scholarly journals Histone H5-chromatin interactions in situ are strongly modulated by H5 C-terminal phosphorylation

2012 ◽  
Vol 83A (3) ◽  
pp. 273-279 ◽  
Author(s):  
Nora N. Kostova ◽  
Ljuba Srebreva ◽  
Dimiter V. Markov ◽  
Bettina Sarg ◽  
Herbert H. Lindner ◽  
...  
Cell ◽  
2017 ◽  
Vol 170 (5) ◽  
pp. 1028-1043.e19 ◽  
Author(s):  
Xin Liu ◽  
Yuannyu Zhang ◽  
Yong Chen ◽  
Mushan Li ◽  
Feng Zhou ◽  
...  

2021 ◽  
Author(s):  
Yuxiao Zhou ◽  
Siyuan Xu ◽  
Qiang Wu

Enhancers generate bidirectional noncoding enhancer RNAs that may regulate gene expression. At present, mechanisms of eRNA functions are not fully understood. Here, we report an antisense eRNA PEARL that is transcribed from the protocadherin α HS5-1 enhancer region. Through loss- and gain-of-function experiments with CRISPR/Cas9 DNA-fragment editing, CRISPRi, and CRISPRa strategies, in conjunction with ChIRP, MeDIP, and DRIP experiments, we find that PEARL regulates Pcdhα expression by forming local R-loop in situ within the HS5-1 enhancer region to promote long-distance chromatin interactions between distal enhancer and target promoters. These findings have important implications regarding mechanisms by which the HS5-1 enhancer regulates stochastic Pcdhα promoter choice in single cells in the brain.


Chromosoma ◽  
1996 ◽  
Vol 104 (7) ◽  
pp. 504-510 ◽  
Author(s):  
Jian-Min Sun ◽  
Rosa Ferraiuolo ◽  
James R. Davie

2019 ◽  
Author(s):  
Xu Zhang ◽  
Jing Niu ◽  
Guipeng Li ◽  
Qionghai Dai ◽  
Dayong Jin ◽  
...  

ABSTRACTThere is increasing interest in understanding how the three-dimensional organization of the genome is regulated. Different strategies have been employed to identify chromatin interactions genome wide. However, due to the current limitations in resolving genomic contacts, visualization and validation of these genomic loci with sub-kilobase resolution remain the bottleneck for many years. Here, we describe Tn5 transposase-based Fluorescence in situ Hybridization (Tn5-FISH), a Polymerase Chain Reaction (PCR)-based, cost-effective imaging method, which achieved the co-localization of genomic loci with sub-kilobase resolution, to fine dissect genome architecture at sub-kilobase resolution and to verify chromatin interactions detected by Chromatin Configuration Capture (3C)-derivative methods. Especially, Tn5-FISH is very useful to verify short-range chromatin interactions inside of contact domain and Topologically Associated Domain (TAD). It also offers one powerful molecular diagnosis tool for clinical detection of cytogenetic changes in cancers.


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