Abstract

Alternative splicing plays a major role in expanding the potential informational content of eukaryotic genomes. It is an important post-transcriptional regulatory mechanism that can increase protein diversity and affect mRNA stability. Alternative splicing is often regulated in a tissue-specific and stress-responsive manner. Cold stress, which adversely affects plant growth and development, regulates the transcription and splicing of plant splicing factors. This can affect the pre-mRNA processing of many genes. To identify cold regulated alternative splicing we applied Affymetrix Arabidopsis tiling arrays to survey the transcriptome under cold treatment conditions. A novel algorithm was used for detection of statistically relevant changes in intron expression within a transcript between control and cold growth conditions. A reverse transcription polymerase chain reaction (RT-PCR) analysis of a number of randomly selected genes confirmed the changes in splicing patterns under cold stress predicted by tiling array. Our analysis revealed new types of cold responsive genes. While their expression level remains relatively unchanged under cold stress their splicing pattern shows detectable changes in the relative abundance of isoforms. The majority of cold regulated alternative splicing introduced a premature termination codon (PTC) into the transcripts creating potential targets for degradation by the nonsense mediated mRNA decay (NMD) process. A number of these genes were analyzed in NMD-defective mutants by RT-PCR and shown to evade NMD. This may result in new and truncated proteins with altered functions or dominant negative effects. The results indicate that cold affects both quantitative and qualitative aspects of gene expression.

Highlights

  • Plants are sessile organisms and as such are unable to escape from harsh environmental conditions

  • Mapping Affymetrix probes to the Arabidopsis genome Transcriptome analysis using Whole-genome tiling arrays (WGA) was explored for its ability to define splicing events regulated by cold

  • The method developed for the detection of alternatively spliced introns is based on differences in intron probes expression level between control and cold stress treatments and was applied to analyze changes in alternative splicing in Arabidopsis after cold treatment

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Summary

Introduction

Plants are sessile organisms and as such are unable to escape from harsh environmental conditions. Plants have evolved a variety of mechanisms to cope with these stresses, including stress-regulated transcriptional responses that lead to biochemical and physiological changes [1,2,3,4]. Cold stress is one of the major environmental factors that adversely affects plants’ growth and development, and limits crops geographical distribution and yield. The expression and splicing of many serine/arginine-rich (SR) genes, which encode splicing factor proteins that are essential for constitutive and alternative splicing [16], change under cold stress [4,6,17,18]. Since cold stress alters the expression of splicing factors it affects the splicing of precursor-mRNAs (pre-mRNA) of other genes, which may have an adaptive significance

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