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JOURNAL ARTICLES
A conserved 90 nucleotide element mediates translational repression of nanos RNA
E.R. Gavis, L. Lunsford, S.E. Bergsten, R. Lehmann
Development 1996 122: 2791-2800;
E.R. Gavis
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L. Lunsford
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S.E. Bergsten
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R. Lehmann
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Summary

Correct formation of the Drosophila body plan requires restriction of nanos activity to the posterior of the embryo. Spatial regulation of nanos is achieved by a combination of RNA localization and localization-dependent translation such that only posteriorly localized nanos RNA is translated. Cis-acting sequences that mediate both RNA localization and translational regulation lie within the nanos 3′ untranslated region. We have identified a discrete translational control element within the nanos 3′ untranslated region that acts independently of the localization signal to mediate translational repression of unlocalized nanos RNA. Both the translational regulatory function of the nanos 3′UTR and the sequence of the translational control element are conserved between D. melanogaster and D. virilis. Furthermore, we show that the RNA helicase Vasa, which is required for nanos RNA localization, also plays a critical role in promoting nanos translation. Our results specifically exclude models for translational regulation of nanos that rely on changes in polyadenylation.

Reference

    1. Barker D. D.,
    2. Wang C.,
    3. Moore J.,
    4. Dickinson L. K.,
    5. Lehmann R.
    (1992) Pumilio is essential for function but not for distribution of the Drosophila abdominal determinant Nanos. Genes Dev 6, 2312–2326
    OpenUrlAbstract/FREE Full Text
    1. Blake M. S.,
    2. Johnston K. H.,
    3. Russell-Jones G. J.,
    4. Gotschlich E. C.
    (1984) A rapid, sensitive method for detection of alkaline phosphatase conjugated anti-antibody on Western blots. Analyt. Bioch 136, 175–179
    OpenUrlCrossRefPubMedWeb of Science
    1. Curtis D.,
    2. Apfeld J.,
    3. Lehmann R.
    (1995) nanos is an evolutionarily conserved organizer of anterior-posterior polarity. Development 121, 1899–1910
    OpenUrlAbstract
    1. Curtis D.,
    2. Lehmann R.,
    3. Zamore P. D.
    (1995) Translational regulation in development. Cell 81, 171–178
    OpenUrlCrossRefPubMedWeb of Science
    1. Driever W.,
    2. Nusslein-Volhard C.
    (1988) The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner. Cell 54, 95–104
    OpenUrlCrossRefPubMedWeb of Science
    1. Driever W.,
    2. Nusslein-Volhard C.
    (1988) A gradient of bicoid protein in Drosophila embryos. Cell 54, 83–93
    OpenUrlCrossRefPubMedWeb of Science
    1. Driever W.,
    2. Thoma G.,
    3. Nusslein-Volhard C.
    (1989) Determination of spatial domains of zygotic gene expression in the Drosophila embryo by the affinity of binding sites for the bicoid morphogen. Nature 340, 363–367
    OpenUrlCrossRefPubMed
    1. Dubnau J.,
    2. Struhl G.
    (1996) RNA recognition and translational regulation by a homeodomain protein. Nature 379, 694–699
    OpenUrlCrossRefPubMed
    1. Ephrussi A.,
    2. Dickinson L. K.,
    3. Lehmann R.
    (1991) oskar organizes the germ plasm and directs localization of the posterior determinant nano s. Cell 66, 37–50
    OpenUrlCrossRefPubMedWeb of Science
    1. Ephrussi A.,
    2. Lehmann R.
    (1992) Induction of germ cell formation by oskar. Nature 358, 387–392
    OpenUrlCrossRefPubMedWeb of Science
    1. Evans T. C.,
    2. Crittenden S. L.,
    3. Kodoyianni V.,
    4. Kimble J.
    (1994) Translational control of maternal glp-1 mRNA establishes an asymmetry in the C. elegans embryo. Cell 77, 183–194
