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Identification of novel functional TBP-binding sites and general factor repertoires.


ABSTRACT: Our current knowledge of the general factor requirement in transcription by the three mammalian RNA polymerases is based on a small number of model promoters. Here, we present a comprehensive chromatin immunoprecipitation (ChIP)-on-chip analysis for 28 transcription factors on a large set of known and novel TATA-binding protein (TBP)-binding sites experimentally identified via ChIP cloning. A large fraction of identified TBP-binding sites is located in introns or lacks a gene/mRNA annotation and is found to direct transcription. Integrated analysis of the ChIP-on-chip data and functional studies revealed that TAF12 hitherto regarded as RNA polymerase II (RNAP II)-specific was found to be also involved in RNAP I transcription. Distinct profiles for general transcription factors and TAF-containing complexes were uncovered for RNAP II promoters located in CpG and non-CpG islands suggesting distinct transcription initiation pathways. Our study broadens the spectrum of general transcription factor function and uncovers a plethora of novel, functional TBP-binding sites in the human genome.

SUBMITTER: Denissov S 

PROVIDER: S-EPMC1852848 | biostudies-literature | 2007 Feb

REPOSITORIES: biostudies-literature

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Identification of novel functional TBP-binding sites and general factor repertoires.

Denissov Sergey S   van Driel Marc M   Voit Renate R   Hekkelman Maarten M   Hulsen Tim T   Hernandez Nouria N   Grummt Ingrid I   Wehrens Ron R   Stunnenberg Hendrik H  

The EMBO journal 20070201 4


Our current knowledge of the general factor requirement in transcription by the three mammalian RNA polymerases is based on a small number of model promoters. Here, we present a comprehensive chromatin immunoprecipitation (ChIP)-on-chip analysis for 28 transcription factors on a large set of known and novel TATA-binding protein (TBP)-binding sites experimentally identified via ChIP cloning. A large fraction of identified TBP-binding sites is located in introns or lacks a gene/mRNA annotation and  ...[more]

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