The Rice Blast Resistance Gene Pid Family has been Strictly Diverged into Indica and Japonica Subspecies

Background: Rice blast (causative agent the fungus Pyricularia oryzae) represents a major constraint over the productivity of one of the world’s most important staple foods. Genes encoding resistance have been identified in both the indica and japonica subspecies genepools, and combining these within new cultivars represents a rational means of combating the pathogen.Results: In this research, a deeper allele mining was carried out on Pid-2, Pid-3, and Pid-4 by their specific FNP markers in the three panels consisting of 70 indica and 58 japonica cultivars. Within Pid-2, three functional and one non-functional alleles were identified; the former were only identified in indica type entries. At Pid-3, four functional and one non-functional alleles were identified, and once again, all of the former were present in indica type entries. However, the pattern of variation at Pid-4 was rather different: here, the five functional alleles uncovered were dispersed across the japonica type germplasm. Among all the 12 candidate functional alleles, both Pid2-ZS and Pid3-ZS were predominant.Conclusions: Variation in both Pid-2 and Pid-3 appears to have evolved in response to pathogen pressure exerted on indica type cultivars, while that in Pid-4 reflects the interaction between the fungus and the host in japonica type crops. Owning to the founder lineage, ‘Zhenzhuai 11-ZS97’, rather limited genotypes of the Pid family have been effective in both indica and japonica rice groups, of which Pid2-ZS+Pid3-ZS is present in a large proportion of Chinese indica cultivars released since the 1960s.

A Dwarfing Gene sd1-d (Dee-geo-woo-gen dwarf) on Lodging Resistance and Related Traits in Rice

A dwarfing allele at the sd1 locus on chromosome 1 in rice, sd1-d, has been playing important role for developing lodging-resistant and high-yielding indica varieties IR8 and IR36. The dominant allele SD1 for long culm at the locus is differentiated into SD1-in and SD1-ja that are harbored in indica and japonica subspecies, respectively. The sd1-d of IR36 was substituted with SD1-in or SD1-ja by 17 backcrosses with IR36, and two isogenic tall lines were developed by using an indica variety IR5867 and a japonica one ‘Koshihikari’ as donors, which were denoted by “5867-36” and “Koshi-36’’, respectively. The present study was conducted to examine the effect of dwarfing gene sd1-d on lodging resistance and related traits, compared with SD1-in and SD1-ja. Two isogenic lines and IR36 were cultivated in the field of the Faculty of Agriculture and Marine Science, Kochi University, Japan during 2017. Regarding index of lodging (g·cm/g × 100), genotypes were in the order: 5867-36 (97.4) > Koshi-36 (74.1) > IR36 (46.0) on the 21st-day after 80%-heading, and they were in the same order on 10th-day after 80%-heading. The 4th-panicle length (cm) was in the order: 5867-36 (118.7) > Koshi-36 (97.6) > IR36 (78.6). Similarly, the 4th-top weight (g) was in the order: 5867-36 (12.2) > Koshi-36 (10.2) > IR36 (9.6). The highest breaking strength (g) was recorded in IR36 (1649) followed by 5867-36 (1493) whereas the lowest breaking strength (g) was recorded in Koshi-36 (1360). Consequently, it is inferred that sd1-d enhances lodging resistance due to the decreases in the length and weight above the 4th-internode as well as the increase of breaking strength. The effect of SD1-in on lodging resistance is lower than that of SD1-ja.

Characterization of the Common Japonica-Originated Genomic Regions in the High-Yielding Varieties Developed from Inter-Subspecific Crosses in Temperate Rice (Oryza sativa L.)

