Using the fluorescent dye Calcium Green-dextran, we measured intracellular Ca 2+ in oocytes of the ascidian Ciona intestinalis at fertilization and during progression through meiosis. The relative fluorescence intensity increased shortly after insemination in a single transient, the activation peak, and this was followed by several smaller oscillations that lasted for approximately 5 minutes (phase 1). The first polar body was extruded after the completion of the phase 1 transients, about 9 minutes after insemination, and then the intracellular calcium level remained at baseline for a period of 5 minutes (phase 2). At 14 minutes postinsemination a second series of oscillations was initiated that lasted 11 minutes (phase 3) and terminated at the time of second polar body extrusion. Phases 1 and 3 were inhibited by preloading oocytes with 5 mM heparin. Simultaneous measurements of membrane currents, in the whole-cell clamp configuration, showed that the 1-2 nA inward fertilization current correlated temporally with the activation peak, while a series of smaller oscillations of 0.1-0.3 nA amplitude were generated at the time of the phase 3 oscillations.

Maturation Promoting Factor in ascidian oocytes is regulated by different intracellular signals at meiosis I and II

Russo;G L;
1996

Abstract

Using the fluorescent dye Calcium Green-dextran, we measured intracellular Ca 2+ in oocytes of the ascidian Ciona intestinalis at fertilization and during progression through meiosis. The relative fluorescence intensity increased shortly after insemination in a single transient, the activation peak, and this was followed by several smaller oscillations that lasted for approximately 5 minutes (phase 1). The first polar body was extruded after the completion of the phase 1 transients, about 9 minutes after insemination, and then the intracellular calcium level remained at baseline for a period of 5 minutes (phase 2). At 14 minutes postinsemination a second series of oscillations was initiated that lasted 11 minutes (phase 3) and terminated at the time of second polar body extrusion. Phases 1 and 3 were inhibited by preloading oocytes with 5 mM heparin. Simultaneous measurements of membrane currents, in the whole-cell clamp configuration, showed that the 1-2 nA inward fertilization current correlated temporally with the activation peak, while a series of smaller oscillations of 0.1-0.3 nA amplitude were generated at the time of the phase 3 oscillations.
1996
Istituto di Scienze dell'Alimentazione - ISA
calcium ion
cyclin b
cyclin dependent kinase
dextran
ethylene glycol 1
2 bis(2 aminophenyl) ether n
n
n'
n' tetraacetic acid
fluorescent dye
histone h1
maturation promoting factor
protamine kinase
animal tissue
article
ascidiacea
calcium cell level
cell cycle s phase
chordata
fertilization
meiosis
metaphase
nonhuman
oocyte
oscillation
priority journal
signal transduction
telophase
Amino Acid Sequence
Animals
Calcium
Cell Membrane
Chelating Agents
Ciona intestinalis
Cyclins
Egtazic Acid
Enzyme Activation
Heparin
Maturation-Promoting Factor
Meiosis
Molecular Sequence Data
Oocytes
Protein-Serine-Threonine Kinases
Signal Transduction
Animalia
Ascidia
Ascidiacea
Chordata
Ciona intestinalis
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/206362
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