Super enhancers—Functional cores under the 3D genome
Complex biochemical reactions take place in the nucleus all the time. Transcription machines must follow the rules. The chromatin state, especially the three‐dimensional structure of the genome, plays an important role in gene regulation and expression. The super enhancers are important for defining...
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Published in | Cell proliferation Vol. 54; no. 2; pp. e12970 - n/a |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.02.2021
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Complex biochemical reactions take place in the nucleus all the time. Transcription machines must follow the rules. The chromatin state, especially the three‐dimensional structure of the genome, plays an important role in gene regulation and expression. The super enhancers are important for defining cell identity in mammalian developmental processes and human diseases. It has been shown that the major components of transcriptional activation complexes are recruited by super enhancer to form phase‐separated condensates. We summarize the current knowledge about super enhancer in the 3D genome. Furthermore, a new related transcriptional regulation model from super enhancer is outlined to explain its role in the mammalian cell progress.
As a regulatory element on the genome, the formation of super enhancers depends on specific chromatin states and spatial structures. A large number of regulatory molecules gather in the chromatin regions where the super enhancers are located. The molecules in these regions are very dense, forming huge transcriptional activation complexes, which interact with each other to construct phase‐separated condensates. Super enhancer‐mediated transcriptional activation depends on spatial proximity rather than a rigid bridge. There are molecular exchanges between the super enhancer‐associated condensate and the surroundings. Inactive Pol II is recruited and phosphorylated Pol II is excreted. Therefore, we propose a super enhancer‐mediated transcription mode to pave the way for future research. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Funding informationThis work was supported by grants from the Program of National Natural Science Foundation of China (31572399, 32072806, The National Key Research and Development Program of China, Stem Cell and Translational Research (Grant No. 2016YFA0100203), Program of Shaanxi Province Science and Technology Innovation Team (2019TD‐036), Swedish Research Council (VR‐2016‐06794, VR‐2017‐02074 to XC), Beijer Foundation, Jeassons Foundation, Petrus och Augusta Hedlunds Stiftelse (To XC), Göran Gustafsson's prize for younger researchers (To XC), Vleugel Foundation (To XC), Beijer Foundation (To XC) and Uppsala University (To XC) |
ISSN: | 0960-7722 1365-2184 1365-2184 |
DOI: | 10.1111/cpr.12970 |