Sister project / Reference
Phytozome
Comparative genomics of land plant proteomes, from the same team and framework as Metazome. This reference record preserves the Phytozome page distributed with Metazome release 2.0.4.
Overview
Phytozome is a joint project of the U.S. Department of Energy's Joint Genome Institute and the University of California to facilitate comparative genomic studies among land plants. Clusters of orthologous and paralogous genes that represent the modern descendants of ancestral gene sets are constructed at key phylogenetic nodes. These clusters allow easy access to clade specific orthology and paralogy relationships as well as clade specific genes and gene expansions.
As of version 2.0.4, Phytozome provides access to six sequenced and annotated land plant genomes, five of which have been clustered into gene families at six evolutionarily significant nodes. Where possible, each gene has been annotated with PFAM, KOG, KEGG, and PANTHER assignments, and publicly available annotations from RefSeq, UniProt, TAIR, and JGI are hyperlinked and searchable.
Included organisms
The proteomes of the following organisms are clustered in release 2.0.4 of Phytozome. Several organism names link to the current Phytozome record for that species.
| Organism | Common name | Source |
|---|---|---|
| Arabidopsis thaliana | Mouse ear cress | Release 6 annotation |
| Oryza sativa | Rice | As distributed with Phytozome 2.0.4 |
| Populus trichocarpa | Poplar | Annotation of the v1.0 assembly |
| Sorghum bicolor | Sweet sorghum | Preliminary Genomescan annotation of assembly sbi0 |
| Physcomitrella patens | Moss | As distributed with Phytozome 2.0.4 |
Access is also provided to the sequence and annotation of soybean, though it is not yet included in Phytozome gene families.
| Organism | Common name | Source |
|---|---|---|
| Glycine max | Soybean | Preliminary Genomescan, FgenesH, and PASA annotation Glyma0.1 of assembly Glyma0 |
Nodes
Clustering is used to group extant genes into sets representing the ancestral genes that existed just prior to various significant evolutionary events, called nodes. Extant genes have been clustered at nodes representing the following speciation and genome wide duplication events.
- Land Plants node, about 450 Mya
- Genes representing the most recent common ancestor of Tracheophyta, represented by angiosperms, and bryophyta, represented by the moss Physcomitrella.
- Angiosperms node, about 120 Mya
- Genes representing the most recent common ancestor of grasses (Sorghum and Rice) and Rosids (Arabidopsis and Poplar).
- Grasses, about 68 Mya
- Genes representing the most recent common ancestor of Sorghum and Rice.
- Rosids, about 110 Mya
- Genes representing the most recent common ancestor of Arabidopsis and Poplar.
- Poplar duplication, about 60 Mya
- Genes representing the ancestral gene set just prior to the post speciation genome wide duplication in poplar.
- Arabidopsis duplication, about 60 Mya
- Genes representing the ancestral gene set just prior to the post speciation genome wide duplication in Arabidopsis.
Clustering methodology
Clustering is performed hierarchically, from the crown nodes to the root. First, the recent whole genome duplications in poplar and Arabidopsis were analyzed. Next, poplar and Arabidopsis (Rosid) clusters were created as described above from poplar and Arabidopsis orthologs, while requiring that all previous intraspecies clusters remain together.
The Grass node captures the rice and sorghum common ancestor. The Angiosperm node, covering poplar, Arabidopsis, rice, and sorghum, was created from grass and Rosid orthologs, requiring all previous Rosid and grass clusters to remain together. The final land plant node was created using mutual best hits between the spike moss Physcomitrella patens and previously clustered plants as orthologs, as there is not a detectable syntenic signal left at this scale of evolutionary time.
By construction, every gene from an organism present at a particular node is in one and only one cluster at that node. Some clusters may contain only one extant gene, called a singleton. Singletons can come from fast evolution leading to so much sequence divergence that sequence similarity based clustering is confounded, from gene loss, or from gene calling errors.
Clustering statistics
| Node | Gene families | Singletons | Median family size | Largest family |
|---|---|---|---|---|
| Land Plants | 10,232 | 14,117 | 6 | 499, No apical meristem (NAM) protein |
| Angiosperms | 11,963 | 13,467 | 5 | 410, F box domain and leucine rich repeat |
| Grasses | 15,362 | 7,562 | 2 | 362, retrotransposon |
| Rosids | 13,976 | 6,785 | 3 | 112, Plant protein of unknown function |
| Poplar Duplication | 9,564 | 24,679 | 2 | 15, Leucine rich repeat |
| Arabidopsis Duplication | 2,686 | 20,095 | 2 | 25, Tyrosine Kinase |
Phytozome team
| Role | Contributors |
|---|---|
| Software | David M. Goodstein, Rusty Howson, Rochak Neupane, Shengqiang Shu |
| Analysis | Bill Dirks, Uffe Hellsten, Therese Mitros, Dan Rokhsar |