The inter-subspecific crossing between indica and japonica subspecies in rice have been utilized to improve the yield potential of temperate rice. In this study, a comparative study of the genomic regions in the eight high-yielding varieties (HYVs) was conducted with those of the four non-HYVs. The Next-Generation Sequencing (NGS) mapping on the Nipponbare reference genome identified a total of 14 common genomic regions of japonica-originated alleles. Interestingly, the HYVs shared japonica-originated genomic regions on nine chromosomes, although they were developed through different breeding programs. A panel of 94 varieties was classified into four varietal groups with 38 single nucleotide polymorphism (SNP) markers from 38 genes residing in the japonica-originated genomic regions and 16 additional trait-specific SNPs. As expected, the japonica-originated genomic regions were only present in the japonica (JAP) and HYV groups, except for Chr4-1 and Chr4-2. The Wx gene, located within Chr6-1, was present in the HYV and JAP variety groups, while the yield-related genes were conserved as indica alleles in HYVs. The japonica-originated genomic regions and alleles shared by HYVs can be employed in molecular breeding programs to further develop the HYVs in temperate rice.

Characterization of the Common japonica-Originated Genomic Regions in the High Yielding Varieties Developed from Inter-Subspecific Crosses in Rice (Oryza sativa L.)

The inter-subspecific crossing between indica and japonica subspecies in rice have been utilized to improve yield potential in temperate rice. In this study, a comparative study of the genomic regions in the eight high yielding varieties (HYVs) was conducted with those of the four non-HYV varieties. NGS mapping on the Nipponbare reference genome identified a total of 14 common genomic regions of japonica-originated alleles. Interestingly, the HYVs shared the japonica-originated genomic regions on the nine chromosomes, although they were developed from different breeding programs. A panel of 94 varieties was classified into four varietal groups with the 39 SNP markers from 39 genes residing the japonica-originated genomic regions and 16 additional trait-specific SNPs. As expected, the japonica originated genomic regions were present only in JAP and HYV groups with exceptions for Chr4-1 and Chr4-2. The Wx gene located within Chr6-1 was present in HYV and JAP variety groups, while the yield-related genes were conserved as indica alleles in HYVs. The japonica-originated genomic regions and alleles shared by HYVs can be employed in molecular breeding programs for further development of HYVs in rice.

Correlation of biological, biochemical and technological quality traits of germplasm of the rice collection

Collection of Oryza sativa L. total more than 7.0 thousand samples was formed in the All-Russian Rice Research Institute. Based on the complex of biological, biochemical and technological traits, a comparative evaluation of 112 rice samples of Indica and Japonica subspecies from remote regions of world rice growing in the conditions of southern Russia was carried out. The paired correlations between the traits are determined. Genotypic variation of amylose content was in the range of 16.8 - 31.4%, protein - 7.2 - 11.2%. Promising genotypes that combine high levels of protein and amylose for quality breeding have been identified.

Characterization of Indonesian pigmented rice (Oryza sativa) based on morphology and Single Nucleotide Polymorphisms

Kurniasih NS, Susandarini R, Susanto FA, Nuringtyas TR, Jenkins G, Purwestri YA. 2019. Characterization of Indonesian pigmented rice (Oryza sativa) based on morphology and Single Nucleotide Polymorphisms. Biodiversitas 20: 1208-1214. Indonesia has many cultivars of pigmented rice, but many variants have not been characterized using morphological characters and molecular markers. SNPs (Single Nucleotide polymorphisms) have been used in previous studies to identify the Indica and Japonica subspecies. Characterization of whether a line belongs to the Indica or Japonica subspecies is useful information for rice breeders, especially to generate line exhibiting the strong hybrid vigor. Morphological characters are used to determine the relationship between cultivars using cluster analysis. The SNP markers were amplified by PCR, sequenced and compared with sequences in the GenBank. Based on morphological characters, ten cultivars divide into two clusters. SNPs distinguish Indica and Japonica subspecies, and show that Hitam Lampung, Aek Sibundong, Melik, Hitam Toraja, Merah Kalimantan, and Merah Sumbawa belong to the Indica subspecies while Cempo Ireng and Pare Eja belong to Japonica. Abang Segreng and Hitam Toraja could not be clearly assigned to either the Indica or Japonica subspecies.