Nucleosome destabilization by nuclear non-coding RNAs

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作者
Risa Fujita
Tatsuro Yamamoto
Yasuhiro Arimura
Saori Fujiwara
Hiroaki Tachiwana
Yuichi Ichikawa
Yuka Sakata
Liying Yang
Reo Maruyama
Michiaki Hamada
Mitsuyoshi Nakao
Noriko Saitoh
Hitoshi Kurumizaka
机构
[1] The University of Tokyo,Laboratory of Chromatin Structure and Function, Institute for Quantitative Biosciences
[2] Kumamoto University,Department of Medical Cell Biology, Institute of Molecular Embryology and Genetics
[3] Division of Cancer Biology,Graduate School of Advanced Science and Engineering
[4] The Cancer Institute of Japanese Foundation for Cancer Research,undefined
[5] Project for Cancer Epigenomics,undefined
[6] The Cancer Institute of Japanese Foundation for Cancer Research,undefined
[7] Waseda University,undefined
[8] AIST-Waseda University Computational Bio Big-Data Open Innovation Laboratory (CBBD-OIL),undefined
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Communications Biology | / 3卷
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摘要
In the nucleus, genomic DNA is wrapped around histone octamers to form nucleosomes. In principle, nucleosomes are substantial barriers to transcriptional activities. Nuclear non-coding RNAs (ncRNAs) are proposed to function in chromatin conformation modulation and transcriptional regulation. However, it remains unclear how ncRNAs affect the nucleosome structure. Eleanors are clusters of ncRNAs that accumulate around the estrogen receptor-α (ESR1) gene locus in long-term estrogen deprivation (LTED) breast cancer cells, and markedly enhance the transcription of the ESR1 gene. Here we detected nucleosome depletion around the transcription site of Eleanor2, the most highly expressed Eleanor in the LTED cells. We found that the purified Eleanor2 RNA fragment drastically destabilized the nucleosome in vitro. This activity was also exerted by other ncRNAs, but not by poly(U) RNA or DNA. The RNA-mediated nucleosome destabilization may be a common feature among natural nuclear RNAs, and may function in transcription regulation in chromatin.
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