Literature DB >> 9927594

Binuclear Drosophila oocytes: consequences and implications for dorsal-ventral patterning in oogenesis and embryogenesis.

S Roth1, P Jordan, R Karess.   

Abstract

The position of the nucleus along the anterior rim of stage 8 Drosophila oocytes presages the dorsal side of the egg and the developing embryo. In this paper, we address the question of whether the oocyte has a previously determined dorsal side to which the nucleus is drawn, or whether nuclear position randomly determines the dorsal side. To do so, we have taken advantage of a genetic system in which Drosophila oocytes occasionally become binuclear. We find that (i) the two nuclei migrate independently to their respective positions on the anterior rim, sometimes selecting the same site, sometimes not, (ii) the two nuclei are equivalent in their ability to induce a dorsal-ventral pattern in the overlying follicular epithelium, and (iii) at any position around the anterior circumference of the egg chamber the follicle cell sheet is equally responsive to the Gurken signal associated with the oocyte nuclei. These results argue that the dorsal-ventral axis is determined arbitrarily by the randomly selected position of the nucleus on the anterior rim of the oocyte. Some of the binuclear eggs support embryonic development. However, despite the duplication of dorsal chorion structures, the majority of such embryos show normal dorsal-ventral patterning. Thus, processes exist in the ventral follicular epithelium or in the perivitelline space that compensate for the expansion of dorsal follicle cell fates and consequently allow the formation of a normal embryonic axis.

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Year:  1999        PMID: 9927594     DOI: 10.1242/dev.126.5.927

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


  10 in total

1.  The origin of dorsoventral polarity in Drosophila.

Authors:  Siegfried Roth
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-08-29       Impact factor: 6.237

Review 2.  Symmetry breaking during Drosophila oogenesis.

Authors:  Siegfried Roth; Jeremy A Lynch
Journal:  Cold Spring Harb Perspect Biol       Date:  2009-08       Impact factor: 10.005

Review 3.  Maternal control of the Drosophila dorsal-ventral body axis.

Authors:  David S Stein; Leslie M Stevens
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2014-05-29       Impact factor: 5.814

4.  Drosophila variable nurse cells encodes arrest defective 1 (ARD1), the catalytic subunit of the major N-terminal acetyltransferase complex.

Authors:  Ying Wang; Michelle Mijares; Megan D Gall; Tolga Turan; Anna Javier; Douglas J Bornemann; Kevin Manage; Rahul Warrior
Journal:  Dev Dyn       Date:  2010-11       Impact factor: 3.780

Review 5.  Polarity Events in the Drosophila melanogaster Oocyte.

Authors:  Ana Milas; Ivo A Telley
Journal:  Front Cell Dev Biol       Date:  2022-05-05

6.  Posterior localization of dynein and dorsal-ventral axis formation depend on kinesin in Drosophila oocytes.

Authors:  Robert P Brendza; Laura R Serbus; William M Saxton; Joseph B Duffy
Journal:  Curr Biol       Date:  2002-09-03       Impact factor: 10.834

7.  gamma-Tubulin function during female germ-cell development and oogenesis in Drosophila.

Authors:  Gaia Tavosanis; Cayetano Gonzalez
Journal:  Proc Natl Acad Sci U S A       Date:  2003-08-12       Impact factor: 11.205

8.  Molecular mechanisms of EGF signaling-dependent regulation of pipe, a gene crucial for dorsoventral axis formation in Drosophila.

Authors:  Martin Technau; Meike Knispel; Siegfried Roth
Journal:  Dev Genes Evol       Date:  2011-12-24       Impact factor: 0.900

9.  Distinct molecular cues ensure a robust microtubule-dependent nuclear positioning in the Drosophila oocyte.

Authors:  Nicolas Tissot; Jean-Antoine Lepesant; Fred Bernard; Kevin Legent; Floris Bosveld; Charlotte Martin; Orestis Faklaris; Yohanns Bellaïche; Maïté Coppey; Antoine Guichet
Journal:  Nat Commun       Date:  2017-04-27       Impact factor: 14.919

10.  Co-option of a coordinate system defined by the EGFr and Dpp pathways in the evolution of a morphological novelty.

Authors:  Barbara Mi Vreede; Jeremy A Lynch; Siegfried Roth; Elio Sucena
Journal:  Evodevo       Date:  2013-03-01       Impact factor: 2.250

  10 in total

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