The zebrafish reference genome sequence and its relationship to the human genome
Последовательность референсного генома данио-рерио и ее взаимосвязь с геномом человека
2013-04-16
SCID: 54.1/uqpxswry
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chemical mutagenesisgenome sequence assemblyhuman-zebrafish orthologyprotein-coding geneszebrafish reference genome
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Abstract (AI)
A high-quality sequence assembly of the zebrafish genome reveals the largest gene set of any vertebrate and provides information on key genomic features, and comparison to the human reference genome shows that approximately 70% of human protein-coding genes have at least one clear zebrafish orthologue. The genome of the zebrafish — a key model organism for the study of development and human disease — has now been sequenced and published as a well-annotated reference genome. Zebrafish turns out to have the largest gene set of any vertebrate so far sequenced, and few pseudogenes. Importantly for disease studies, comparison between human and zebrafish sequences reveals that 70% of human genes have at least one obvious zebrafish orthologue. A second paper reports on an ongoing effort to identify and phenotype disruptive mutations in every zebrafish protein-coding gene. Using the reference genome sequence along with high-throughput sequencing and efficient chemical mutagenesis, the project's initial results — covering 38% of all known protein-coding genes — they describe phenotypic consequences of more than 1,000 alleles. The long-term goal is the creation of a knockout allele in every protein-coding gene in the zebrafish genome. All mutant alleles and data are freely available at go.nature.com/en6mos . Zebrafish have become a popular organism for the study of vertebrate gene function1,2. The virtually transparent embryos of this species, and the ability to accelerate genetic studies by gene knockdown or overexpression, have led to the widespread use of zebrafish in the detailed investigation of vertebrate gene function and increasingly, the study of human genetic disease3,4,5. However, for effective modelling of human genetic disease it is important to understand the extent to which zebrafish genes and gene structures are related to orthologous human genes. To examine this, we generated a high-quality sequence assembly of the zebrafish genome, made up of an overlapping set of completely sequenced large-insert clones that were ordered and oriented using a high-resolution high-density meiotic map. Detailed automatic and manual annotation provides evidence of more than 26,000 protein-coding genes6, the largest gene set of any vertebrate so far sequenced. Comparison to the human reference genome shows that approximately 70% of human genes have at least one obvious zebrafish orthologue. In addition, the high quality of this genome assembly provides a clearer understanding of key genomic features such as a unique repeat content, a scarcity of pseudogenes, an enrichment of zebrafish-specific genes on chromosome 4 and chromosomal regions that influence sex determination.
Key Findings
1
A complementary mutagenesis project initially surveyed 38% of known zebrafish protein-coding genes and characterized phenotypic consequences of more than 1,000 alleles.
2
A high-quality, well-annotated zebrafish reference genome assembly identifies the largest gene set reported among vertebrates sequenced to date.
3
Approximately 70% of human protein-coding genes have at least one clear zebrafish orthologue, supporting zebrafish as a model for human disease studies.
4
The project aims to generate knockout alleles for every zebrafish protein-coding gene, with mutant alleles and associated data made freely available.
5
The zebrafish genome contains relatively few pseudogenes despite its large gene set.
Research Object
the zebrafish reference genome and its orthologous relationship to the human genome
Research Subject
genome organization, gene-set composition, and conservation of protein-coding genes between zebrafish and humans
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2013-04-16
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