Nari Kim

Seedling height is an important agronomic trait for early vigor and crop establishment in rice. It is controlled by multiple genes, as shown by the continuous variation and normal distribution observed in the Cheongcheong × Nagdong double haploid population measured from 6 to 24 days after sowing. This study identified 32 quantitative trait loci QTLs associated with seedling height across multiple chromosomes. Subsequent candidate gene analysis within overlapping QTL regions identified 44 genes associated with growth, metabolism, and stress responses. A key finding was the identification of Os06g0282000 on chromosome 6 between RM540 and RM586, which encodes a putative UDP-glucuronosyl/UDP-glucosyltransferase (UGT). This gene showed consistently higher expression in tall CNDH lines and increased expression during the 12-24 DAS period, indicating a positive correlation with seedling growth. Gene Ontology enrichment showed the role of QTL-associated genes in hormone signaling and carbohydrate metabolism, emphasizing their roles in early seedling development. Comparative genomic analysis showed that Os06g0282000 is part of a conserved gene family that includes 51 homologous genes in rice. Phylogenetic analysis supported its close relationship with UGTs involved in regulating plant growth. These findings position Os06g0282000 as a strong candidate gene that may play a key role in seedling height QTLs and emphasize the role of UGT-mediated regulation of phytohormone homeostasis in controlling rice seedling growth and development.

Seed germination and early growth in rice are critical stages influenced by the hormonal balance between gibberellins (GA) and abscisic acid (ABA), particularly under low-temperature stress. This study investigated the effects of GA₃ and ABA on seed germination, embryonic growth, gene expression, and biochemical activities in rice cultivars with contrasting tolerance to low temperatures. GA₃ markedly improved germination in resistant cultivars Nagdong and CNDH77, whereas susceptible cultivars showed minimal improvement, while ABA strongly inhibited germination, especially under higher concentrations. GA₃ also promoted embryonic growth, with resistant cultivars displaying the longest embryo cells (10.10 µm and 13.49 µm, respectively), whereas ABA suppressed embryonic growth and completely inhibited germination in susceptible cultivars. Upregulation of GA biosynthesis (OsCPS1 and OsKS1) and signaling genes (OsGID1 and OsGID2) in resistant cultivars correlated with enhanced germination and growth, whereas ABA-induced ABI5 expression suppressed germination, particularly in susceptible cultivars. Hormone quantification confirmed increased endogenous GA₃ after GA₃ treatment and reduced ABA levels under ABA treatment. Additionally, GA₃ modulated ABA signaling genes, upregulating OSK3, ABI3, ABI4, and ABI5, while ABA treatment had contrasting effects, particularly between resistant and susceptible cultivars. GA₃ treatment also enhanced the expression of GA biosynthesis and signaling genes (OsCPS1, OsKS1, OsGID1, and OsGID2), whereas ABA treatment upregulated ABA catabolic genes (OsABA8ox2). GA₃ also enhanced amylase activity and sugar-related gene expression, supporting its role in energy mobilization during germination. Conversely, ABA suppressed cell elongation, reducing it to 4.45 µm in CNDH77 under 100 µM ABA. These findings provide valuable insights into the hormonal regulation of rice seed germination and growth under low-temperature stress, offering potential strategies to enhance seed vigor and stress tolerance in rice breeding.

Studying hypoxia in rice is particularly important because oxygen deficiency during germination severely limits seedling establishment. Understanding the molecular and physiological mechanisms underlying hypoxic tolerance is therefore crucial for improving rice yield stability under flooded or waterlogged conditions. Progress in developing rice cultivars that thrive under flooding and low oxygen (hypoxic) conditions has been limited over the past two decades due to a lack of tolerant plant varieties and a limited understanding of genetic mechanisms. This study evaluated hypoxia tolerance in the Cheongcheong Nagdong Double Haploid (CNDH) rice population, along with their parent lines, for hypoxia tolerance. Significant phenotypic differences were identified, with the Cheongcheong and CNDH lines CNDH13, CNDH35, and CNDH91 showing strong hypoxia tolerance, while Nagdong and CNDH lines CNDH14-2, CNDH43, and CNDH50-1 were susceptible to hypoxia. Root length was unaffected by hypoxia, while shoot length and fresh weight were key tolerance indicators. Comprehensive quantitative trait loci (QTL) analysis based on logarithm of the odds (LOD) scores above 3.0 identified three QTLs associated with hypoxia tolerance, indicating significant genetic control: qSL-8 and qSL-10 (shoot length) and qFW-2 (fresh weight). The gene expression analysis performed under hypoxic conditions highlighted that 35 candidate genes within these QTL regions exhibited differential regulation: Os02g0184200, Os08g0430200, Os08g0431900, and Os08g0432500 were upregulated, whereas Os08g0439100, Os10g0343400, Os10g0395400, and Os10g0405600 were downregulated in both resistant and susceptible lines. Os08g0431900 displayed significant expression changes correlating with hypoxia resistance. Phylogenetic and protein–protein interaction analyses revealed that Os08g0431900 is highly conserved and interacts with proteins involved in stress responses, suggesting that these proteins are crucial in hypoxia tolerance. These findings provide valuable insights into the genetic basis of hypoxia tolerance and identify key genes for future breeding programs to develop hypoxia-resistant rice varieties.

