RNA-Binding Protein-Mediated mRNA Deadenylation in Mammalian Cell Extracts

Methods Mol Biol. 2024:2723:173-191. doi: 10.1007/978-1-0716-3481-3_11.

Abstract

Removal of the poly(A) tail, or deadenylation, is a crucial step in destabilizing mRNAs in eukaryotes. In this chapter, we describe a cell-free deadenylation assay that uses cytoplasmic cell extracts from human HEK293 cells transiently transfected with DNA encoding RNA-binding proteins (RBP), and in vitro-transcribed, radiolabeled, RNA probes. We include methods to evaluate the effects of RBPs or deadenylases on various in vitro-transcribed probes, with or without poly(A) tails. Finally, we also demonstrate the adaptability of these assays to test purified protein components in our cell-free deadenylation assay. In our experience, these methods are well suited for the initial assessment of the effects of RBPs on the deadenylation of mRNAs.

Keywords: Capped RNA probes; Cytosolic extracts; Deadenylation; Poly(A); mRNA-binding proteins (RBPs).

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cell Extracts
  • HEK293 Cells
  • Humans
  • Mammals / genetics
  • Poly A / metabolism
  • RNA Stability
  • RNA*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins* / metabolism

Substances

  • Cell Extracts
  • RNA, Messenger
  • RNA-Binding Proteins
  • RNA
  • Poly A