|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 105, Issue 2 237-249, Copyright © 1989 by Company of Biologists
JOURNAL ARTICLES |
C Sardet, J Speksnijder, S Inoue and L Jaffe
Unite de Biologie Cellulaire Marine CNRS/Paris VI, Villfranche-sur-mer, France.
Using light microscopy techniques, we have studied the movements that follow fertilization in the denuded egg of the ascidian Phallusia mammillata. In particular, our observations show that, as a result of a series of movements described below, the mitochondria-rich subcortical myoplasm is split in two parts during the second phase of ooplasmic segregation. This offers a potential explanation for the origin of larval muscle cells from both posterior and anterior blastomeres. The first visible event at fertilization is a bulging at the animal pole of the egg, which is immediately followed by a wave of contraction, travelling towards the vegetal pole with a surface velocity of 1.4 microns s-1. This wave accompanies the first phase of ooplasmic segregation of the mitochondria-rich subcortical myoplasm. After this contraction wave has reached the vegetal pole after about 2 min, a transient cytoplasmic lobe remains there until 6 min after fertilization. Several new features of the morphogenetic movements were then observed: between the extrusion of the first and second polar body (at 5 and 24-29 min, respectively), a series of transient animal protrusions form at regular intervals. Each animal protrusion involves a flow of the centrally located cytoplasm in the animal direction. Shortly before the second polar body is extruded, a second transient vegetal lobe ('the vegetal button') forms, which, like the first, resembles a protostome polar lobe. Immediately after the second polar body is extruded, three events occur almost simultaneously: first, the sperm aster moves from the vegetal hemisphere to the equator. Second, the bulk of the vegetally located myoplasm moves with the sperm aster towards the future posterior pole, but interestingly about 20% remains behind at the anterior side of the embryo. This second phase of myoplasmic movement shows two distinct subphases: a first, oscillatory subphase with an average velocity of about 6 microns min-1, and a second steady subphase with a velocity of about 26 microns min-1. The myoplasm reaches its final position as the male pronucleus with its surrounding aster moves towards the centre of the egg. Third, the female pronucleus moves towards the centre of the egg to meet with the male pronucleus. Like the myoplasm, the migrations of both the sperm aster and the female pronucleus shows two subphases with distinctly different velocities. Finally, the pronuclear membranes dissolve, a small mitotic spindle is formed with very large asters, and at about 60-65 min after fertilization, the egg cleaves.
This article has been cited by other articles:
![]() |
F. Prodon, P. Dru, F. Roegiers, and C. Sardet Polarity of the ascidian egg cortex and relocalization of cER and mRNAs in the early embryo J. Cell Sci., June 1, 2005; 118(11): 2393 - 2404. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. L. Russo, M. Tosto, A. Mupo, I. Castellano, A. Cuomo, and E. Tosti Biochemical and Functional Characterization of Protein Kinase CK2 in Ascidian Ciona intestinalis Oocytes at Fertilization: CLONING AND SEQUENCE ANALYSIS OF cDNA FOR {alpha} AND {beta} SUBUNITS J. Biol. Chem., July 30, 2004; 279(31): 33012 - 33023. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Sardet, H. Nishida, F. Prodon, and K. Sawada Maternal mRNAs of PEM and macho 1, the ascidian muscle determinant, associate and move with a rough endoplasmic reticulum network in the egg cortex Development, December 1, 2003; 130(23): 5839 - 5849. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Piotrowska and M. Zernicka-Goetz Early patterning of the mouse embryo -- contributions of sperm and egg Development, March 14, 2003; 129(24): 5803 - 5813. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Dumollard and C. Sardet Three different calcium wave pacemakers in ascidian eggs J. Cell Sci., January 7, 2001; 114(13): 2471 - 2481. [Abstract] [Full Text] [PDF] |
||||
![]() |
A McDougall, M Levasseur, A. O'Sullivan, and K. Jones Cell cycle-dependent repetitive Ca(2+ )waves induced by a cytosolic sperm extract in mature ascidian eggs mimic those observed at fertilization J. Cell Sci., January 10, 2000; 113(19): 3453 - 3462. [Abstract] [PDF] |
||||
![]() |
M Levasseur and A McDougall Sperm-induced calcium oscillations at fertilisation in ascidians are controlled by cyclin B1-dependent kinase activity Development, January 2, 2000; 127(3): 631 - 641. [Abstract] [PDF] |
||||
![]() |
F Roegiers, C Djediat, R Dumollard, C Rouviere, and C Sardet Phases of cytoplasmic and cortical reorganizations of the ascidian zygote between fertilization and first division Development, January 6, 1999; 126(14): 3101 - 3117. [Abstract] [PDF] |
||||
![]() |
M. Albrieux, H. C. Lee, and M. Villaz Calcium Signaling by Cyclic ADP-ribose, NAADP, and Inositol Trisphosphate Are Involved in Distinct Functions in Ascidian Oocytes J. Biol. Chem., June 5, 1998; 273(23): 14566 - 14574. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. TAKAHASHI and Y. OKAMURA Ion Channels and Early Development of Neural Cells Physiol Rev, April 1, 1998; 78(2): 307 - 337. [Abstract] [Full Text] [PDF] |
||||
![]() |
H Eyal-Giladi Establishment of the axis in chordates: facts and speculations Development, January 6, 1997; 124(12): 2285 - 2296. [Abstract] [PDF] |
||||
![]() |
G. Russo, K Kyozuka, L Antonazzo, E Tosti, and B Dale Maturation promoting factor in ascidian oocytes is regulated by different intracellular signals at meiosis I and II Development, January 7, 1996; 122(7): 1995 - 2003. [Abstract] [PDF] |
||||
![]() |
H Nishida Vegetal egg cytoplasm promotes gastrulation and is responsible for specification of vegetal blastomeres in embryos of the ascidian Halocynthia roretzi Development, January 4, 1996; 122(4): 1271 - 1279. [Abstract] [PDF] |
||||
![]() |
C. Larabell, B. Rowning, J Wells,, M Wu, and J. Gerhart Confocal microscopy analysis of living Xenopus eggs and the mechanism of cortical rotation Development, January 4, 1996; 122(4): 1281 - 1289. [Abstract] [PDF] |
||||
![]() |
F Roegiers, A McDougall, and C Sardet The sperm entry point defines the orientation of the calcium-induced contraction wave that directs the first phase of cytoplasmic reorganization in the ascidian egg Development, January 10, 1995; 121(10): 3457 - 3466. [Abstract] [PDF] |
||||