structural modeling indicates that these two regions are adjacent to each another in the protein. We propose that recognition of specific sequences in the ntDNA and stimulation of RNAP pausing is a conserved function of NusG-like transcription factors.

Asunto(s)

Proteínas Bacterianas/metabolismo; ADN Bacteriano/metabolismo; Regulación Bacteriana de la Expresión Génica; Factores de Elongación Transcripcional/metabolismo; Secuencia de Aminoácidos; Bacillus subtilis/genética; Proteínas Bacterianas/química; Proteínas Bacterianas/genética; Secuencia de Bases; Datos de Secuencia Molecular; Unión Proteica; Elongación de la Transcripción Genética; Factores de Elongación Transcripcional/química; Factores de Elongación Transcripcional/genética

Palabras clave

NusG; RNA polymerase; RNA polymerase pausing; bacterial transcription; gene regulation; protein-DNA interaction; transcription elongation factor

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Bacterianas / ADN Bacteriano / Regulación Bacteriana de la Expresión Génica / Factores de Elongación Transcripcional Tipo de estudio: Prognostic_studies Idioma: En Revista: J Biol Chem Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos

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