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Heading date of rice (Oryza sativa) is a key factor determining rice production and regional adaptability. We analysed the molecular mechanism of OsPIL15, encoding phytochrome-interacting factor-like protein, in delaying rice heading date. Overexpression of OsPIL15 delayed rice heading date by upregulating Hd1 and inhibiting Hd3a and RFT1 expression. OsLF, encoding one rice heading repressor, was found to be the putative candidate regulated by OsPIL15 through a chromatin immunoprecipitation sequencing assay and a transcriptome sequencing assay. OsPIL15 could directly bind to the OsLF promoter and activated its expression. Knocking-out OsLF in OsPIL15-overexpressing lines resulted in flowering 2-3 days earlier, partially rescuing the delayed phenotype. This indicates that overexpression of OsPIL15 overexpression delays heading date partially through OsLF. Protein-protein interaction assay of OsPIL15 or OsPIL15-∆APB (OsPIL15 lacking the active phytochrome B [phyB]-binding [APB] motif) with PHYB showed that the APB motif was required for the interaction between OsPIL15 and PHYB. Furthermore, overexpression of either OsPIL15-∆APB in the wild type or OsPIL15 in the phyB mutant did not delay rice heading date under natural long-day conditions, suggesting that phyB influences OsPIL15-mediated delay in rice heading date.
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http://dx.doi.org/10.1111/pce.15348 | DOI Listing |
Front Plant Sci
August 2025
Rice Science Center, Kasetsart University, Nakhon Pathom, Thailand.
Introduction: Rice is mainly consumed by half of the world's population. The imminent climate change and population growth expected in the next 30 years will outpace the current rice production capacity, posing risks to food and nutrition security in developing nations. One simplified approach to address this challenge is to improve photosynthetic capacity by increasing chlorophyll content in leaves and stems.
View Article and Find Full Text PDFBreed Sci
April 2025
Institute of Crop Science, National Agricultural and Food Research Organization (NARO), Tsukuba, Ibaraki 305-8518, Japan.
Grain chalkiness decreases the appearance quality (APQ) of rice ( L.) grains and reduces consumer satisfaction. Improving APQ is a crucial issue for both marketing and breeding.
View Article and Find Full Text PDFIntroduction: The rice-crab coculture system is ecologically sustainable with efficient resource utilization, but the soil nitrogen cycling mechanisms underlying yield limitations in different coculture models remain unclear. Here, we aimed to identify yield-limiting factors by comparing rice productivity between the conventional rice-crab coculture model (CK) and an optimized model (12 rows cultivated-1 row empty, ERC-12). We hypothesized that ERC-12 enhances crab activity in empty rows, thereby stimulating nifH-mediated soil nitrogen fixation to offset yield losses caused by reduced planting density.
View Article and Find Full Text PDFBMC Plant Biol
August 2025
Jiangsu Key Laboratory of Crop Cultivation and Physiology/ Co-Innovation Center for Modern Production Technology of Grain Crops, Research Institute of Rice Industrial Engineering Technology, Yangzhou University, Yangzhou, 225009, China.
Population characteristics serve as crucial determinants of rice yield. Investigating the population characteristics of indica-japonica hybrid rice across different yield levels can offer a solid theoretical foundation and robust scientific evidence for enhancing high-yield cultivation and breeding efficiency. This study conducted a two-year field experiment on four indica-japonica hybrid rice varieties with three planting densities.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
August 2025
Laboratory of Plant Breeding & Genetics, Department of Agricultural and Environmental biology, The University of Tokyo, Bunkyo-ku 113-8657, Tokyo, Japan.
The () gene integrates red light signals and circadian rhythms to control floral repression under long-day conditions in rice. CRISPR/Cas9 systems were employed to create a series of deletion mutant lines in the upstream regions of , covering a 65-kb genomic region from its transcription start site (TSS). These deletions ranged from 2 to 25 kb in size.
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