Genome-wide mapping of alternative splicing in Arabidopsis thaliana

被引:736
作者
Filichkin, Sergei A. [1 ,2 ]
Priest, Henry D. [1 ,2 ]
Givan, Scott A. [1 ,2 ]
Shen, Rongkun [1 ,2 ]
Bryant, Douglas W. [1 ,2 ,3 ]
Fox, Samuel E. [1 ,2 ]
Wong, Weng-Keen [3 ]
Mockler, Todd C. [1 ,2 ]
机构
[1] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[2] Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USA
[3] Oregon State Univ, Dept Elect Engn & Comp Sci, Corvallis, OR 97331 USA
关键词
MESSENGER-RNA DECAY; GENE; TRANSCRIPTOME; PROTEINS; SEQUENCE; ANNOTATION; EXPRESSION; PLANTS; RICE; IDENTIFICATION;
D O I
10.1101/gr.093302.109
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alternative splicing can enhance transcriptome plasticity and proteome diversity. In plants, alternative splicing can be manifested at different developmental stages, and is frequently associated with specific tissue types or environmental conditions such as abiotic stress. We mapped the Arabidopsis transcriptome at single-base resolution using the Illumina platform for ultrahigh-throughput RNA sequencing (RNA-seq). Deep transcriptome sequencing confirmed a majority of annotated introns and identified thousands of novel alternatively spliced mRNA isoforms. Our analysis suggests that at least similar to 42% of intron-containing genes in Arabidopsis are alternatively spliced; this is significantly higher than previous estimates based on cDNA/expressed sequence tag sequencing. Random validation confirmed that novel splice isoforms empirically predicted by RNA-seq can be detected in vivo. Novel introns detected by RNA-seq were substantially enriched in non-consensus terminal dinucleotide splice signals. Alternative isoforms with premature termination codons (PTCs) comprised the majority of alternatively spliced transcripts. Using an example of an essential circadian clock gene, we show that intron retention can generate relatively abundant PTC+ isoforms and that this specific event is highly conserved among diverse plant species. Alternatively spliced PTC+ isoforms can be potentially targeted for degradation by the nonsense mediated mRNA decay (NMD) surveillance machinery or regulate the level of functional transcripts by the mechanism of regulated unproductive splicing and translation (RUST). We demonstrate that the relative ratios of the PTC+ and reference isoforms for several key regulatory genes can be considerably shifted under abiotic stress treatments. Taken together, our results suggest that like in animals, NMD and RUST may be widespread in plants and may play important roles in regulating gene expression.
引用
收藏
页码:45 / 58
页数:14
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