Progress in developing rice cultivars that thrive under flooding and low oxygen (hypoxic) conditions has been limited over the past two decades due to a lack of tolerant plant varieties and a limited understanding of genetic mechanisms. This study evaluated hypoxia tolerance in the Cheongcheong Nagdong Double Haploid (CNDH) rice population, along with their parent lines, for hypoxia tolerance. Significant phenotypic differences were identified, with the Cheongcheong and CNDH lines CNDH13, CNDH35, and CNDH91 showing strong hypoxia tolerance, while Nagdong and CNDH lines CNDH14-2, CNDH43, and CNDH50-1 were susceptible to hypoxia. Root length was unaffected by hypoxia, while shoot length and fresh weight were key tolerance indicators. Comprehensive quantitative trait loci (QTL) analysis based on logarithm of the odds (LOD) scores above 3.0 identified three QTLs associated with hypoxia tolerance, indicating significant genetic control: qSL-8 and qSL-10 (shoot length) and qFW-2 (fresh weight). The gene expression analysis performed under hypoxic conditions highlighted that 35 candidate genes within these QTL regions exhibited differential regulation: Os02g0184200, Os08g0430200, Os08g0431900, and Os08g0432500 were upregulated, whereas Os08g0439100, Os10g0343400, Os10g0395400, and Os10g0405600 were downregulated in both resistant and susceptible lines. Os08g0431900 displayed significant expression changes correlating with hypoxia resistance. Phylogenetic and protein–protein interaction analyses revealed that Os08g0431900 is highly conserved and interacts with proteins involved in stress responses, suggesting that these proteins are crucial in hypoxia tolerance. These findings provide valuable insights into the genetic basis of hypoxia tolerance and identify key genes for future breeding programs to develop hypoxia-resistant rice varieties.

The number of corn cultivars that have been improved using genetically modified technology continues to increase. However, concerns about the unintentional release of living-modified organisms (LMOs) into the environment still exist. Specifically, there are cases where LMO crops grown as fodder are released into the environment and form a volunteer plant community, which raises concerns about their safety. In this study, we analyzed the possibility of weediness and volunteer plants’ occurrence when GMO fodder corn grains distributed in Korea are unintentionally released into the environment. Volunteer plants’ occurrence was investigated by directly sowing grains in an untreated field. The results showed that the germination rate was extremely low, and even if a corn seed germinated, it could not grow into an adult plant and would die due to weed competition. In addition, the germination rate of edible and fodder grains was affected by temperature (it was high at 20 °C and 30 °C but low at 40 °C and extremely low at 10 °C), and it was higher in the former than in the latter. And the germination rate was higher in Daehakchal (edible corn grains) than in Gwangpyeongok (fodder corn grains). The environmental risk assessment data obtained in this study can be used for future evaluations of the weediness potential of crops and the development of volunteer plant suppression technology in response to unintentional GMO release.

The white-backed planthopper (WBPH) is a major pest of rice crops and causes severe loss of yield. We previously developed the WBPH-resistant rice cultivar “OxF3H” by overexpressing the OsF3H gene. Although there was a higher accumulation of the flavonoids kaempferol (Kr) and quercetin (Qu) as well as salicylic acid (SA) in OxF3H transgenic (OsF3H or Trans) plants compared to the wild type (WT), it is still unclear how OsF3H overexpression affects these WBPH resistant-related changes in gene expression in OxF3H plants. In this study, we analyze RNA-seq data from OxF3H and WT at several points (0 h, 3 h, 12 h, and 24 h) after WBPH infection to explain how overall changes in gene expression happen in these two cultivars. RT-qPCR further validated a number of the genes. Results revealed that the highest number of DEGs (4735) between the two genotypes was detected after 24 h of infection. Interestingly, it was found that several of the DEGs between the WT and OsF3H under control conditions were also differentially expressed in OsF3H in response to WBPH infestation. These results indicate that significant differences in gene expression between the “OxF3H” and “WT” exist as the infection time increases. Many of these DEGs were related to oxidoreductase activity, response to stress, salicylic acid biosynthesis, metabolic process, defense response to pathogen, cellular response to toxic substance, and regulation of hormone levels. Moreover, genes involved in salicylic acid (SA) and ethylene (Et) biosynthesis were upregulated in OxF3H plants, while jasmonic acid (JA), brassinosteroid (Br), and abscisic acid (ABA) signaling pathways were found downregulated in OxF3H plants during WBPH infestation. Interestingly, many DEGs related to pathogenesis, such as OsPR1, OsPR1b, OsNPR1, OsNPR3, and OsNPR5, were found to be significantly upregulated in OxF3H plants. Additionally, genes related to the MAPKs pathway and about 30 WRKY genes involved in different pathways were upregulated in OxF3H plants after WBPH infestation. This suggests that overexpression of the OxF3H gene leads to multiple transcriptomic changes and impacts plant hormones and pathogenic-related and secondary-metabolites-related genes, enhancing the plant’s resistance to WBPH infestation.

