Spatial mapping of splicing factor complexes involved in exon and intron definition

Jonathan D. Ellis, David Llères, Marco Denegri, Angus I. Lamond, Javier F. Cáceres

Research output: Contribution to journalArticle

Abstract

We have analyzed the interaction between serine/arginine-rich (SR) proteins and splicing components that recognize either the 5′ or 3′ splice site. Previously, these interactions have been extensively characterized biochemically and are critical for both intron and exon definition. We use fluorescence resonance energy transfer (FRET) microscopy to identify interactions of individual SR proteins with the U1 small nuclear ribonucleoprotein (snRNP)-associated 70-kD protein (U1 70K) and with the small subunit of the U2 snRNP auxiliary factor (U2AF35) in live-cell nuclei. We find that these interactions occur in the presence of RNA polymerase II inhibitors, demonstrating that they are not exclusively cotranscriptional. Using FRET imaging by means of fluorescence lifetime imaging microscopy (FLIM), we map these interactions to specific sites in the nucleus. The FLIM data also reveal a previously unknown interaction between HCC1, a factor related to U2AF65, with both subunits of U2AF. Spatial mapping using FLIM-FRET reveals differences in splicing factors interactions within complexes located in separate subnuclear domains.

Original languageEnglish
Pages (from-to)921-934
Number of pages14
JournalJournal of Cell Biology
Volume181
Issue number6
DOIs
Publication statusPublished - Jun 16 2008

ASJC Scopus subject areas

  • Cell Biology

Fingerprint Dive into the research topics of 'Spatial mapping of splicing factor complexes involved in exon and intron definition'. Together they form a unique fingerprint.

  • Cite this