Nucleosomal Elements that Control the Topography of the Barrier to Transcription
Open accessAbstract
The nucleosome represents a mechanical barrier to transcription that operates as a general regulator of gene expression. We investigate how each nucleosomal component-the histone tails, the specific histone-DNA contacts, and the DNA sequence-contributes to the strength of the barrier. Removal of the tails favors progression of RNA polymerase II into the entry region of the nucleosome by locally increasing the wrapping-unwrapping rates of the DNA around histones. In contrast, point mutations that affect histone-DNA contacts at the dyad abolish the barrier to transcription in the central region by decreasing the local wrapping rate. Moreover, we show that the nucleosome amplifies sequence-dependent transcriptional pausing, an effect mediated through the structure of the nascent RNA. Each of these nucleosomal elements controls transcription elongation by affecting distinctly the density and duration of polymerase pauses, thus providing multiple and alternative mechanisms for control of gene expression by chromatin remodeling and transcription factors.
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Nucleosomes can induce RNA Pol II pausing in vitro and in vivo and may even be the major source of pausing.
“Nucleosomes can induce RNA Pol II pausing in vitro and in vivo and may even be the major source of pausing (Churchman & Weissman, 2011; Bintu et al, 2012).”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Bintu et al, 2012
The Results section, “The Histone Tails Gate the Nucleosome Entry” (page unavailable), reports increased Pol II pausing with nucleosomes compared with bare DNA, supporting the in vitro portion. The passages found do not establish nucleosome-induced pausing in vivo or suggest that nucleosomes are the major source of pausing. (LLM, conf=0.87)
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References 49 · Cited by 192
- Authors
- Bintu, L., Ishibashi, T., Dangkulwanich, M., Wu, Y.-Y., Lubkowska, L., Kashlev, M., & Bustamante, C.
- Affiliations
- University of California, Berkeley (US)
- Center for Cancer Research (US)
- QB3 (US)
- Corresponding author
- Bustamante, Carlos
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2012-11
- Volume
- 151
- Issue
- 4
- Pages
- 738-749
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3508686
- OpenAlex
- W2006855885
- Cited by
- 192
- References
- 49
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 12 · 2023: 9 · 2022: 18 · 2021: 12 · 2020: 13 · 2019: 13 · 2018: 13 · 2017: 14 · 2016: 20 · 2015: 15 · 2014: 17 · 2013: 22
- FWCI
- 6.94
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Rare & Special e-Zone (The Hong Kong University of Science and Technology) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute of General Medical Sciences (R01-GM032543-31, R01GM032543)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- nucleosome, RNA polymerase II, histone tails, histone-DNA interactions, nucleosome dyad, transcriptional pausing, transcription elongation, chromatin remodeling, gene expression regulation
- MeSH terms
- DNA, Gene Expression Regulation, Histones, Nucleosomes, RNA Polymerase II, Transcription, Genetic, Yeasts
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