Ji-Hyun Kim, Ye-Jin Son, Eui-Jung Kim, Ki-Hong Jung, Yu-Jin Kim
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引用次数: 0
Abstract
Pollen tubes are crucial for angiosperm plants, as they deliver sperm gametes for the essential process of double fertilization. Understanding the molecular mechanisms behind pollen tube germination and growth is critical; however, these processes remain partially elucidated in monocot cereal crops. Rapid Alkalinization Factor (RALF), a small peptide of about 5 kDa, binds to the CrRLK1L receptor and plays a role in various plant physiological processes, including reproduction and tip growth. Recently, we reported that OsRALF17 and OsRALF19 binds to the OsMTD2, pollen specific CrRLK1L member, and regulates pollen tube growth. In this study, we demonstrate that Ruptured Pollen tube (RUPO), another CrRLK1L member, is also a putative receptor for OsRALF17 and OsRALF19, and propose the formation of a receptor complex with OsMTD2. In tobacco epidermal cells, OsMTD2 and RUPO were co-localized at both the plasma membrane (PM) and the nuclear membrane. Additionally, we generated a RUPO-tagged line driven by its native promoter to visualize subcellular localization during pollen tube growth. RUPO localizes a tip-enriched distribution, with intense fluorescence at the tip's PM and cytoplasm in pollen tube. Upon treatment with synthetic OsRALF17M and OsRALF19M peptides, a reduction in the signal near the PM was observed, suggesting a potential response to these peptides. Our data support the role of RUPO as a candidate receptor for OsRALF17 and OsRALF19 in rice pollen tubes, thereby suggesting a novel mechanism for these RALFs in regulating pollen tube function. Additionally, we observed a significant delay in pollen tube burst time upon treatment with synthetic OsRALF17M and synthetic OsRALF19M. We propose that investigating this phenomenon may provide further insights into the specific signaling pathways mediated by these RALFs.
期刊介绍:
The Journal of Plant Physiology is a broad-spectrum journal that welcomes high-quality submissions in all major areas of plant physiology, including plant biochemistry, functional biotechnology, computational and synthetic plant biology, growth and development, photosynthesis and respiration, transport and translocation, plant-microbe interactions, biotic and abiotic stress. Studies are welcome at all levels of integration ranging from molecules and cells to organisms and their environments and are expected to use state-of-the-art methodologies. Pure gene expression studies are not within the focus of our journal. To be considered for publication, papers must significantly contribute to the mechanistic understanding of physiological processes, and not be merely descriptive, or confirmatory of previous results. We encourage the submission of papers that explore the physiology of non-model as well as accepted model species and those that bridge basic and applied research. For instance, studies on agricultural plants that show new physiological mechanisms to improve agricultural efficiency are welcome. Studies performed under uncontrolled situations (e.g. field conditions) not providing mechanistic insight will not be considered for publication.
The Journal of Plant Physiology publishes several types of articles: Original Research Articles, Reviews, Perspectives Articles, and Short Communications. Reviews and Perspectives will be solicited by the Editors; unsolicited reviews are also welcome but only from authors with a strong track record in the field of the review. Original research papers comprise the majority of published contributions.