@article{fce55928b344457990b0df45686bb8ec,
title = "FACT Remodels the Tetranucleosomal Unit of Chromatin Fibers for Gene Transcription",
abstract = "In eukaryotes, the packaging of genomic DNA into chromatin plays a critical role in gene regulation. However, the dynamic organization of chromatin fibers and its regulatory mechanisms remain poorly understood. Using single-molecule force spectroscopy, we reveal that the tetranucleosomes-on-a-string appears as a stable secondary structure during hierarchical organization of chromatin fibers. The stability of the tetranucleosomal unit is attenuated by histone chaperone FACT (facilitates chromatin transcription) in vitro. Consistent with in vitro observations, our genome-wide analysis further shows that FACT facilitates gene transcription by destabilizing the tetranucleosomal unit of chromatin fibers in yeast. Additionally, we found that the linker histone H1 not only enhances the stability but also facilitates the folding and unfolding kinetics of the outer nucleosomal wrap. Our study demonstrates that the tetranucleosome is a regulatory structural unit of chromatin fibers beyond the nucleosome and provides crucial mechanistic insights into the structure and dynamics of chromatin fibers during gene transcription.",
author = "Wei Li and Ping Chen and Juan Yu and Liping Dong and Dan Liang and Jianxun Feng and Jie Yan and Wang, {Peng Ye} and Qing Li and Zhiguo Zhang and Ming Li and Guohong Li",
note = "Funding Information: We are grateful to Drs. Bing Zhu, Pinchao Mei, Oliver Rando, Mingzhu Wang, and Rui-Ming Xu for critical reading and discussion of our manuscript. This work was supported by grants to G.L. from the Ministry of Science and Technology of China (2015CB856200), the National Natural Science Foundation of China (91219202, 31525013, and 31521002), and the Chinese Academy of Sciences (CAS) Strategic Priority Research Program (XDA01010304); to M.L. from the National Natural Science Foundation of China (61275192 and 11574382); to W.L. from National Natural Science Foundation of China (11474346) and the Ministry of Science and Technology of China (2013CB837200); to P.C. from the National Natural Science Foundation of China (31471218), the Key Research Program (KJZD-EW-L05), and the Youth Innovation Promotion Association CAS (2015071 to P.C.); to Z.Z. from the National Natural Science Foundation of China (31210103914); and to P.-Y.W. from the National Natural Science Foundation of China (11274374) and the National Key Research and Development Program (2016YFA0301500). The work was also supported by the CAS Interdisciplinary Innovation Team Program. All EM data were collected and processed at the Center for Bio-Imaging, Core Facility for Protein Sciences, Institute of Biophysics, and Chinese Academy of Sciences. We are also indebted to the colleagues whose work could not be cited because of the limitation of space. Publisher Copyright: {\textcopyright} 2016 Elsevier Inc.",
year = "2016",
month = oct,
day = "6",
doi = "10.1016/j.molcel.2016.08.024",
language = "English (US)",
volume = "64",
pages = "120--133",
journal = "Molecular Cell",
issn = "1097-2765",
publisher = "Cell Press",
number = "1",
}