Literature DB >> 2119289

Localization of vasa, a component of Drosophila polar granules, in maternal-effect mutants that alter embryonic anteroposterior polarity.

B Hay1, L Y Jan, Y N Jan.   

Abstract

Cytoplasm at the posterior pole of the early Drosophila embryo, known as polar plasm, serves as a source of information necessary for germ cell determination and for specification of the abdominal region. Likely candidates for cytoplasmic elements important in one or both of these processes are polar granules, organelles concentrated in the cortical cytoplasm of the posterior pole. Females homozygous for any one of the maternal-effect mutations, tudor, oskar, staufen, vasa, or valois give rise to embryos that lack localized polar granules, fail to form the germ cell lineage and have abdominal segment deletions. Using antibodies against a polar granule component, the vasa protein, we find that vasa synthesis or localization is affected by these mutations. In vasa mutants, synthesis of vasa protein is absent or severely restricted. In oskar and staufen mutant females, vasa synthesis appears normal, but the vasa protein is not localized. In tudor and valois mutant females, vasa is localized to the posterior pole of oocytes, but this localization is lost following egg activation. In addition to the posterior localized vasa, there is a low level of vasa distributed throughout the embryo. A function for this distributed vasa is postulated based on the observation that embryos from Bicaudal-D mothers, in which abdominal determinants are incorrectly localized to the anterior pole, do not show any ectopic vasa localization, though abdomen development at the anterior end depends on the amount of vasa protein in the embryo.

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Year:  1990        PMID: 2119289     DOI: 10.1242/dev.109.2.425

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


  51 in total

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Journal:  Genetics       Date:  2003-12       Impact factor: 4.562

2.  Vasa genes: emerging roles in the germ line and in multipotent cells.

Authors:  Eric A Gustafson; Gary M Wessel
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3.  A conserved germline multipotency program.

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Journal:  Development       Date:  2010-12       Impact factor: 6.868

4.  A Drosophila chromatin factor interacts with the Piwi-interacting RNA mechanism in niche cells to regulate germline stem cell self-renewal.

Authors:  Tora K Smulders-Srinivasan; Akos Szakmary; Haifan Lin
Journal:  Genetics       Date:  2010-07-20       Impact factor: 4.562

5.  Post-translational regulation by gustavus contributes to selective Vasa protein accumulation in multipotent cells during embryogenesis.

Authors:  Eric A Gustafson; Mamiko Yajima; Celina E Juliano; Gary M Wessel
Journal:  Dev Biol       Date:  2010-10-28       Impact factor: 3.582

6.  Dynamic Hsp83 RNA localization during Drosophila oogenesis and embryogenesis.

Authors:  D Ding; S M Parkhurst; S R Halsell; H D Lipshitz
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

7.  Drosophila pericentrin-like protein promotes the formation of primordial germ cells.

Authors:  Junnan Fang; Dorothy A Lerit
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Review 8.  A pilgrim's progress: Seeking meaning in primordial germ cell migration.

Authors:  Andrea V Cantú; Diana J Laird
Journal:  Stem Cell Res       Date:  2017-07-18       Impact factor: 2.020

9.  Mouse Germ Cell Development in-vivo and in-vitro.

Authors:  Deshira Saiti; Orly Lacham-Kaplan
Journal:  Biomark Insights       Date:  2007-06-06

10.  The Yb protein defines a novel organelle and regulates male germline stem cell self-renewal in Drosophila melanogaster.

Authors:  Akos Szakmary; Mary Reedy; Hongying Qi; Haifan Lin
Journal:  J Cell Biol       Date:  2009-05-11       Impact factor: 10.539

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