Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017:1468:1-9.
doi: 10.1007/978-1-4939-4035-6_1.

Cellular Fractionation and Isolation of Chromatin-Associated RNA

Affiliations

Cellular Fractionation and Isolation of Chromatin-Associated RNA

Thomas Conrad et al. Methods Mol Biol. 2017.

Abstract

In eukaryotic cells, the synthesis, processing, and functions of RNA molecules are confined to distinct subcellular compartments. Biochemical fractionation of cells prior to RNA isolation thus enables the analysis of distinct steps in the lifetime of individual RNA molecules that would be masked in bulk RNA preparations from whole cells. Here, we describe a simple two-step differential centrifugation protocol for the isolation of cytoplasmic, nucleoplasmic, and chromatin-associated RNA that can be used in downstream applications such as qPCR or deep sequencing. We discuss various aspects of this fractionation protocol, which can be readily applied to many mammalian cell types. For the study of long noncoding RNAs and enhancer RNAs in regulation of transcription especially the preparation of chromatin-associated RNA can contribute significantly to further developments.

Keywords: Cellular fractionation; Chromatin–RNA; Enhancer RNA; Long noncoding RNA; Nascent RNA; Primary transcripts; RNA nuclear export; RNA processing; RNA splicing; RNA subcellular localization.

PubMed Disclaimer

Similar articles

Cited by

LinkOut - more resources