| Literature DB >> 29501423 |
Silvia Kocanova1, Isabelle Goiffon2, Kerstin Bystricky3.
Abstract
Fluorescence in situ hybridization (FISH) is a common technique used to label DNA and/or RNA for detection of a genomic region of interest. However, the technique can be challenging, in particular when applied to single genes in human cancer cells. Here, we provide a step-by-step protocol for analysis of short (35 kb-300 kb) genomic regions in three dimensions (3D). We discuss the experimental design and provide practical considerations for 3D imaging and data analysis to determine chromatin folding. We demonstrate that 3D FISH using BACs (Bacterial Artificial Chromosomes) or fosmids can provide detailed information of the architecture of gene domains. More specifically, we show that mapping of specific chromatin landscapes informs on changes associated with estrogen stimulated gene activity in human breast cancer cell lines.Entities:
Keywords: Breast cancer cells; Chromatin folding; Estrogen-regulated genes; Fluorescence in situ hybridization; Fluorescence microscopy; Genome architecture
Mesh:
Substances:
Year: 2018 PMID: 29501423 DOI: 10.1016/j.ymeth.2018.02.013
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608