A protocol for imaging alternative splicing regulation in vivo using fluorescence reporters in transgenic mice.

Journal Article

Imaging technologies are influencing the way we study regulatory processes in vivo. Several recent reports use fluorescence minigenes to image alternative splicing events in living cells and animals. This type of reporter is being used to generate transgenic mice to visualize splicing regulation in diverse tissues and cell types. In this protocol, we describe how to develop animals that report on alternative splicing and how to assess reporter expression in excised organs and tissue sections. The entire procedure, from making the reporters to imaging organs and tissues in adult transgenic mice, should take approximately 1.5 years. Fluorescence reporters can be used to image many splicing decisions in normal tissues and organs and can be extended to the study of disease states.

Full Text

Duke Authors

Cited Authors

  • Bonano, VI; Oltean, S; Garcia-Blanco, MA

Published Date

  • 2007

Published In

Volume / Issue

  • 2 / 9

Start / End Page

  • 2166 - 2181

PubMed ID

  • 17853873

Electronic International Standard Serial Number (EISSN)

  • 1750-2799

Digital Object Identifier (DOI)

  • 10.1038/nprot.2007.292

Language

  • eng

Conference Location

  • England