Literature DB >> 7555702

Localization of oskar RNA regulates oskar translation and requires Oskar protein.

C Rongo1, E R Gavis, R Lehmann.   

Abstract

The site of oskar RNA and protein localization within the oocyte determines where in the embryo primordial germ cells form and where the abdomen develops. Initiation of oskar RNA localization requires the activity of several genes. We show that ovaries mutant for any of these genes lack Oskar protein. Using various transgenic constructs we have determined that sequences required for oskar RNA localization and translational repression map to the oskar 3'UTR, while sequences involved in the correct temporal activation of translation reside outside the oskar 3'UTR. Upon localization of oskar RNA and protein at the posterior pole, Oskar protein is required to maintain localization of oskar RNA throughout oogenesis. Stable anchoring of a transgenic reporter RNA at the posterior pole is disrupted by oskar nonsense mutations. We propose that initially localization of oskar RNA permits translation into Oskar protein and that subsequently Oskar protein regulates its own RNA localization through a positive feedback mechanism.

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Year:  1995        PMID: 7555702     DOI: 10.1242/dev.121.9.2737

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


  65 in total

1.  Distinct roles of two conserved Staufen domains in oskar mRNA localization and translation.

Authors:  D R Micklem; J Adams; S Grünert; D St Johnston
Journal:  EMBO J       Date:  2000-03-15       Impact factor: 11.598

2.  Coordinate control of translation and localization of Vg1 mRNA in Xenopus oocytes.

Authors:  J E Wilhelm; R D Vale; R S Hegde
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

3.  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

4.  Capicua integrates input from two maternal systems in Drosophila terminal patterning.

Authors:  Einat Cinnamon; Devorah Gur-Wahnon; Aharon Helman; Daniel St Johnston; Gerardo Jiménez; Ze'ev Paroush
Journal:  EMBO J       Date:  2004-10-28       Impact factor: 11.598

5.  RNA localization.

Authors:  Yaron Shav-Tal; Robert H Singer
Journal:  J Cell Sci       Date:  2005-09-15       Impact factor: 5.285

6.  Heterogeneous nuclear ribonucleoprotein (hnRNP) E1 binds to hnRNP A2 and inhibits translation of A2 response element mRNAs.

Authors:  Linda D Kosturko; Michael J Maggipinto; George Korza; Joo Won Lee; John H Carson; Elisa Barbarese
Journal:  Mol Biol Cell       Date:  2006-06-14       Impact factor: 4.138

7.  Imp associates with squid and Hrp48 and contributes to localized expression of gurken in the oocyte.

Authors:  Cuiyun Geng; Paul M Macdonald
Journal:  Mol Cell Biol       Date:  2006-10-09       Impact factor: 4.272

8.  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

9.  Localization-dependent translation requires a functional interaction between the 5' and 3' ends of oskar mRNA.

Authors:  N Gunkel; T Yano; F H Markussen; L C Olsen; A Ephrussi
Journal:  Genes Dev       Date:  1998-06-01       Impact factor: 11.361

10.  Genetic interactions of Drosophila melanogaster arrest reveal roles for translational repressor Bruno in accumulation of Gurken and activity of Delta.

Authors:  Nan Yan; Paul M Macdonald
Journal:  Genetics       Date:  2004-11       Impact factor: 4.562

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