    OpenUrlCrossRefPubMedWeb of Science
    1. Gavis E. R.,
    2. Curtis D.,
    3. Lehmann R.
    (1996) Identification of cis -acting sequences that control nanos RNA localization. Dev. Biol 176, 36–50
    OpenUrlCrossRefPubMedWeb of Science
    1. Gavis E. R.,
    2. Lehmann R.
    (1992) Localization of nano s RNA controls embryonic polarity. Cell 71, 301–313
    OpenUrlCrossRefPubMedWeb of Science
    1. Gavis E. R.,
    2. Lehmann R.
    (1994) Translational regulation of nanos by RNA localization. Nature 369, 315–318
    OpenUrlCrossRefPubMed
    1. Hay B.,
    2. Ackerman L.,
    3. Barbel S.,
    4. Jan L. Y.,
    5. Jan Y. N.
    (1988) Identification of a component of Drosophila polar granules. Development 103, 625–640
    OpenUrlAbstract/FREE Full Text
    1. Hay B.,
    2. Jan L. Y.,
    3. Jan Y. N.
    (1988) A protein component of Drosophila polar granules is encoded by vasa and has extensive sequence similarity to ATP-dependent helicases. Cell 55, 577–587
    OpenUrlCrossRefPubMedWeb of Science
    1. Hulskamp M.,
    2. Tautz D.
    (1991) Gap genes and gradients- the logic behind the gaps. BioEssays 13, 261–268
    OpenUrlCrossRefPubMed
    1. Jaeger J.A.,
    2. Turner D.H.,
    3. Zuker M.
    (1989) Improved predictions of secondary structures for RNA. Proc. Natl. Acad. Sci. USA 86, 7706–7710
    OpenUrlAbstract/FREE Full Text
    1. Jaeger J.A.,
    2. Turner D.H.,
    3. Zuker M.
    (1989) Predicting optimal and suboptimal secondary structures for RNA. Methods Enzymol 183, 281–306
    OpenUrlWeb of Science
    1. Kim-Ha J.,
    2. Kerr K.,
    3. Macdonald P. M.
    (1995) Translational regulation of oskar mRNA by Bruno, an ovarian RNA-binding protein is essential. Cell 81, 403–412
    OpenUrlCrossRefPubMedWeb of Science
    1. Kim-Ha J.,
    2. Smith J. L.,
    3. Macdonald P. M.
    (1991) oskar mRNA is localized to the posterior pole of the Drosophila oocyte. Cell 66, 23–35
    OpenUrlCrossRefPubMedWeb of Science
    1. Lasko P. F.,
    2. Ashburner M.
    (1990) Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development. Genes Dev 4, 905–921
    OpenUrlAbstract/FREE Full Text
    1. Lasko P. F.,
    2. Ashburner M.
    (1988) The product of the Drosophila gene vasa is very similar to eukaryotic initiation factor-4A. Nature 335, 611–617
    OpenUrlCrossRefPubMedWeb of Science
    1. Lehmann R.,
    2. Nusslein-Volhard C.
    (1991) The maternal gene nanos has a central role in posterior pattern formation of the Drosophila embryo. Development 112, 679–691
    OpenUrlAbstract
    1. Liang L.,
    2. Diehl-Jones W.,
    3. Lasko P.
    (1994) Localization of vasa protein to the Drosophila pole plasm is independent of its RNA-binding and helicase activities. Development 120, 1201–1211
    OpenUrlAbstract
    1. Markussen F.-H.,
    2. Michon A.-M.,
    3. Breitwieser W.,
    4. Ephrussi A.
    (1995) Translational control of oskar generates Short OSK, the isoform that induces pole plasm assembly. Development 121, 3723–3732
    OpenUrlAbstract
    1. Mismer D.,
    2. Rubin G. M.
    (1987) Analysis of the promoter of the nina E opsin gene in Drosophila melanogaster. Genetics 116, 565–578
