scholarly journals WAPL maintains a cohesin loading cycle to preserve cell-type-specific distal gene regulation

2020 ◽  
Vol 53 (1) ◽  
pp. 100-109
Author(s):  
Ning Qing Liu ◽  
Michela Maresca ◽  
Teun van den Brand ◽  
Luca Braccioli ◽  
Marijne M. G. A. Schijns ◽  
...  
2021 ◽  
Vol 89 (9) ◽  
pp. S25
Author(s):  
Dan Liang ◽  
Nil Aygün ◽  
Angela Elwell ◽  
Oleh Krupa ◽  
Felix Kyere ◽  
...  

2019 ◽  
Author(s):  
Cheynna Crowley ◽  
Yuchen Yang ◽  
Yunjiang Qiu ◽  
Benxia Hu ◽  
Armen Abnousi ◽  
...  

AbstractHi-C experiments have been widely adopted to study chromatin spatial organization, which plays an essential role in genome function. We have recently identified frequently interacting regions (FIREs) and found that they are closely associated with cell-type-specific gene regulation. However, computational tools for detecting FIREs from Hi-C data are still lacking. In this work, we present FIREcaller, a stand-alone, user-friendly R package for detecting FIREs from Hi-C data. FIREcaller takes raw Hi-C contact matrices as input, performs within-sample and cross-sample normalization, and outputs continuous FIRE scores, dichotomous FIREs, and super-FIREs. Applying FIREcaller to Hi-C data from various human tissues, we demonstrate that FIREs and super-FIREs identified, in a tissue-specific manner, are closely related to gene regulation, are enriched for enhancer-promoter (E-P) interactions, tend to overlap with regions exhibiting epigenomic signatures of cis-regulatory roles, and aid the interpretation or GWAS variants. The FIREcaller package is implemented in R and freely available at https://yunliweb.its.unc.edu/FIREcaller.Highlights– Frequently Interacting Regions (FIREs) can be used to identify tissue and cell-type-specific cis-regulatory regions.– An R software, FIREcaller, has been developed to identify FIREs and clustered FIREs into super-FIREs.


PLoS ONE ◽  
2011 ◽  
Vol 6 (11) ◽  
pp. e27770 ◽  
Author(s):  
Yi Tian ◽  
Zhengcai Jia ◽  
Jun Wang ◽  
Zemin Huang ◽  
Jun Tang ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (2) ◽  
pp. e31416 ◽  
Author(s):  
Licheng Ren ◽  
Yang Wang ◽  
Minglei Shi ◽  
Xiaoning Wang ◽  
Zhong Yang ◽  
...  

2004 ◽  
Vol 356 (2) ◽  
pp. 107-110 ◽  
Author(s):  
Minori Dateki ◽  
Reiko Mochizuki ◽  
Kazuyuki Yanai ◽  
Akiyoshi Fukamizu

2018 ◽  
Author(s):  
Jayoung Ryu ◽  
Hyunwoong Kim ◽  
Dongchan Yang ◽  
Andrew J. Lee ◽  
Inkyung Jung

AbstractSuper-enhancers or stretch enhancers are clusters of active enhancers that often coordinate cell-type specific gene regulation. However, little is known about the function of super-enhancers beyond gene regulation. In this study, through a comprehensive analysis of super-enhancers in 30 human cell/tissue types, we identified a new class of super-enhancers which are constitutively active across most cell/tissue types. These ‘common’ super-enhancers are associated with universally highly expressed genes in contrast to the canonical definition of super-enhancers that assert cell-type specific gene regulation. In addition, the genome sequence of these super-enhancers is highly conserved by evolution and among humans, advocating their universal function in genome regulation. Integrative analysis of 3D chromatin loops demonstrates that, in comparison to the cell-type specific super-enhancers, the cell-type common super-enhancers present a striking association with rapidly recovering loops. We propose that a new class of super-enhancers may play an important role in the early establishment of 3D chromatin structure.BackgroundSuper-enhancers or stretch enhancers are defined by a strong enrichment of mediators and transcription-regulating proteins, appearing to play a deterministic role in cellular identity by controlling the expression of cell-type specific genes[1, 2]. Previous studies have revealed the critical function of super-enhancers during development and differentiation[3]. The enrichment of disease-associated single nucleotide polymorphism (SNP) in super-enhancers compared to that of typical enhancers proposed a substantial link between super-enhancers and many complex human diseases[2]. In addition, a set of recent studies have proposed potential functions of super-enhancers in the extremely long-range chromatin communications and the establishment of 3D chromatin loops[4]. These results suggest a more universal role of super-enhancers in genome regulation apart from cell-type specific gene regulation, but little is known about the mechanisms underlying these various functions. To extend the current knowledge of super-enhancers and their biological roles, we conducted a comprehensive analysis of super-enhancer activities across 30 human cell/tissue types. Our analysis suggests that a substantial number of super-enhancers exhibits prevalent activities across cell-types in terms of H3K27ac signals, and that these non-canonical super-enhancers are involved in the formation of fast recovering chromatin loops.NoteA genome browser session has been set up for visualization of the super-enhancer domains described in the current study– https://genome.ucsc.edu/cgi-bin/hgTracks?hgS-doOtherUser=submit&hgS-otherUserName=abundantiavosliberabit&hgS-otherUserSessionName=SuperEnhancerDomain


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