Literature DB >> 8804312

Oskar protein interaction with Vasa represents an essential step in polar granule assembly.

W Breitwieser1, F H Markussen, H Horstmann, A Ephrussi.   

Abstract

The posterior pole plasm of the Drosophila egg contains the determinants of abdominal and germ-cell fates of the embryo. Pole plasm assembly is induced by oskar RNA localized to the posterior pole of the oocyte. Genetics has revealed three additional genes, staufen, vasa, and tudor, that are also essential for pole plasm formation. Staufen protein is required for both oskar RNA localization and translation. Vasa and Tudor are localized dependent on Oskar protein and are required to accumulate Oskar protein stably at the posterior pole. We have explored interactions between these gene products at the molecular level and find that Oskar interacts directly with Vasa and Staufen, in a yeast two-hybrid assay. These interactions also occur in vitro and are affected by mutations in Oskar that abolish pole plasm formation in vivo. Finally, we show that in the pole plasm, Oskar protein, like Vasa and Tudor, is a component of polar granules, the germ-line-specific RNP structures. These results suggest that the Oskar-Vasa interaction constitutes an initial step in polar granule assembly. In addition, we discuss the possible biological role of the Oskar-Staufen interaction.

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Year:  1996        PMID: 8804312     DOI: 10.1101/gad.10.17.2179

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  73 in total

Review 1.  New insights into the regulation of RNP granule assembly in oocytes.

Authors:  Jennifer A Schisa
Journal:  Int Rev Cell Mol Biol       Date:  2012       Impact factor: 6.813

2.  Sm proteins specify germ cell fate by facilitating oskar mRNA localization.

Authors:  Graydon B Gonsalvez; T K Rajendra; Ying Wen; Kavita Praveen; A Gregory Matera
Journal:  Development       Date:  2010-07       Impact factor: 6.868

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

Authors:  Eric A Gustafson; Gary M Wessel
Journal:  Bioessays       Date:  2010-07       Impact factor: 4.345

4.  A conserved germline multipotency program.

Authors:  Celina E Juliano; S Zachary Swartz; Gary M Wessel
Journal:  Development       Date:  2010-12       Impact factor: 6.868

5.  Identification of X-linked genes required for migration and programmed cell death of Drosophila melanogaster germ cells.

Authors:  Clark R Coffman; Rachel C Strohm; Fredrick D Oakley; Yukiko Yamada; Danielle Przychodzin; Robert E Boswell
Journal:  Genetics       Date:  2002-09       Impact factor: 4.562

6.  A late phase of germ plasm accumulation during Drosophila oogenesis requires lost and rumpelstiltskin.

Authors:  Kristina S Sinsimer; Roshan A Jain; Seema Chatterjee; Elizabeth R Gavis
Journal:  Development       Date:  2011-07-13       Impact factor: 6.868

7.  C-terminal residues specific to Vasa among DEAD-box helicases are required for its functions in piRNA biogenesis and embryonic patterning.

Authors:  Mehrnoush Dehghani; Paul Lasko
Journal:  Dev Genes Evol       Date:  2016-08-29       Impact factor: 0.900

Review 8.  Lessons for inductive germline determination.

Authors:  Riyad N H Seervai; Gary M Wessel
Journal:  Mol Reprod Dev       Date:  2013-02-28       Impact factor: 2.609

9.  Arginine methylation of vasa protein is conserved across phyla.

Authors:  Yohei Kirino; Anastassios Vourekas; Namwoo Kim; Flavia de Lima Alves; Juri Rappsilber; Peter S Klein; Thomas A Jongens; Zissimos Mourelatos
Journal:  J Biol Chem       Date:  2010-01-15       Impact factor: 5.157

10.  Sequence-Independent Self-Assembly of Germ Granule mRNAs into Homotypic Clusters.

Authors:  Tatjana Trcek; Tyler E Douglas; Markus Grosch; Yandong Yin; Whitby V I Eagle; Elizabeth R Gavis; Hari Shroff; Eli Rothenberg; Ruth Lehmann
Journal:  Mol Cell       Date:  2020-05-27       Impact factor: 17.970

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