    OpenUrlAbstract/FREE Full Text
    1. Murata Y.,
    2. Wharton R. P.
    (1995) Binding of Pumilio to maternal hunchback mRNA is required for posterior patterning in Drosophila embryos. Cell 80, 747–756
    OpenUrlCrossRefPubMedWeb of Science
    1. Rivera-Pomar R.,
    2. Niessing D.,
    3. Schmidt-Ott U.,
    4. Gehring W. J.,
    5. Jäckle H.
    (1996) RNA binding and translational suppression by bicoid. Nature 379, 746–749
    OpenUrlCrossRefPubMed
    1. Rongo C.,
    2. Gavis E. R.,
    3. Lehmann R.
    (1995) Localization of oskar RNA regulates oskar translation and requires Oskar protein. Development 121, 2737–2746
    OpenUrlAbstract
    1. Sachs A. B.,
    2. Davis R. W.
    (1989) The poly(A)-binding protein is requiredfor poly(A) shortening and 60S ribosomal subunit-dependent translational initiation. Cell 58, 857–867
    OpenUrlCrossRefPubMedWeb of Science
    1. Salles F. J.,
    2. Lieberfarb M. E.,
    3. Wreden C.,
    4. Gergen J. P.,
    5. Strickland S.
    (1994) Coordinate initiation of Drosophila development by regulated polyadenylation of maternal mRNAs. Science 266, 1996–1999
    OpenUrlAbstract/FREE Full Text
    1. Salles F. J.,
    2. Strickland S.
    (1995) Rapid and sensitive analysis of mRNA polyadenylation states by PCR. PCR Methods Applications 4, 317–321
    OpenUrlCrossRefPubMedWeb of Science
    1. Schmid H.-P.,
    2. Schönfelder M.,
    3. Setyono B.,
    4. Köhler K.
    (1983) 76-kDa poly(A)-binding protein is involved in the formation of 48S initiation complexes. FEBS Letters 157, 105–109
    OpenUrlCrossRefPubMed
    1. Sieliwanowicz B.
    (1987) The influence of poly(A)-binding proteins on translation of poly(A)+ RNA in a cell-free system from embryo axes of dry pea seeds. Biochim. Biophys. Acta 908, 54–59
    OpenUrl
    1. St Johnston D.
    (1995) The intracellular localization of messenger RNAs. Cell 81, 161–170
    OpenUrlCrossRefPubMedWeb of Science
    1. Struhl G.,
    2. Struhl K.,
    3. Macdonald P. M.
    (1989) The gradient morphogen bicoid is a concentration-dependent transcriptional activator. Cell 57, 1259–1273
    OpenUrlCrossRefPubMedWeb of Science
    1. Tarun S. Z., Jr.,
    2. Sachs A. B.
    (1995) A common function for mRNA 5and 3 ends in translation initiation in yeast. Genes Dev 9, 2997–3007
    OpenUrlAbstract/FREE Full Text
    1. Vassalli J.-D.,
    2. Stutz A.
    (1995) Awakening dormant RNAs. Curr. Biol 5, 476–479
    OpenUrlCrossRefPubMedWeb of Science
    1. Wang C.,
    2. Lehmann R.
    (1991) Nanos is the localized posterior determinant in Drosophila. Cell 66, 637–647
    OpenUrlCrossRefPubMedWeb of Science
    1. Wharton R. P.,
    2. Struhl G.
    (1989) Structure of the Drosophila BicaudalD protein and its role in localizing the posterior determinant nanos. Cell 59, 881–892
    OpenUrlCrossRefPubMedWeb of Science
    1. Zuker M.
    (1989) On finding all suboptimal foldings of an RNA molecule. Science 244, 48–52
    OpenUrlAbstract/FREE Full Text
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JOURNAL ARTICLES
A conserved 90 nucleotide element mediates translational repression of nanos RNA
E.R. Gavis, L. Lunsford, S.E. Bergsten, R. Lehmann
Development 1996 122: 2791-2800;
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JOURNAL ARTICLES
A conserved 90 nucleotide element mediates translational repression of nanos RNA
E.R. Gavis, L. Lunsford, S.E. Bergsten, R. Lehmann
Development 1996 122: 2791-2800;

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