De novo assembly and characterization of the garlic (Allium sativum) bud transcriptome by Illumina sequencing.
Plant Cell Rep, 2012/10;31(10):1823-8.
Sun X[1], Zhou S, Meng F, Liu S
Affiliations
PMID: 22684307DOI: 10.1007/s00299-012-1295-z
Impact factor: 4.964
Abstract
Garlic is widely used as a spice throughout the world for the culinary value of its flavor and aroma, which are created by the chemical transformation of a series of organic sulfur compounds. To analyze the transcriptome of Allium sativum and discover the genes involved in sulfur metabolism, cDNAs derived from the total RNA of Allium sativum buds were analyzed by Illumina sequencing. Approximately 26.67 million 90 bp paired-end clean reads were achieved in two libraries. A total of 127,933 unigenes were generated by de novo assembly and were compared with the sequences in public databases. Of these, 45,286 unigenes had significant hits to the sequences in the Nr database, 29,514 showed significant similarity to known proteins in the Swiss-Prot database and, 20,706 and 21,952 unigenes had significant similarity to existing sequences in the KEGG and COG databases, respectively. Moreover, genes involved in organic sulfur biosynthesis were identified. These unigenes data will provide the foundation for research on gene expression, genomics and functional genomics in Allium sativum. Key message The obtained unigenes will provide the foundation for research on functional genomics in Allium sativum and its closely related species, and fill the gap of the existing plant EST database.
MeSH terms
Algorithms; Computational Biology; Databases, Genetic; Expressed Sequence Tags; Garlic; Gene Expression Profiling; Genes, Plant; Genomic Library; Genomics; Plant Proteins; RNA, Plant; Software; Sulfur; Transcriptome
More resources
EndNote: Download