Literature DB >> 2417231

Behavior of centrosomes during fertilization and cell division in mouse oocytes and in sea urchin eggs.

H Schatten, G Schatten, D Mazia, R Balczon, C Simerly.   

Abstract

The forms and locations of centrosomes in mouse oocytes and in sea urchin eggs were followed through the whole course of fertilization and first cleavage by immunofluorescence microscopy. Centrosomes were identified with an autoimmune antiserum to centrosomal material. Staining of the same preparations with tubulin antibody and with the DNA dye Hoechst 33258 allowed the correlation of the forms of the centrosomes with the microtubule structures that they generate and with the stages of meiosis, syngamy, and mitosis. The results with sea urchin eggs conform to Boveri's view on the paternal origin of the functional centrosomes. Centrosomes are seen in spermatozoa and enter the egg at fertilization. Initially, the centrosomes are compact, but as the eggs enter the mitotic cycle the forms of the centrosomes go through a cycle in which they spread during interphase, apparently divide, and condense into two compact poles by metaphase. In anaphase, they spread to form flat poles. In telophase and during reconstitution of the daughter nuclei, the centrosomal material is disposed as hemispherical caps around the poleward surfaces of the nuclei. Mouse sperm lack centrosomal antigen. In the unfertilized mouse oocyte, the meiotic spindle poles are displayed as broad-beaded centrosomes. In addition, centrosomal material is detected in the cytoplasm as particles, about 16 in number, which are foci of small aster-like arrays of microtubules. The length and number of astral microtubules correlate with the size of the centrosomal foci. After sperm incorporation, as the pronuclei develop and more cytoplasmic microtubules assemble, a few of the foci associate with the peripheries of the nuclei. The number of foci multiplies during the first cell cycle. At the end of interphase, all of the centrosomal foci have concentrated on the nuclear peripheries and the cytoplasmic microtubules have disappeared. At prophase, the centrosomes are seen as two irregular clusters, marking the poles which, at metaphase and anaphase, appear as rough bands with foci, and the spindle is typically barrel-shaped. At telophase, the centrosomes are seen as arcs that lie on the nuclear peripheries after cleavage. The ordering of microtubules in all the stages reflects the shapes of the centrosomes. The findings on the sea urchin confirm the classical theory of the paternal origin of centrosomes and contrast with observations tracing the mitotic poles of the mouse egg to maternal centrosomal material. This evidence strengthens the conclusion that mouse centrosomes derive from the oocyte.

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Year:  1986        PMID: 2417231      PMCID: PMC322800          DOI: 10.1073/pnas.83.1.105

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  20 in total

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Journal:  Cold Spring Harb Symp Quant Biol       Date:  1982

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Journal:  Cold Spring Harb Symp Quant Biol       Date:  1982

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Authors:  L Gerace; G Blobel
Journal:  Cell       Date:  1980-01       Impact factor: 41.582

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Journal:  Eur J Cell Biol       Date:  1982-08       Impact factor: 4.492

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Journal:  J Cell Biol       Date:  1977-06       Impact factor: 10.539

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  58 in total

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Authors:  E N Bocharova; R A Abdumalikov; E E Bragina; R R Klimova; S M Adueva; M G Medzhidova; L F Kurilo; A A Kushch
Journal:  Dokl Biol Sci       Date:  2003 Jul-Aug

2.  Axon selection: From a polarized cytoplasm to a migrating neuron.

Authors:  Froylan Calderon de Anda; Li-Huei Tsai
Journal:  Commun Integr Biol       Date:  2011-05-01

3.  Centrioles in the beginning of human development.

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Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-01       Impact factor: 11.205

4.  Evaluation of maturation competence of metaphase II oocytes in mice based on the distance between pericentriolar materials of meiotic spindle: distance of PCM during oocyte maturation.

Authors:  Chizuka Sakai; Yumi Hoshino; Yusuke Sato; Eimei Sato
Journal:  J Assist Reprod Genet       Date:  2010-11-17       Impact factor: 3.412

Review 5.  The dynamic cytoskeleton of the developing male germ cell.

Authors:  Ann O Sperry
Journal:  Biol Cell       Date:  2012-03-14       Impact factor: 4.458

Review 6.  Maternal control of early mouse development.

Authors:  Lei Li; Ping Zheng; Jurrien Dean
Journal:  Development       Date:  2010-03       Impact factor: 6.868

7.  Isolated Plant Nuclei Nucleate Microtubule Assembly: The Nuclear Surface in Higher Plants Has Centrosome-like Activity.

Authors:  V. Stoppin; M. Vantard; A. C. Schmit; A. M. Lambert
Journal:  Plant Cell       Date:  1994-08       Impact factor: 11.277

8.  Bipolar, anastral spindle development in artificially activated sea urchin eggs.

Authors:  John H Henson; Christopher A Fried; Mary K McClellan; Jason Ader; Jessica E Davis; Rudolf Oldenbourg; Calvin R Simerly
Journal:  Dev Dyn       Date:  2008-05       Impact factor: 3.780

9.  Dephosphorylation of sperm midpiece antigens initiates aster formation in rabbit oocytes.

Authors:  C Pinto-Correia; D L Poccia; T Chang; J M Robl
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-16       Impact factor: 11.205

10.  Effects of activation on functional aster formation, microtubule assembly, and blastocyst development of goat oocytes injected with round spermatids.

Authors:  Xin-Yong Liu; Yi-Long Miao; Jie Zhang; Jian-Hua Qiu; Xiang-Zhong Cui; Wei-Qiang Gao; Ming-Jiu Luo; Jing-He Tan
Journal:  Cell Reprogram       Date:  2012-08-21       Impact factor: 1.987

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