IC4R002-Genome-2002-11935018

Project Title

• A Draft Sequence of the Rice Genome (Oryza sativa L. ssp.japonica)

The Background of This Project

• The genome of the japonica subspecies of rice, an important cereal and model monocot, was sequenced and assembled by whole-genome shotgun sequencing. The assembled sequence covers 93% of the 420-megabase genome. Gene predictions on the assembled sequence suggest that the genome contains 32,000 to 50,000 genes. Homologs of 98% of the known maize, wheat, and barley proteins are found in rice. Synteny and gene homology between rice and the other cereal genomes are extensive, whereas synteny with Arabidopsis is limited. Assignment of candidate rice orthologs to Arabidopsis genes is possible in many cases. The rice genome sequence provides a foundation for the improvement of cereals, our most important crops.

Research Findings

• Translated HMLgenes300 were classified with the software package INTERPRO (27,28). INTERPRO output was filtered to create sets of the longest protein domain for each associated protein, and domains were categorized using Gene Ontology (GO) software(29). The results of these classifications are shown in Fig. 1; about 44% of Hgenes, 32% of Mgenes, and 5% of Lgenes were classified, respectively. Most of the classified proteins fall into the categories of metabolism and cell communication/signal transduction.

Fig. 1. Rice gene prediction classifications. HMLgenes300 were classified with Interpro and GO software (27–29); the categories generated are shown.

• Eighty-five percent of Arabidopsis predicted proteins (21,590 of 25,554) were significantly homologous to HMLgenes300 predicted proteins; of these, 2565 show very strong conservation between Arabidopsis and rice (Fig. 2).

Fig. 2. Similarity of 25,554 Arabidopsis proteins and best rice homologs. Predicted Arabidopsis proteins (October 2001, ftp.tigr.org) were compared (BLASTP E value # –6) with HMLgenes300 translations.The expectation values range from E , 2180(high homology) to E . 26 (low homology) and are depicted in intervals spanning 10 exponents(e.g., , 2180, 2180 to 2171, 2170 to 2161, etc.)

• Flowering in Arabidopsis is initiated by flowering-time genes that activate floral meristem identity genes, leading to the patterned expression of floral organ identity genes (Fig. 3). Rice contains single-copy homologs of the Arabidopsis flowering-time genes GI, CO, LD, and FCA.

Fig. 3. Flowering-time and flower development genes in the rice genome. A simplified model shows the predicted genetic network regulating flowering time and flower development in Arabidopsis, with gene names color-coded to indicate clearidentification of an ortholog in the rice genome (red) or no clear identification(white). In Arabidopsis there are three genetic pathways that control flowering time (100, 101). The long-day pathway represented by GI and CO and the autonomous pathway represented by LD, FCA, and FLC are likely integrated through FT and AGL20 to promote activation of meristem identity genes LFY, AP1, and CAL.The vernalization pathway, represented by FRI, feeds into the autonomous pathway upstream of FLC. The GA pathway,represented by GA1, leads to the activation of LFY. TFL serves to restrict the expression of the meristem identity genes to floral meristems, where they promote the patterned expression of floral organ identity genes AP2, AP3, PI, and AG, which are also affected by the regulatory genes ANT, UFO, and SUP (102, 103).

Fig. 4. Rice-maize synteny. Maize markers were mapped to the rice genome in silico. Maize map and sequence information were derived from MaizeDB (610 markers) and GenBank, respectively. Maize chromosomes are indicated along the vertical black lines; positions of specific markers and bins are defined by horizontal lines. Rice chromosomes are represented by numbered, colored rectangles. Significant homology (at least 80% identity, over 100 continuous base pairs, between a maize chromosomal region and a particular rice region) is indicated by a colored rectangle to the right of the maize chromosome. For a more detailed version of this map, see Web site link 24.

Labs working on this Project

• Torrey Mesa Research Institute, Syngenta, 3115 Merryfield Row, San Diego, CA 92121, USA (www.tmri.org).
• Bryan College, Dayton, TN 37321, USA.
• Department of Biological Sciences, Northern Illinois University, DeKalb, IL 60115, USA.
• Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720, USA.
• Clemson University Genomics Institute, 100 Jordan Hall, Clemson, SC 29630, USA.
• Myriad Genetics, 320 Wakara Way, Salt Lake City,UT 84108, USA.

Corresponding Author

• stephen.goff@syngenta.com