The details are described further in the Supplementary Methods. Sequencing reactions were carried out using universal primer (5′-CTCGGGAAGCGCGCCATTGTGTTGGT-3′) in a capillary DNA sequencer (ABI 3730XL DNA Analyzer, Applied Biosystems). Processed cDNA sequences were used to perform a BLAST search using the GenBank OSI-744 mouse database to compare all available ESTs and genes to the data. BLASTX results with bit scores greater than 80 and e-values less than 10− 10 were regarded as significant. A total of 3840 randomly picked EST clones were sequenced, producing a total of 3251 high-quality ESTs (84.7%) after
removal of clones with no inserts or very short inserts (100 bp cutoff). EST lengths ranged from 100 to 800 bp, selleckchem with a mean of
589 bp. To determine cDNA normalization efficiency and generate a non-redundant EST collection, 3251 high-quality ESTs were submitted to an assembly step to cluster and assemble redundant sequences. 309 contiguous sequences assembled by 764 ESTs and 2487 singleton ESTs were obtained from the finger leather coral cDNA library. Among the 309 contigs, 270 sequences (87.4%) ranged between 500 and 800 bp and 9 (2.9%) were over 1000 bp in length. Most singleton ESTs (1984; 87.4%), ranged between 500 and 700 bp in length. To determine EST identities, the 309 contigs and 2487 singleton ESTs were BLASTx searched against the protein database “nr” which consists all non-redundant GenBank CDS translations, PDB, SwissProt, PIR, PRF excluding
environmental samples from whole genome sequence projects). 1908 (68%) matched a known gene with an E-value < 1e− 10, and the remaining 888 ESTs (32%) did not match any reported gene (Table 1). Although, molecular phylogenetics indicated that coral and the sea anemone diverged approximately 500 million years ago (Stanley and Fautin, 2001), the majority of annotated sequences (814, 42.7%) matched the Sea anemone Nematostella vectensis. It can be reasoned that the Sea anemone is a seemingly primitive animal that, along with corals, jellyfish, and hydras, constitute the oldest eumetazoan phylum, and a draft of the Sea anemone genome sequence has been assembled ( Putnam et al., 2007); however, other corals sequence data have not yet been deposited in public databases Arachidonate 15-lipoxygenase (25 September 2014). Actually, a number of current studies have developed transcriptome datasets for corals (only in scleractinians), including EST collections produced by Sanger sequencing (e.g., Montastrea faveolata, Acropora palmate and Acropora millepora) ( Schwarz et al., 2008) or next-generation sequencing (NGS) (e.g., Acropora mellepora and Pociliopora damicomis) ( Meyer et al., 2009 and Traylor-Knowles et al., 2011). The draft genome of scleractinian coral containing approximately 42 Mb has been decoded from Acropora digitifera using NGS ( Shinzato et al.