Calcium is widely known to have a role as a signaling molecule in many different processes, including stress response and activation of the embryogenic program. However, there are no direct clues about calcium levels during microspore embryogenesis, an experimental process that combines a developmental switch toward embryogenesis and the simultaneous application of different stressing factors. In this work, we used FluoForte, a calcium-specific fluorescent vital dye, to track by confocal microscopy the changes in levels and subcellular distribution of calcium in living rapeseed ( and eggplant microspores and pollen grains during development, as well as during the first stages of -induced microspore embryogenesis in rapeseed. During development, a clear peak of cytosolic Ca was observed in rapeseed vacuolate microspores and young pollen grains, the stages more suitable for embryogenesis induction. However, the Ca levels observed in eggplant were dramatically lower than in rapeseed. Just after induction, Ca levels increased specifically in rapeseed embryogenic microspores at levels dramatically higher than during development. The increase was observed in the cytosol, but predominantly in vacuoles. Non-embryogenic forms such as callus-like and pollen-like structures presented remarkably different calcium patterns. After the heat shock-based inductive treatment, Ca levels progressively decreased in all cases. Together, our results reveal unique calcium dynamics in rapeseed microspores, as well as in those reprogrammed to embryogenesis, establishing a link between changes in Ca level and subcellular distribution, and microspore embryogenesis.
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http://dx.doi.org/10.3389/fpls.2017.01177 | DOI Listing |
Protoplasma
January 2025
College of Horticulture, Shenyang Agricultural University, Shenhe District, 120 Dongling Road, Shenyang, China.
Microspore culture is an efficient and rapid method that produces doubled haploid (DH) lines for hybrid breeding in crops and vegetables. However, the low frequency of microspore embryogenesis and spontaneous diploidization in Chinese kale still require improvement. In the present work, an efficient microspore culture protocol was constructed and used for DH producing in Chinese kale breeding.
View Article and Find Full Text PDFPlant Sci
February 2025
Pollen Biotechnology of Crop Plants Group, Margarita Salas Center of Biological Research, CIB-CSIC, Ramiro de Maeztu 9, Madrid 28040, Spain. Electronic address:
In vivo, microspores in the anthers follow the gametophytic development pathway, culminating in the formation of pollen grains. Conversely, in vitro, under stress treatments, microspores can be reprogrammed into totipotent cells, initiating an embryogenic pathway that produces haploid and double-haploid embryos, which are important biotechnological tools in plant breeding. There is growing evidence that epigenetic reprogramming occurs during microspore embryogenesis through DNA methylation, but less is known about the role of histone modifications.
View Article and Find Full Text PDFFront Plant Sci
November 2024
Pollen Biotechnology of Crop Plants Group, Biological Research Center (CIB) - Spanish National Research Council (CSIC), Madrid, Spain.
Plants (Basel)
October 2024
Department of Herbal Crop Research, NIHHS, RDA, Eumseong 27709, Republic of Korea.
Anther and microspore cultures are efficient methods for inducing haploids in plants. The microspore culture by chromosome-doubling method can produce double haploid lines, developing pure lines within the first or second generations. This study aimed to induce haploid plants in using the shed-microspore culture method.
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