Literature DB >> 9806928

Fertile offspring derived from mammalian eggs lacking either animal or vegetal poles.

M Zernicka-Goetz1.   

Abstract

In all animals so far tested, removing either pole of the undivided egg prevents normal development: embryos may arrest early, lack organs, or the adults may be sterile. These experiments have shown that spatial patterning of the egg is of utmost importance for subsequent development. However, the significance of spatial patterning in mammalian eggs is still controversial. To test the importance of egg polarity in the mouse a substantial amount of material either from the animal (polar body-associated) or the vegetal (opposite) pole of the fertilised egg was removed. One pole of the egg was cut away manually with a glass needle and the eggs were allowed to develop in vitro. Both kinds of surgical operation permit the development of blastocysts, which, after transfer to the uteri of pseudo-pregnant foster mothers, can produce viable offspring. Furthermore, these develop into fertile adult mice. I conclude that mouse eggs have no essential components that are localised uniquely to the animal or the vegetal pole and, therefore, do not rely for their axial development on maternal determinants that are so localised in the fertilised egg. Thus the mammalian egg appears to be very unusual in the animal kingdom in that it establishes the embryonic axes after the zygote has begun development.

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Year:  1998        PMID: 9806928     DOI: 10.1242/dev.125.23.4803

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  13 in total

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Journal:  J Reprod Dev       Date:  2003-12-01       Impact factor: 2.214

2.  A zebrafish nanos-related gene is essential for the development of primordial germ cells.

Authors:  M Köprunner; C Thisse; B Thisse; E Raz
Journal:  Genes Dev       Date:  2001-11-01       Impact factor: 11.361

3.  Developmental clock and mechanism of de novo polarization of the mouse embryo.

Authors:  Meng Zhu; Jake Cornwall-Scoones; Peizhe Wang; Charlotte E Handford; Jie Na; Matt Thomson; Magdalena Zernicka-Goetz
Journal:  Science       Date:  2020-12-11       Impact factor: 47.728

Review 4.  The function and regulation of vasa-like genes in germ-cell development.

Authors:  E Raz
Journal:  Genome Biol       Date:  2000-09-01       Impact factor: 13.583

5.  The mouse homolog of Drosophila Vasa is required for the development of male germ cells.

Authors:  S S Tanaka; Y Toyooka; R Akasu; Y Katoh-Fukui; Y Nakahara; R Suzuki; M Yokoyama; T Noce
Journal:  Genes Dev       Date:  2000-04-01       Impact factor: 11.361

Review 6.  Early human development: new data raise important embryological and ethical questions relevant for stem cell research.

Authors:  Hans-Werner Denker
Journal:  Naturwissenschaften       Date:  2003-12-18

7.  Distribution of RNA binding protein MOEP19 in the oocyte cortex and early embryo indicates pre-patterning related to blastomere polarity and trophectoderm specification.

Authors:  John C Herr; Olga Chertihin; Laura Digilio; Kula N Jha; Soumya Vemuganti; Charles J Flickinger
Journal:  Dev Biol       Date:  2007-12-04       Impact factor: 3.582

8.  Developmental bias in cleavage-stage mouse blastomeres.

Authors:  Inna Tabansky; Alan Lenarcic; Ryan W Draft; Karine Loulier; Derin B Keskin; Jacqueline Rosains; José Rivera-Feliciano; Jeff W Lichtman; Jean Livet; Joel N H Stern; Joshua R Sanes; Kevin Eggan
Journal:  Curr Biol       Date:  2012-11-21       Impact factor: 10.834

9.  Subcellular distribution of mitochondrial ribosomal RNA in the mouse oocyte and zygote.

Authors:  Youichirou Ninomiya; Shizuko Ichinose
Journal:  PLoS One       Date:  2007-11-28       Impact factor: 3.240

10.  Understanding the molecular circuitry of cell lineage specification in the early mouse embryo.

Authors:  Anna Bergsmedh; Mary E Donohoe; Rebecca-Ayme Hughes; Anna-Katerina Hadjantonakis
Journal:  Genes (Basel)       Date:  2011-07-13       Impact factor: 4.096

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