| Literature DB >> 34286007 |
Mauricio A Reynoso1, Germain C Pauluzzi1, Sean Cabanlit1, Joel Velasco1, Jérémie Bazin2, Roger Deal3, Siobhan Brady4,5, Neelima Sinha4, Julia Bailey-Serres1, Kaisa Kajala4,5.
Abstract
Gene expression is dynamically regulated on many levels, including chromatin accessibility and transcription. In order to study these nuclear regulatory events, we describe our method to purify nuclei with Isolation of Nuclei in TAgged Cell Types (INTACT). As nuclear RNA is low in polyadenylated transcripts and conventional pulldown methods would not capture non-polyadenylated pre-mRNA, we also present our method to remove ribosomal RNA from the total nuclear RNA in preparation for nuclear RNA-Seq.Entities:
Keywords: Gene expression; INTACT; Nuclear purification; RNA extraction; RNA-Seq; rRNA degradation
Year: 2018 PMID: 34286007 PMCID: PMC8275268 DOI: 10.21769/BioProtoc.2458
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325