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TOR Facilitates the Targeting of the 19S Proteasome Subcomplex To Enhance Transcription Complex Assembly at the Promoters of the Ribosomal Protein Genes.

Identifieur interne : 000482 ( Main/Exploration ); précédent : 000481; suivant : 000483

TOR Facilitates the Targeting of the 19S Proteasome Subcomplex To Enhance Transcription Complex Assembly at the Promoters of the Ribosomal Protein Genes.

Auteurs : Bhawana Uprety [États-Unis] ; Amala Kaja [États-Unis] ; Sukesh R. Bhaumik [États-Unis]

Source :

RBID : pubmed:29712756

Descripteurs français

English descriptors

Abstract

TOR (target of rapamycin) has been previously implicated in transcriptional stimulation of the ribosomal protein (RP) genes via enhanced recruitment of NuA4 (nucleosome acetyltransferase of H4) to the promoters. However, it is not clearly understood how TOR enhances NuA4 recruitment to the promoters of the RP genes. Here we show that TOR facilitates the recruitment of the 19S proteasome subcomplex to the activator to enhance the targeting of NuA4 to the promoters of the RP genes. NuA4, in turn, promotes the recruitment of TFIID (transcription factor IID, composed of TATA box-binding protein [TBP] and a set of TBP-associated factors [TAFs]) and RNA polymerase II to the promoters of the RP genes to enhance transcriptional initiation. Therefore, our results demonstrate that TOR facilitates the recruitment of the 19S proteasome subcomplex to the promoters of the RP genes to promote the targeting of NuA4 for enhanced preinitiation complex (PIC) formation and consequently transcriptional initiation, hence illuminating TOR regulation of RP gene activation. Further, our results reveal that TOR differentially regulates PIC formation (and hence transcription) at the non-RP genes, thus demonstrating a complex regulation of gene activation by TOR.

DOI: 10.1128/MCB.00469-17
PubMed: 29712756
PubMed Central: PMC6024167


Affiliations:


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Le document en format XML

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<term>Genes, Fungal (MeSH)</term>
<term>Histone Acetyltransferases (genetics)</term>
<term>Histone Acetyltransferases (metabolism)</term>
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<term>Proteasome Endopeptidase Complex (metabolism)</term>
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<term>Protein-Serine-Threonine Kinases (metabolism)</term>
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<term>Ribosomal Proteins (metabolism)</term>
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<term>Saccharomyces cerevisiae (metabolism)</term>
<term>Saccharomyces cerevisiae Proteins (genetics)</term>
<term>Saccharomyces cerevisiae Proteins (metabolism)</term>
<term>Transcription Factor TFIID (genetics)</term>
<term>Transcription Factor TFIID (metabolism)</term>
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<term>Activation de la transcription (MeSH)</term>
<term>Adenosine triphosphatases (génétique)</term>
<term>Adenosine triphosphatases (métabolisme)</term>
<term>Facteur de transcription TFIID (génétique)</term>
<term>Facteur de transcription TFIID (métabolisme)</term>
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<term>Histone acetyltransferases (génétique)</term>
<term>Histone acetyltransferases (métabolisme)</term>
<term>Modèles biologiques (MeSH)</term>
<term>Mutation (MeSH)</term>
<term>Proteasome endopeptidase complex (génétique)</term>
<term>Proteasome endopeptidase complex (métabolisme)</term>
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<term>Protéines ribosomiques (métabolisme)</term>
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<term>Régulation de l'expression des gènes fongiques (MeSH)</term>
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<term>Saccharomyces cerevisiae (métabolisme)</term>
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<term>Proteasome Endopeptidase Complex</term>
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<term>Proteasome endopeptidase complex</term>
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<div type="abstract" xml:lang="en">TOR (target of rapamycin) has been previously implicated in transcriptional stimulation of the ribosomal protein (RP) genes via enhanced recruitment of NuA4 (nucleosome acetyltransferase of H4) to the promoters. However, it is not clearly understood how TOR enhances NuA4 recruitment to the promoters of the RP genes. Here we show that TOR facilitates the recruitment of the 19S proteasome subcomplex to the activator to enhance the targeting of NuA4 to the promoters of the RP genes. NuA4, in turn, promotes the recruitment of TFIID (transcription factor IID, composed of TATA box-binding protein [TBP] and a set of TBP-associated factors [TAFs]) and RNA polymerase II to the promoters of the RP genes to enhance transcriptional initiation. Therefore, our results demonstrate that TOR facilitates the recruitment of the 19S proteasome subcomplex to the promoters of the RP genes to promote the targeting of NuA4 for enhanced preinitiation complex (PIC) formation and consequently transcriptional initiation, hence illuminating TOR regulation of RP gene activation. Further, our results reveal that TOR differentially regulates PIC formation (and hence transcription) at the non-RP genes, thus demonstrating a complex regulation of gene activation by TOR.</div>
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