| Literature DB >> 28137832 |
Shigeki Nagai1, Ralph E Davis1, Pierre Jean Mattei1, Kyle Patrick Eagen1, Roger D Kornberg2.
Abstract
Chromatin isolated from the chromosomal locus of the PHO5 gene of yeast in a transcriptionally repressed state was transcribed with 12 pure proteins (80 polypeptides): RNA polymerase II, six general transcription factors, TFIIS, the Pho4 gene activator protein, and the SAGA, SWI/SNF, and Mediator complexes. Contrary to expectation, a nucleosome occluding the TATA box and transcription start sites did not impede transcription but rather, enhanced it: the level of chromatin transcription was at least sevenfold greater than that of naked DNA, and chromatin gave patterns of transcription start sites closely similar to those occurring in vivo, whereas naked DNA gave many aberrant transcripts. Both histone acetylation and trimethylation of H3K4 (H3K4me3) were important for chromatin transcription. The nucleosome, long known to serve as a general gene repressor, thus also performs an important positive role in transcription.Entities:
Keywords: PHO5; RNA polymerase II; Saccharomyces cerevisiae
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Year: 2017 PMID: 28137832 PMCID: PMC5320956 DOI: 10.1073/pnas.1620312114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205