Rice (Oryza sativa L.) is one of the essential staple foods for more than half of the world’s population, and its production is affected by different environmental abiotic and biotic stress conditions. The white-backed planthopper (WBPH, Sogatella furcifera) causes significant damage to rice plants, leading to substantial economic losses due to reduced production. In this experiment, we applied exogenous hormones (gibberellic acid and methyl jasmonate) to WBPH-infested rice plants and examined the relative expression of related genes, antioxidant accumulation, the recovery rate of affected plants, endogenous hormones, the accumulation of H₂O₂, and the rate of cell death using DAB and trypan staining, respectively. The expression of the transcriptional regulator (OsGAI) and gibberellic-acid-mediated signaling regulator (OsGID2) was upregulated significantly in GA 50 µM + WBPH after 36 h. OsGAI was upregulated in the control, GA 50 µM + WBPH, GA 100 µM + WBPH, and MeJA 100 µM + WBPH. However, after 48 h, the OsGID2 was significantly highly expressed in all groups of plants. The glutathione (GSH) values were significantly enhanced by GA 100 µM and MeJA 50 µM treatment. Unlike glutathione (GSH), the catalase (CAT) and peroxidase (POD) values were significantly reduced in control + WBPH plants. However, a slight increase in CAT and POD values was observed in GA 50 + WBPH plants and a reduction in the POD value was observed in GA 100 µM + WBPH and MeJA 50 µM + WBPH plants. GA highly recovered the WBPH-affected rice plants, while no recovery was seen in MeJA-treated plants. MeJA was highly accumulated in control + WBPH, MeJA 50 µM + WBPH, and GA 100 µM + WBPH plants. The H₂O₂ accumulation was highly decreased in GA-treated plants, while extensive cell death was observed in MeJA-treated plants compared with GA-treated plants. From this study, we can conclude that the exogenous application of GA can overcome the effects of the WBPH and enhance resistance in rice.

Soil salinity is a major abiotic stress that causes disastrous losses in crop yields. To identify favorable alleles that enhance the salinity resistance of rice (Oryza sativa L.) crops, a set of 120 Cheongcheong Nagdong double haploid (CNDH) lines derived from a cross between the Indica variety Cheongcheong and the Japonica variety Nagdong were used. A total of 23 QTLs for 8 different traits related to salinity resistance on chromosomes 1–3 and 5–12 were identified at the seedling stage. A QTL related to the salt injury score (SIS), qSIS-3b, had an LOD score of six within the interval RM3525–RM15904 on chromosome 3, and a phenotypic variation of 31% was further examined for the candidate genes. Among all the CNDH populations, five resistant lines (CNDH 27, CNDH 34-1, CNDH 64, CNDH 78, and CNDH 112), five susceptible lines (CNDH 52-1, CNDH 67, CNDH 69, CNDH 109, and CNDH 110), and the parent lines Cheongcheong and Nagdong were selected for relative gene expression analysis. Among all the genes, two candidate genes were highly upregulated in resistant lines, including the auxin-responsive protein IAA13 (Os03g0742900) and the calmodulin-like protein 4 (Os03g0743500-1). The calmodulin-like protein 4 (Os03g0743500-1) showed a higher expression in all the resistant lines than in the susceptible lines and a high similarity with other species in sequence alignment and phylogenetic tree, and it also showed a protein–protein interaction with other important proteins. The genes identified in our study will provide new genetic resources for improving salt resistance in rice using molecular breeding strategies in the future.

Low temperature is a serious threat to the seed emergence of rice, which has become one of the main limiting factors affecting rice production in the world. It is of great significance to find the candidate genes controlling low-temperature tolerance during seed germination and study their functions for breeding new rice cultivars with immense low-temperature tolerance during seed germination. In the current experiment, 120 lines of the Cheongcheong Nagdong Double Haploid (CNDH) population were used for quantitative trait locus (QTL) analysis of low-temperature germinability. The results showed a significant difference in germination under low different temperature (LDT) (15 °C, 20 °C) conditions. In total, four QTLs were detected on chromosome 3, 6, and 8. A total of 41 genes were identified from all the four QTLs, among them, 25 genes were selected by gene function annotation and further screened through quantitative real-time polymerase chain reaction (qRT-PCR). Based on gene function annotation and level of expression under low-temperature, our study suggested the OsGPq3 gene as a candidate gene controlling viviparous germination, ABA and GA signaling under low-temperature. This study will provide a theoretical basis for marker-assisted breeding and lay the basis for further mining molecular mechanisms of low-temperature germination tolerance in rice.