Macronuclear Genome Sequence of the Ciliate Tetrahymena thermophila, a Model Eukaryote

Jonathan A. Eisen(J. Craig Venter Institute), Robert S. Coyne(J. Craig Venter Institute), Martin Wu(J. Craig Venter Institute), Dongying Wu(J. Craig Venter Institute), Mathangi Thiagarajan(J. Craig Venter Institute), Jennifer R. Wortman(J. Craig Venter Institute), Jonathan H. Badger(J. Craig Venter Institute), Qinghu Ren(J. Craig Venter Institute), Paolo Amedeo(J. Craig Venter Institute), Kristie M Jones(J. Craig Venter Institute), Luke J. Tallon(J. Craig Venter Institute), Arthur L. Delcher(J. Craig Venter Institute), Steven L. Salzberg(J. Craig Venter Institute), Joana C. Silva(J. Craig Venter Institute), Brian J. Haas(J. Craig Venter Institute), William H. Majoros(J. Craig Venter Institute), Maryam Sharafi Farzad(J. Craig Venter Institute), Jane M. Carlton(J. Craig Venter Institute), Roger K Smith(J. Craig Venter Institute), Jyoti Garg(J. Craig Venter Institute), Ronald E. Pearlman(J. Craig Venter Institute), Kathleen M. Karrer(J. Craig Venter Institute), Lei Sun(J. Craig Venter Institute), Gerard Manning(J. Craig Venter Institute), Nels C. Elde(J. Craig Venter Institute), Aaron P. Turkewitz(J. Craig Venter Institute), David J. Asai(Harvey Mudd College), David E. Wilkes(J. Craig Venter Institute), Yufeng Wang(J. Craig Venter Institute), Hong Cai(The University of Texas at San Antonio), Kathleen Collins(University of California, Berkeley), Balint Stewart(J. Craig Venter Institute), Suzanne R. Lee(J. Craig Venter Institute), Katarzyna Wilamowska(University of Washington), Zasha Weinberg(University of Washington), Walter L. Ruzzo(University of Washington), Dorota Włoga(J. Craig Venter Institute), Jacek Gaertig(J. Craig Venter Institute), Joseph Frankel(J. Craig Venter Institute), Che-Chia Tsao(University of Rochester), Martin A. Gorovsky(University of Rochester), Patrick J. Keeling(University of British Columbia), Ross F. Waller(Canadian Institute for Advanced Research), Nicola J. Patron(J. Craig Venter Institute), J. Michael Cherry(Stanford University), Nicholas A. Stover(Stanford University), C. J. Krieger(J. Craig Venter Institute), Christina del Toro(J. Craig Venter Institute), Hilary F. Ryder(University of California, Santa Barbara), Sondra Williamson(J. Craig Venter Institute), Rebecca Barbeau(University of California, Santa Barbara), Eileen P. Hamilton(J. Craig Venter Institute), Eduardo Orias(University of California, Santa Barbara)
PLoS Biology
August 25, 2006
Cited by 796Open Access
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Abstract

The ciliate Tetrahymena thermophila is a model organism for molecular and cellular biology. Like other ciliates, this species has separate germline and soma functions that are embodied by distinct nuclei within a single cell. The germline-like micronucleus (MIC) has its genome held in reserve for sexual reproduction. The soma-like macronucleus (MAC), which possesses a genome processed from that of the MIC, is the center of gene expression and does not directly contribute DNA to sexual progeny. We report here the shotgun sequencing, assembly, and analysis of the MAC genome of T. thermophila, which is approximately 104 Mb in length and composed of approximately 225 chromosomes. Overall, the gene set is robust, with more than 27,000 predicted protein-coding genes, 15,000 of which have strong matches to genes in other organisms. The functional diversity encoded by these genes is substantial and reflects the complexity of processes required for a free-living, predatory, single-celled organism. This is highlighted by the abundance of lineage-specific duplications of genes with predicted roles in sensing and responding to environmental conditions (e.g., kinases), using diverse resources (e.g., proteases and transporters), and generating structural complexity (e.g., kinesins and dyneins). In contrast to the other lineages of alveolates (apicomplexans and dinoflagellates), no compelling evidence could be found for plastid-derived genes in the genome. UGA, the only T. thermophila stop codon, is used in some genes to encode selenocysteine, thus making this organism the first known with the potential to translate all 64 codons in nuclear genes into amino acids. We present genomic evidence supporting the hypothesis that the excision of DNA from the MIC to generate the MAC specifically targets foreign DNA as a form of genome self-defense. The combination of the genome sequence, the functional diversity encoded therein, and the presence of some pathways missing from other model organisms makes T. thermophila an ideal model for functional genomic studies to address biological, biomedical, and biotechnological questions of fundamental importance.


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