Literature DB >> 509523

After fertilization, sperm surface components remain as a patch in sea urchin and mouse embryos.

C A Gabel, E M Eddy, B M Shapiro.   

Abstract

Sea urchin and mouse sperm that are labeled on their surfaces with fluorescein isothiocyanate (FITC), tetramethylrhodamine isothiocyanate (TMRTC) or 125I-diiodofluorescein isothiocyanate (125IFC) remain viable and can fertilize eggs. When sea urchin eggs were fertilized with 125IFC-labeled sperm, the radioactivity from the sperm was quantitatively transferred to the egg (at a ratio of one sperm equivalent per egg) and persisted in the embryo as it developed to the pluteus larval state (5 days at 12 degrees C). The radioactivity was acid-precipitable and was associated with the particulate fraction of embryo homogenates. In addition, FITC-labeled sea urchin sperm were used to fertilize eggs, and the labeled components were followed by fluorescence microscopy. In the embryo, labeled sperm components were present as a discrete patch that was partitioned unequally during early cleavages. In experiments using mouse sperm labeled with TMRTC, the labeled sperm components were also transferred to the embryo as a discrete patch that was again distributed unequally after cleavage. This physiological cell fusion system therefore has distinctive characteristics: there is limited lateral mobility of surface components, which have a low turnover rate unlike that see in other systems. In this paper, we discussed the possible morphogenetic role of this unusual behavior.

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Year:  1979        PMID: 509523     DOI: 10.1016/0092-8674(79)90369-6

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  7 in total

1.  Expression of envelope proteins of endogeneous C-type retrovirus on the surface of mouse and human oocytes at fertilization.

Authors:  B O Nilsson; M Jin; A C Andersson; P Sundström; E Larsson
Journal:  Virus Genes       Date:  1999       Impact factor: 2.332

2.  Voltage-clamp study of the conductance activated at fertilization in the starfish egg.

Authors:  J B Lansman
Journal:  J Physiol       Date:  1983-12       Impact factor: 5.182

3.  Full-term development after transplantation of parthenogenetic embryonic nuclei into fertilized mouse eggs.

Authors:  P C Hoppe; K Illmensee
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

4.  Capsid protein-encoding genes of hamster polyomavirus and properties of the viral capsid.

Authors:  H Siray; M Ozel; B Jandrig; T Voronkova; W Jia; R Zocher; W Arnold; S Scherneck; D H Krüger; R Ulrich
Journal:  Virus Genes       Date:  1999       Impact factor: 2.332

5.  The use of fluorescein isothiocyanate (FITC) as a short-term cell lineage marker in the peri-implantation mouse embryo.

Authors:  Carol Ann Ziomek
Journal:  Wilehm Roux Arch Dev Biol       Date:  1982-01

6.  Identification of a paternal developmental effect on the cytoplasm of one-cell-stage mouse embryos.

Authors:  J P Renard; C Babinet
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

7.  Sperm surface proteins persist after fertilization.

Authors:  G G Gundersen; B M Shapiro
Journal:  J Cell Biol       Date:  1984-10       Impact factor: 10.539

  7 in total

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