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ARS Home » Pacific West Area » Albany, California » Plant Gene Expression Center » Research » Publications at this Location » Publication #296904
Title: RNA-Seq of Aradopsis pollen uncovers novel transcription and alternative splicing

Author
item LORAINE, ANN - North Carolina State University
item McCormick, Sheila
item ESTRADA, APRIL - North Carolina State University
item PATEL, K - North Carolina State University
item QIN, PENG - University Of California

Submitted to: Plant Physiology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 4/14/2013
Publication Date: 4/16/2013
Citation: Loraine, A., Mccormick, S.M., Estrada, A., Patel, K., Qin, P. 2013. RNA-Seq of Aradopsis pollen uncovers novel transcription and alternative splicing. Plant Physiology. 162: 1092-1109.

Interpretive Summary: To discover all the genes that are expressed in pollen of the model plant Arabidopsis, a method called RNA-Seq was used; this method also allowed quantification of expression levels. The resulting data were visualized using a web-based tool called Integrated Genome Browser.

Technical Abstract: Pollen grains of Arabidopsis (Arabidopsis thaliana) contain two haploid sperm cells enclosed in a haploid vegetative cell. Upon germination, the vegetative cell extrudes a pollen tube that carries the sperm to an ovule for fertilization. Knowing the identity, relative abundance, and splicing patterns of pollen transcripts will improve our understanding of pollen and allow investigation of tissue-specific splicing in plants. Most Arabidopsis pollen transcriptome studies have used the ATH1 microarray, which does not assay splice variants and lacks specific probe sets for many genes. To investigate the pollen transcriptome, we performed high-throughput sequencing (RNA-Seq) of Arabidopsis pollen and seedlings for comparison. Gene expression was more diverse in seedling, and genes involved in cell wall biogenesis were highly expressed in pollen. RNA-Seq detected at least 4,172 protein-coding genes expressed in pollen, including 289 assayed only by nonspecific probe sets. Additional exons and previously unannotated 5' and 3' untranslated regions for pollen-expressed genes were revealed. We detected regions in the genome not previously annotated as expressed; 14 were tested and 12 were confirmed by polymerase chain reaction. Gapped read alignments revealed 1,908 high-confidence new splicing events supported by 10 or more spliced read alignments. Alternative splicing patterns in pollen and seedling were highly correlated. For most alternatively spliced genes, the ratio of variants in pollen and seedling was similar, except for some encoding proteins involved in RNA splicing. This study highlights the robustness of splicing patterns in plants and the importance of ongoing annotation and visualization of RNA-Seq data using interactive tools such as Integrated Genome Browser.