![]() ![]() In teleost fish, genome annotation is further seriously hindered by genome duplication. To obtain information about the portion of a genome that is transcribed as RNAs and then translated into proteins, a comprehensive set of full-length transcripts is needed. It is still problematic at present to predict the correct distribution of CDS regions solely based on genomic sequences. In eukaryotes, prediction of CDS regions in genomic sequence is complicated by the intron interruptions and the low proportion of protein coding regions in the genome. An important step in genome analysis is to decipher the complete protein coding sequence (CDS) region of each gene. However, thorough genome analysis thereafter is essential to associate genome sequences with biological meanings. Such efforts have produced a wealth of genome resources. Recent advances in next-generation sequencing enabled an array of whole genome sequencing or re-sequencing projects in both model and non-model species. The putative set of duplicated genes provide a starting point for genome scale analysis of gene duplication in the catfish genome, and should be a valuable resource for comparative genome analysis, genome evolution, and genome function studies. The large set of transcripts assembled in this study is the most comprehensive set of genome resources ever developed from catfish, which will provide the much needed resources for functional genome research in catfish, serving as a reference transcriptome for genome annotation, analysis of gene duplication, gene family structures, and digital gene expression analysis. The characterization of consensus sequences surrounding start codon and the stop codon confirmed the correct assembly of the full-length transcripts. Of the 25,144 contigs with unique protein hits, around 20,000 contigs matched 50% length of reference proteins, and over 14,000 transcripts were identified as full-length with complete open reading frames. A total of 2,659 unique genes were identified as putative duplicated genes in the catfish genome because the assembly of the corresponding transcripts harbored PSVs or MSVs (in the form of pseudo-SNPs in the assembly). Functional annotation of the assembly allowed identification of 25,144 unique protein-encoding genes. Assembly of these reads generated 370,798 non-redundant transcript-derived contigs. Deep sequencing of the doubled haploid channel catfish transcriptome was performed using Illumina HiSeq 2000 platform, yielding over 300 million high-quality trimmed reads totaling 27 Gbp. As such, transcript sequences generated from next-generation sequencing can be favorably assembled into full-length transcripts. In this work, we took advantage of a doubled haploid catfish, which has two sets of identical chromosomes and in theory there should be no allelic variations. Generation of large numbers of full-length transcripts using traditional transcript sequencing is very difficult and extremely costly. To conduct phylogenetic analysis and orthology analysis, full-length transcripts are essential. Rather intense phylogenetic analysis or structural analysis of orthologies is required for the identification of genes. Because of gene duplications, one cannot establish orthologies simply by homology comparisons. In teleost fish, genome annotation is seriously hindered by genome duplication. Genome annotation depends on the availability of transcript information as well as orthology information. Upon the completion of whole genome sequencing, thorough genome annotation that associates genome sequences with biological meanings is essential. ![]()
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