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Transition from initiation to promoter proximal pausing requires the CTD of RNA polymerase II.

Nucleic Acids Res. 33, 5139-5144 (2005)
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The C-terminal domain (CTD) of mammalian RNA polymerase II consists of 52 repeats of the consensus hepta-peptide YSPTSPS, and links transcription to the processing of pre-mRNA. Although Pol II with a CTD shortened to five repeats (Pol II Delta5) is transcriptionally inactive on chromatin templates, it is not clear whether CTD is required for promoter recognition in vivo. Here, we demonstrate that in the context of chromatin, Pol II Delta5 can bind to the c-myc promoter with the same efficiency as wild type Pol II. However, Pol II Delta5 does not form a stable initiation complex, and does not transcribe promoter proximal sequences. Fluorescence recovery after photobleaching (FRAP) experiments with cells expressing enhanced green fluorescent protein (EGFP)-tagged Delta5 or wildtype Pol II revealed a single, highly mobile Pol II Delta5 fraction whereas wildtype Pol II yielded less mobile fractions. These data suggest that CTD is not required for promoter recognition, but rather for subsequent formation of a stable initiation complex and isomerization to an elongation competent complex.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter CARBOXYL-TERMINAL DOMAIN; BURKITTS-LYMPHOMA CELLS; MAMMALIAN-CELLS; LARGEST SUBUNIT; PHOSPHORYLATION; TRANSCRIPTION; KINASES; EXPRESSION; STABILITY; COMPLEX
ISSN (print) / ISBN 0305-1048
e-ISSN 1362-4962
Quellenangaben Band: 33, Heft: 16, Seiten: 5139-5144 Artikelnummer: , Supplement: ,
Verlag Oxford University Press
Begutachtungsstatus