Analysis of Chromatin Interaction and Accessibility by Trac-Looping
Shuai Liu1, Qingsong Tang1, Keji Zhao2
1Laboratory of Epigenome Biology, Systems Biology Center, Division of Intramural Research, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Methods in Molecular Biology (Clifton, N.J.)
|February 22, 2023
Summary
We developed Trac-looping, a new method to study genome structure and cell activity by simultaneously detecting chromatin interactions and accessibility. This technique provides insights into how genome organization regulates biological processes.
Area of Science:
- Genomics
- Molecular Biology
- Epigenetics
Background:
- The spatial organization of the genome is crucial for regulating fundamental biological processes.
- Advancements in technology offer new perspectives on genome structure and its role in cellular functions.
- Understanding chromatin interactions and accessibility is key to deciphering gene regulation.
Purpose of the Study:
- To develop a novel method for analyzing genome-wide chromatin interactions specifically within accessible chromatin regions.
- To simultaneously assess both chromatin interactions and chromatin accessibility using a single, integrated technique.
Main Methods:
- Development of a DNA transposase-mediated analysis of chromatin looping (Trac-looping) method.
- Generation of Trac-looping libraries for high-throughput analysis.
- Detailed protocol description for library preparation and data acquisition.
Main Results:
- The Trac-looping method enables simultaneous detection of chromatin interactions and accessibility.
- This approach allows for the examination of genome-wide chromatin architecture at open chromatin sites.
- The protocol facilitates the generation of robust Trac-looping libraries.
Conclusions:
- Trac-looping is an effective method for studying the relationship between genome organization and cellular activity.
- This technique enhances our ability to investigate the functional implications of chromatin looping and accessibility.
- The described protocol provides a valuable tool for genomic research and understanding gene regulation.
Related Concept Videos
Chromatin Immunoprecipitation- ChIP
11.2K
Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
11.2K
Spreading of Chromatin Modifications
8.3K
The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
Writers
The writer...
8.3K


