Transcription initiation platforms and GTF recruitment at tissue-specific enhancers and promoters.

Koch F, Fenouil R, Gut M, Cauchy P, Albert TK, Zacarias-Cabeza J, Spicuglia S, de la Chapelle AL, Heidemann M, Hintermair C, Eick D, Gut I, Ferrier P, Andrau JC

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Recent work has shown that RNA polymerase (Pol) II can be recruited to and transcribe distal regulatory regions. Here we analyzed transcription initiation and elongation through genome-wide localization of Pol II, general transcription factors (GTFs) and active chromatin in developing T cells. We show that Pol II and GTFs are recruited to known T cell-specific enhancers. We extend this observation to many new putative enhancers, a majority of which can be transcribed with or without polyadenylation. Importantly, we also identify genomic features called transcriptional initiation platforms (TIPs) that are characterized by large areas of Pol II and GTF recruitment at promoters, intergenic and intragenic regions. TIPs show variable widths (0.4-10 kb) and correlate with high CpG content and increased tissue specificity at promoters. Finally, we also report differential recruitment of TFIID and other GTFs at promoters and enhancers. Overall, we propose that TIPs represent important new regulatory hallmarks of the genome.

Details zur Publikation

FachzeitschriftNature Structural and Molecular Biology (Nat Struct Mol Biol)
Jahrgang / Bandnr. / Volume18
Ausgabe / Heftnr. / Issue8
Seitenbereich956-963
StatusVeröffentlicht
Veröffentlichungsjahr2011
Sprache, in der die Publikation verfasst istEnglisch
StichwörterPolyadenylation; DNA. Promoter Regions Genetic; Transcription Factors General; CpG Islands; RNA Polymerase II. Animals; Enhancer Elements Genetic; Transcription Initiation Site; Mice; Polyadenylation; DNA. Promoter Regions Genetic; Transcription Factors General; CpG Islands; RNA Polymerase II. Animals; Enhancer Elements Genetic; Transcription Initiation Site; Mice

Autor*innen der Universität Münster

Albert, Thomas
Institut für Molekulare Tumorbiologie