Literature DB >> 8449980

Polarity and reorganization of the endoplasmic reticulum during fertilization and ooplasmic segregation in the ascidian egg.

J E Speksnijder1, M Terasaki, W J Hage, L F Jaffe, C Sardet.   

Abstract

During the first cell cycle of the ascidian egg, two phases of ooplasmic segregation create distinct cytoplasmic domains that are crucial for later development. We recently defined a domain enriched in ER in the vegetal region of Phallusia mammillata eggs. To explore the possible physiological and developmental function of this ER domain, we here investigate its organization and fate by labeling the ER network in vivo with DiIC16(3), and observing its distribution before and after fertilization in the living egg. In unfertilized eggs, the ER-rich vegetal cortex is overlaid by the ER-poor but mitochondria-rich subcortical myoplasm. Fertilization results in striking rearrangements of the ER network. First, ER accumulates at the vegetal-contraction pole as a thick layer between the plasma membrane and the myoplasm. This accompanies the relocation of the myoplasm toward that region during the first phase of ooplasmic segregation. In other parts of the cytoplasm, ER becomes progressively redistributed into ER-rich and ER-poor microdomains. As the sperm aster grows, ER accumulates in its centrosomal area and along its astral rays. During the second phase of ooplasmic segregation, which takes place once meiosis is completed, the concentrated ER domain at the vegetal-contraction pole moves with the sperm aster and the bulk of the myoplasm toward the future posterior side of the embryo. These results show that after fertilization, ER first accumulates in the vegetal area from which repetitive calcium waves are known to originate (Speksnijder, J. E. 1992. Dev. Biol. 153:259-271). This ER domain subsequently colocalizes with the myoplasm to the presumptive primary muscle cell region.

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Year:  1993        PMID: 8449980      PMCID: PMC2119754          DOI: 10.1083/jcb.120.6.1337

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  46 in total

1.  Ultraviolet irradiation during ooplasmic segregation prevents gastrulation, sensory cell induction, and axis formation in the ascidian embryo.

Authors:  W R Jeffery
Journal:  Dev Biol       Date:  1990-08       Impact factor: 3.582

2.  Identification of a calsequestrin-like protein from sea urchin eggs.

Authors:  J A Oberdorf; D Lebeche; J F Head; B Kaminer
Journal:  J Biol Chem       Date:  1988-05-15       Impact factor: 5.157

3.  Localization of endoplasmic reticulum in living and glutaraldehyde-fixed cells with fluorescent dyes.

Authors:  M Terasaki; J Song; J R Wong; M J Weiss; L B Chen
Journal:  Cell       Date:  1984-08       Impact factor: 41.582

4.  Microinjection of echinoderm eggs: apparatus and procedures.

Authors:  D P Kiehart
Journal:  Methods Cell Biol       Date:  1982       Impact factor: 1.441

5.  Characterization of sea urchin egg endoplasmic reticulum in cortical preparations.

Authors:  M Terasaki; J Henson; D Begg; B Kaminer; C Sardet
Journal:  Dev Biol       Date:  1991-11       Impact factor: 3.582

6.  Uptake and release of calcium by isolated egg cortices of the sea urchin Paracentrotus lividus.

Authors:  P Payan; J P Girard; C Sardet; M Whitaker; J Zimmerberg
Journal:  Biol Cell       Date:  1986       Impact factor: 4.458

7.  Fertilization and ooplasmic movements in the ascidian egg.

Authors:  C Sardet; J Speksnijder; S Inoue; L Jaffe
Journal:  Development       Date:  1989-02       Impact factor: 6.868

8.  Evidence for the involvement of microtubules, ER, and kinesin in the cortical rotation of fertilized frog eggs.

Authors:  E Houliston; R P Elinson
Journal:  J Cell Biol       Date:  1991-09       Impact factor: 10.539

9.  Construction of the endoplasmic reticulum.

Authors:  C Lee; M Ferguson; L B Chen
Journal:  J Cell Biol       Date:  1989-11       Impact factor: 10.539

10.  Dynactin, a conserved, ubiquitously expressed component of an activator of vesicle motility mediated by cytoplasmic dynein.

Authors:  S R Gill; T A Schroer; I Szilak; E R Steuer; M P Sheetz; D W Cleveland
Journal:  J Cell Biol       Date:  1991-12       Impact factor: 10.539

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  6 in total

1.  Changes in organization of the endoplasmic reticulum during Xenopus oocyte maturation and activation.

Authors:  M Terasaki; L L Runft; A R Hand
Journal:  Mol Biol Cell       Date:  2001-04       Impact factor: 4.138

Review 2.  Calcium at fertilization and in early development.

Authors:  Michael Whitaker
Journal:  Physiol Rev       Date:  2006-01       Impact factor: 37.312

3.  Cell cycle-dependent regulation of structure of endoplasmic reticulum and inositol 1,4,5-trisphosphate-induced Ca2+ release in mouse oocytes and embryos.

Authors:  Greg FitzHarris; Petros Marangos; John Carroll
Journal:  Mol Biol Cell       Date:  2003-01       Impact factor: 4.138

Review 4.  Calcium signalling in early embryos.

Authors:  Michael Whitaker
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-04-12       Impact factor: 6.237

5.  A cleavage clock regulates features of lineage-specific differentiation in the development of a basal branching metazoan, the ctenophore Mnemiopsis leidyi.

Authors:  Antje Hl Fischer; Kevin Pang; Jonathan Q Henry; Mark Q Martindale
Journal:  Evodevo       Date:  2014-01-31       Impact factor: 2.250

6.  Dynamic changes in the association between maternal mRNAs and endoplasmic reticulum during ascidian early embryogenesis.

Authors:  Toshiyuki Goto; Shuhei Torii; Aoi Kondo; Junji Kawakami; Haruka Yagi; Masato Suekane; Yosky Kataoka; Takahito Nishikata
Journal:  Dev Genes Evol       Date:  2021-12-18       Impact factor: 0.900

  6 in total

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