Research
Improved genome assembly and evidence-based global gene model set for the chordate Ciona intestinalis: new insight into intron and operon populations
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* Corresponding author: Yutaka Satou yutaka@ascidian.zool.kyoto-u.ac.jp
1 Department of Zoology, Graduate School of Science, Kyoto University, Sakyo, Kyoto, 606-8502, Japan
2 Graduate School of Information Science and Technology, Hokkaido University, N14W9, Sapporo, 060-0814, Japan
3 Graduate School of Science and Technology, Chiba University, Inage, Chiba, 263-8522, Japan
4 Shimoda Marine Research Center, University of Tsukuba, Shimoda, Shizuoka, 415-0025, Japan
5 Division of Disease Proteomics, Institute for Enzyme Research, The University of Tokushima, 3-15-18 Kuramoto-cho, Tokushima, 770-8503, Japan
6 Montreal Neurological Institute and Departments of Neurology and Neurosurgery and Biology, McGill University, 3801 University St, Montreal, Quebec, H3A 2B4, Canada
7 McGill University and Genome Quebec Innovation Centre, and Department of Human Genetics, McGill University, Montreal, Quebec, H3A 2B4, Canada
8 Advanced Center for Genome Technology, and Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, 73019-0370, USA
9 Department of Biology, San Diego State University, San Diego, California, 92182-4614, USA
10 Institut de Biologie du Developpement de Marseille Luminy (IBDML), CNRS-UMR6216/Universite de la Mediterranee Aix-Marseille, Marseille, 13288, France
11 DOE Joint Genome Institute, Genomic Technologies Department, 2800 Mitchell Drive, Walnut Creek, California, 94598, USA
12 Faculty of Science and Technology, Keio University, Kouhoku, Yokohama, 223-8522, Japan
Genome Biology 2008, 9:R152 doi:10.1186/gb-2008-9-10-r152
Published: 14 October 2008Abstract
Background
The draft genome sequence of the ascidian Ciona intestinalis, along with associated gene models, has been a valuable research resource. However, recently accumulated expressed sequence tag (EST)/cDNA data have revealed numerous inconsistencies with the gene models due in part to intrinsic limitations in gene prediction programs and in part to the fragmented nature of the assembly.
Results
We have prepared a less-fragmented assembly on the basis of scaffold-joining guided by paired-end EST and bacterial artificial chromosome (BAC) sequences, and BAC chromosomal in situ hybridization data. The new assembly (115.2 Mb) is similar in length to the initial assembly (116.7 Mb) but contains 1,272 (approximately 50%) fewer scaffolds. The largest scaffold in the new assembly incorporates 95 initial-assembly scaffolds. In conjunction with the new assembly, we have prepared a greatly improved global gene model set strictly correlated with the extensive currently available EST data. The total gene number (15,254) is similar to that of the initial set (15,582), but the new set includes 3,330 models at genomic sites where none were present in the initial set, and 1,779 models that represent fusions of multiple previously incomplete models. In approximately half, 5'-ends were precisely mapped using 5'-full-length ESTs, an important refinement even in otherwise unchanged models.
Conclusion
Using these new resources, we identify a population of non-canonical (non-GT-AG) introns and also find that approximately 20% of Ciona genes reside in operons and that operons contain a high proportion of single-exon genes. Thus, the present dataset provides an opportunity to analyze the Ciona genome much more precisely than ever.