Unknown

Dataset Information

0

BL-Hi-C is an efficient and sensitive approach for capturing structural and regulatory chromatin interactions.


ABSTRACT: In human cells, DNA is hierarchically organized and assembled with histones and DNA-binding proteins in three dimensions. Chromatin interactions play important roles in genome architecture and gene regulation, including robustness in the developmental stages and flexibility during the cell cycle. Here we propose in situ Hi-C method named Bridge Linker-Hi-C (BL-Hi-C) for capturing structural and regulatory chromatin interactions by restriction enzyme targeting and two-step proximity ligation. This method improves the sensitivity and specificity of active chromatin loop detection and can reveal the regulatory enhancer-promoter architecture better than conventional methods at a lower sequencing depth and with a simpler protocol. We demonstrate its utility with two well-studied developmental loci: the beta-globin and HOXC cluster regions.

SUBMITTER: Liang Z 

PROVIDER: S-EPMC5696378 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

BL-Hi-C is an efficient and sensitive approach for capturing structural and regulatory chromatin interactions.

Liang Zhengyu Z   Li Guipeng G   Wang Zejun Z   Djekidel Mohamed Nadhir MN   Li Yanjian Y   Qian Min-Ping MP   Zhang Michael Q MQ   Chen Yang Y  

Nature communications 20171120 1


In human cells, DNA is hierarchically organized and assembled with histones and DNA-binding proteins in three dimensions. Chromatin interactions play important roles in genome architecture and gene regulation, including robustness in the developmental stages and flexibility during the cell cycle. Here we propose in situ Hi-C method named Bridge Linker-Hi-C (BL-Hi-C) for capturing structural and regulatory chromatin interactions by restriction enzyme targeting and two-step proximity ligation. Thi  ...[more]

Similar Datasets

2018-01-23 | GSE93921 | GEO
| S-EPMC7441592 | biostudies-literature
| S-EPMC6838123 | biostudies-literature
| S-EPMC4032863 | biostudies-literature
2019-09-30 | GSE136756 | GEO
| S-EPMC5442359 | biostudies-literature