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Determination of local chromatin interactions using a combined CRISPR and peroxidase APEX2 system

ABSTRACT: The architecture and function of chromatin are largely regulated by local interacting molecules, such as transcription factors and noncoding RNAs. However, our understanding of these regulatory molecules at a given locus is limited because of technical difficulties. Here, we describe the use of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and an engineered ascorbate peroxidase 2 (APEX2) system to investigate local chromatin interactions (CAPLOCUS). We showed that with specific small-guide RNA targets, CAPLOCUS could efficiently identify both repetitive genomic regions and single-copy genomic locus with high resolution. Genome-wide sequencing revealed known and potential long-range chromatin interactions for a specific single-copy locus. CAPLOCUS also identified telomere-associated RNA. CAPLOCUS, followed by mass spectrometry, identified both known and novel telomere-associated proteins in their native states. Thus, CAPLOCUS may be a useful approach for studying local interacting molecules at any given chromosomal location.

ORGANISM(S): Homo sapiens

PROVIDER: GSE114133 | GEO | 2019/02/18

REPOSITORIES: GEO

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Determination of local chromatin interactions using a combined CRISPR and peroxidase APEX2 system

Project description:Determination of local chromatin interactions using a combined CRISPR and peroxidase APEX2 system

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