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Protoplasma ; 248(4): 651-62, 2011 Oct.
Article in English | MEDLINE | ID: mdl-20978809

ABSTRACT

The degeneration of three of four meiotic products is a very common process in the female gender of oogamous eukaryotes. In Tillandsia (and many other angiosperms), the surviving megaspore has a callose-free wall in chalazal position while the other three megaspores are completely embedded in callose. Therefore, nutrients and signals can reach more easily the functional megaspore from the nucellus through the chalazal pole with respect to the other megaspores. The abortion of three of four megaspores was already recognized as the result of a programmed cell death (PCD) process. We investigated the process to understand the modality of this specific type of PCD and its relationship to the asymmetric callose deposition around the tetrad. The decision on which of the four megaspores will be the supernumerary megaspores in angiosperms, and hence destined to undergo programmed cell death, appears to be linked to the callose layer deposition around the tetrad. During supernumerary megaspores degeneration, events leading to the deletion of the cells do not appear to belong to a single type of cell death. The first morphological signs are typical of autophagy, including the formation of autophagosomes. The TUNEL positivity and a change in morphology of mitochondria and chloroplasts indicate the passage to an apoptotic-like PCD phase, while the cellular remnants undergo a final process resembling at least partially (ER swelling) necrotic morphological syndromes, eventually leading to a mainly lipidic cell corpse still separated from the functional megaspore by a callose layer.


Subject(s)
Apoptosis , Bromeliaceae/physiology , Gametogenesis, Plant , Glucans/physiology , Ovule/cytology , Bromeliaceae/cytology , Bromeliaceae/genetics , Bromeliaceae/growth & development , Cell Nucleus/genetics , Cell Nucleus/physiology , Cell Nucleus/ultrastructure , Chloroplasts/physiology , DNA Fragmentation , DNA, Plant/analysis , Endoplasmic Reticulum/physiology , Endoplasmic Reticulum/ultrastructure , In Situ Nick-End Labeling , Meiosis , Microscopy, Electron, Transmission , Microscopy, Fluorescence , Mitochondria/physiology , Ovule/genetics , Ovule/physiology , Ovule/ultrastructure , Vacuoles/physiology , Vacuoles/ultrastructure
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