Abstract
P>RNA-binding proteins are key regulators of plant gene expression. Consistent with this, the Arabidopsis genome encodes many RNA-binding proteins that are genetically required for normal development and for responding to environmental changes. However, the direct RNA targets and RNA processing events that these RNA-binding proteins control are poorly understood. In order to facilitate the functional characterization of RNA-binding proteins, we have applied the RNA immunoprecipitation assay to Arabidopsis. Working with the U2B '-U2 snRNA interaction as a model experimental system, we show that treatment of intact plants with formaldehyde allows immunocapture of U2 snRNA using antibodies that recognize U2B ' fused to the generic GFP tag. When coupled with recent developments in whole-genome tiling arrays and high-throughput next-generation sequencing, this combination of procedures and technology has the potential to allow systematic functional analysis of plant RNA-binding proteins.
Original language | English |
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Pages (from-to) | 163-168 |
Number of pages | 6 |
Journal | Plant Journal |
Volume | 59 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jul 2009 |
Keywords
- Arabidopsis
- post-transcriptional
- RNA-binding protein
- RNA immunoprecipitation
- RNA
- BINDING PROTEINS
- MESSENGER-RNA
- FLOWERING TIME
- THALIANA
- METHYLATION
- SPECIFICITY
- ENCODES
- BRAIN