Literature DB >> 2384213

Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development.

P F Lasko1, M Ashburner.   

Abstract

The protein product of the Drosophila maternal-effect posterior group gene vasa is localized to the posterior pole of the oocyte and is sequestered by the pole cells as they form. It is, however, present at easily detectable levels throughout the oocyte and pre-blastoderm embryo. The protein is present in the pole cells and their germ line derivatives throughout all stages of development. An antiserum against this protein recognizes a pole-cell-specific antigen in seven other Drosophila species. Of six other maternal-effect loci essential for embryonic pole cell development, none affects expression of vasa, mutations in four abolish vasa protein localization, and mutations in two, tudor and valois, have little, if any, effect on vasa expression or localization. This indicates that vasa protein, when properly localized, is not sufficient for induction of pole cell development, and that at least the tudor and valois wild-type functions are also required specifically for this process. These results are discussed with respect to the multiple functions of the vasa gene.

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Year:  1990        PMID: 2384213     DOI: 10.1101/gad.4.6.905

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


  99 in total

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2.  The posterior determinant gene nanos is required for the maintenance of the adult germline stem cells during Drosophila oogenesis.

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8.  Sex-lethal facilitates the transition from germline stem cell to committed daughter cell in the Drosophila ovary.

Authors:  Johnnie Chau; Laura Shapiro Kulnane; Helen K Salz
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9.  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

10.  Vasa promotes Drosophila germline stem cell differentiation by activating mei-P26 translation by directly interacting with a (U)-rich motif in its 3' UTR.

Authors:  Niankun Liu; Hong Han; Paul Lasko
Journal:  Genes Dev       Date:  2009-12-01       Impact factor: 11.361

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