Evidence map›Paper›PMID 25652661›Full record

ArticleBMC plant biology2015

Comparative genomics of grass EST libraries reveals previously uncharacterized splicing events in crop plants.

Trees-Juen Chuang, Min-Yu Yang, Chuang-Chieh Lin, Ping-Hung Hsieh, Li-Yuan Hung

Abstract read
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Article in BMC plant biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Trees-Juen ChuangGenomics Research Center, Academia Sinica, Taipei, 11529, Taiwan. trees@gate.sinica.edu.tw.
Min-Yu YangGenomics Research Center, Academia Sinica, Taipei, 11529, Taiwan. koineyang@gmail.com.
Chuang-Chieh LinGenomics Research Center, Academia Sinica, Taipei, 11529, Taiwan. josephcclin@iis.sinica.edu.tw.
Ping-Hung HsiehGenomics Research Center, Academia Sinica, Taipei, 11529, Taiwan. r94623005@gmail.com.
Li-Yuan HungGenomics Research Center, Academia Sinica, Taipei, 11529, Taiwan. oro@csie.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCrop plants such as rice, maize and sorghum play economically-important roles as main sources of food, fuel, and animal feed. However, current genome annotations of crop plants still suffer false-positive predictions; a more comprehensive registry of alternative splicing (AS) events is also in demand. Comparative genomics of crop plants is largely unexplored.

resultsWe performed a large-scale comparative analysis (ExonFinder) of the expressed sequence tag (EST) library from nine grass plants against three crop genomes (rice, maize, and sorghum) and identified 2,879 previously-unannotated exons (i.e., novel exons) in the three crops. We validated 81% of the tested exons by RT-PCR-sequencing, supporting the effectiveness of our in silico strategy. Evolutionary analysis reveals that the novel exons, comparing with their flanking annotated ones, are generally under weaker selection pressure at the protein level, but under stronger pressure at the RNA level, suggesting that most of the novel exons also represent novel alternatively spliced variants (ASVs). However, we also observed the consistency of evolutionary rates between certain novel exons and their flanking exons, which provided further evidence of their co-occurrence in the transcripts, suggesting that previously-annotated isoforms might be subject to erroneous predictions. Our validation showed that 54% of the tested genes expressed the newly-identified isoforms that contained the novel exons, rather than the previously-annotated isoforms that excluded them. The consistent results were steadily observed across cultivated (Oryza sativa and O. glaberrima) and wild (O. rufipogon and O. nivara) rice species, asserting the necessity of our curation of the crop genome annotations. Our comparative analyses also inferred the common ancestral transcriptome of grass plants and gain- and loss-of-ASV events.

conclusionsWe have reannotated the rice, maize, and sorghum genomes, and showed that evolutionary rates might serve as an indicator for determining whether the identified exons were alternatively spliced. This study not only presents an effective in silico strategy for the improvement of plant annotations, but also provides further insights into the role of AS events in the evolution and domestication of crop plants. ExonFinder and the novel exons/ASVs identified are publicly accessible at http://exonfinder.sourceforge.net/ .

Indexed as

Genome, PlantAlternative SplicingCrops, AgriculturalExonsExpressed Sequence TagsOryzaPlant ProteinsPoaceaeProtein IsoformsReal-Time Polymerase Chain ReactionSorghumZea maysPlant ProteinsProtein Isoforms

Identifiers

PMID25652661
PMCPMC4323234

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.