The Sanger Institute has sequenced the genome of the Eimeria tenella Houghton strain to 7x coverage using capillary sequencing. In addition, both Illumina and 454 sequencing technologies have been used to improve the assembly. Transcriptome sequencing (mRNA-seq) is being used to improve the annotation of the genome and also to examine changes in gene expression between different life stages.
The Eimeria tenella genome project at The Sanger Institute, a joint collaboration with Drs. Martin Shirley and Fiona Tomley (Institute of Animal Health, Compton, UK), has been funded by the BBSRC.
Published Genome Data
The Houghton strain of Eimeria tenella was selected by the research community for the genome project. The genome is approximately 60 MB in size, with a GC content of approximately 53%. There are 14 chromosomes that range in size from 1Mb to > 6Mb. Two major ribosomal DNA clusters, that account for some 2.5% of the genome size, have been mapped as tandem arrays on chromosome 12 (140 copies of an 8 Kb 18S-5.8S-28S unit) and chromosome 10 (500 copies of a 730bp 5S unit).
RNA-Seq of E. tenella Houghton life cycle stages
Sample | Strain | Run Accession |
|---|---|---|
| sporozoite_RNA | Houghton | ERR178634 |
| 2ndgenmerozoites_v_2 | Houghton | ERR178635 |
| sporulatedoocyst_v_2 | Houghton | ERR178636 |
| unsporulatedoocyst_v_2 | Houghton | ERR178637 |
| v4unsporulateoocyst | Houghton | ERR178638 |
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Sequencing and analysis of chromosome 1 of Eimeria tenella reveals a unique segmental organization.
Genome research 2007;17;3;311-9
PUBMED: 17284678; PMC: 1800922; DOI: 10.1101/gr.5823007


