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Calreticulin expression in relation to exchangeable Ca(2+) level that changes dynamically during anthesis, progamic phase, and double fertilization in Petunia
by
Lenartowski, Robert
, Suwińska, Anna
, Lenartowska, Marta
in
Blotting, Western
/ Calcium - metabolism
/ Calreticulin - metabolism
/ Calreticulin - ultrastructure
/ Fertilization
/ Flowers - metabolism
/ Flowers - ultrastructure
/ Kinetics
/ Microscopy, Electron, Transmission
/ Ovule - metabolism
/ Ovule - ultrastructure
/ Petunia - metabolism
/ Petunia - ultrastructure
/ Plant Proteins - metabolism
/ Pollination
/ Time Factors
2015
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Calreticulin expression in relation to exchangeable Ca(2+) level that changes dynamically during anthesis, progamic phase, and double fertilization in Petunia
by
Lenartowski, Robert
, Suwińska, Anna
, Lenartowska, Marta
in
Blotting, Western
/ Calcium - metabolism
/ Calreticulin - metabolism
/ Calreticulin - ultrastructure
/ Fertilization
/ Flowers - metabolism
/ Flowers - ultrastructure
/ Kinetics
/ Microscopy, Electron, Transmission
/ Ovule - metabolism
/ Ovule - ultrastructure
/ Petunia - metabolism
/ Petunia - ultrastructure
/ Plant Proteins - metabolism
/ Pollination
/ Time Factors
2015
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Calreticulin expression in relation to exchangeable Ca(2+) level that changes dynamically during anthesis, progamic phase, and double fertilization in Petunia
by
Lenartowski, Robert
, Suwińska, Anna
, Lenartowska, Marta
in
Blotting, Western
/ Calcium - metabolism
/ Calreticulin - metabolism
/ Calreticulin - ultrastructure
/ Fertilization
/ Flowers - metabolism
/ Flowers - ultrastructure
/ Kinetics
/ Microscopy, Electron, Transmission
/ Ovule - metabolism
/ Ovule - ultrastructure
/ Petunia - metabolism
/ Petunia - ultrastructure
/ Plant Proteins - metabolism
/ Pollination
/ Time Factors
2015
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Calreticulin expression in relation to exchangeable Ca(2+) level that changes dynamically during anthesis, progamic phase, and double fertilization in Petunia
Journal Article
Calreticulin expression in relation to exchangeable Ca(2+) level that changes dynamically during anthesis, progamic phase, and double fertilization in Petunia
2015
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Overview
Calcium (Ca(2+)) plays essential roles in plant sexual reproduction, but the sites and the mechanism of Ca(2+) mobile storage during pollen-pistil interactions have not been fully defined. Because the Ca(2+)-buffering protein calreticulin (CRT) is able to bind and sequester Ca(2+), it can serve as a mobile intracellular store of easily releasable Ca(2+) and control its local concentration within the cytoplasm. Our previous studies showed an enhanced expression of Petunia hybrida CRT gene (PhCRT) during pistil transmitting tract maturation, pollen germination and tube outgrowth on the stigma, gamete fusion, and early embryogenesis. Here, we demonstrate that elevated expression of CRT results in the accumulation of this protein in response to anthesis, pollination, sperm cells deposition within the receptive synergid and fertilization, when the level of exchangeable Ca(2+) changes dynamically. CRT localizes mainly to the endoplasmic reticulum and Golgi compartments in the pistil transmitting tract cells, germinated pollen/tubes, and sporophytic/gametophytic cells of the ovule and corresponds with loosely bound Ca(2+). Additionally, the immunogold research shows, for the first time, highly selective CRT distribution in specific nuclear sub-domains. On the basis of our results, we discuss the possible functions of CRT with respect to the critical role of Ca(2+) homeostasis during key events of the multi-step process of generative reproduction in angiosperms.
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