Bruno negatively regulates germ cell-less expression in a BRE-independent manner

Mechanisms of Development

Volumn 126, Issue 7, 2009, Pages 503-516

  Moore, Jocelyn ^a   Han, Hong ^a   Lasko, Paul ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

Bruno; Drosophila; Germ cell less; Germline; Oogenesis; Regulation; RNA binding; Translation

Indexed keywords

MEMBRANE PROTEIN; MESSENGER RNA; PROTEIN BRU; PROTEIN GCL; UNCLASSIFIED DRUG;

3' UNTRANSLATED REGION; ARTICLE; DROSOPHILA; GERM CELL; IN VITRO STUDY; NONHUMAN; OOCYTE DEVELOPMENT; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN EXPRESSION; TRANSLATION REGULATION;

3' UNTRANSLATED REGIONS; ANIMALS; ANIMALS, GENETICALLY MODIFIED; BASE SEQUENCE; DNA-BINDING PROTEINS; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; EMBRYO, NONMAMMALIAN; EMBRYONIC DEVELOPMENT; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; OOCYTES; OOGENESIS; PROTEIN BINDING; PROTEIN BIOSYNTHESIS; RECOMBINANT PROTEINS; REPRESSOR PROTEINS; RESPONSE ELEMENTS; RNA, MESSENGER; RNA-BINDING PROTEINS;

EID: 67349197572     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mod.2009.04.002     Document Type: Article

References (44)

1. Brand A.H., and Perrimon N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118 (1993) 401-415
2. Chekulaeva M., Hentze M.W., and Ephrussi A. Bruno acts as a dual repressor of oskar translation, promoting mRNA oligomerization and formation of silencing particles. Cell 124 (2006) 521-533
3. Delaunay J., Le Mee G., Ezzeddine N., Labesse G., Terzian C., Capri M., and Ait-Ahmed O. The Drosophila Bruno paralogue Bru-3 specifically binds the EDEN translational repression element. Nucleic Acids Res. 32 (2004) 3070-3082
4. Deo R.C., Bonanno J.B., Sonenberg N., and Burley S.K. Recognition of polyadenylate RNA by the poly(A)-binding protein. Cell 98 (1999) 835-845
5. Drosophila 12 Genomes Consortium. Evolution of genes and genomes on the Drosophila phylogeny. Nature 450 (2007) 203-218
6. Filardo P., and Ephrussi A. Bruno regulates gurken during Drosophila oogenesis. Mech. Dev. 120 (2003) 289-297
7. Findley S.D., Tamanaha M., Clegg N.J., and Ruohola-Baker H. Maelstrom, a Drosophila spindle-class gene, encodes a protein that colocalizes with Vasa and RDE1/AGO1 homolog, Aubergine, in nuage. Development 130 (2003) 859-871
8. Forrest K.M., and Gavis E.R. Live imaging of endogenous RNA reveals a diffusion and entrapment mechanism for nanos mRNA localization in Drosophila. Curr. Biol. 13 (2003) 1159-1168
9. Gerber A.P., Luschnig S., Krasnow M.A., Brown P.O., and Herschlag D. Genome-wide identification of mRNAs associated with the translational regulator PUMILIO in Drosophila melanogaster. Proc. Natl. Acad. Sci. USA 103 (2006) 4487-4492
10. Good P.J., Chen Q., Warner S.J., and Herring D.C. A family of human RNA-binding proteins related to the Drosophila Bruno translational regulator. J. Biol. Chem. 275 (2000) 28583-28592
11. Handa N., Nureki O., Kurimoto K., Kim I., Sakamoto H., Shimura Y., Muto Y., and Yokoyama S. Structural basis for recognition of the tra mRNA precursor by the Sex-lethal protein. Nature 398 (1999) 579-585
12. Jongens T.A., Ackerman L.D., Swedlow J.R., Jan L.Y., and Jan Y.N. Germ cell-less encodes a cell type-specific nuclear pore-associated protein and functions early in the germ-cell specification pathway of Drosophila. Genes Dev. 8 (1994) 2123-2136
13. Jongens T.A., Hay B., Jan L.Y., and Jan Y.N. The germ cell-less gene product: a posteriorly localized component necessary for germ cell development in Drosophila. Cell 70 (1992) 569-584
14. Kim-Ha J., Kerr K., and Macdonald P.M. Translational regulation of oskar mRNA by bruno, an ovarian RNA-binding protein, is essential. Cell 81 (1995) 403-412
15. King R.C. Ovarian Development in Drosophila melanogaster (1970), Academic Press, New York
16. Kobayashi S., Amikura R., Nakamura A., and Lasko P.F. Techniques for analyzing protein and RNA distribution in Drosophila ovaries and embryos at structural and ultrastructural resolution. In: Richter J. (Ed). Advances in Molecular Biology: A Comparative Methods Approach to the Study of Oocytes and Embryos (1999), Oxford University Press, Oxford 426-445
17. Larkin M.A., Blackshields G., Brown N.P., Chenna R., McGettigan P.A., McWilliam H., Valentin F., Wallace I.M., Wilm A., Lopez R., Thompson J.D., Gibson T.J., and Higgins D.G. Clustal W and Clustal X version 2.0. Bioinformatics 23 (2007) 2947-2948
18. Lasko P.F., and Ashburner M. Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development. Genes Dev. 4 (1990) 905-921
19. Leatherman J.L., Levin L., Boero J., and Jongens T.A. Germ cell-less acts to repress transcription during the establishment of the Drosophila germ cell lineage. Curr. Biol. 12 (2002) 1681-1685
20. Lehmann R., and Nüsslein-Volhard C. Abdominal segmentation, pole cell formation, and embryonic polarity require the localized activity of oskar, a maternal gene in Drosophila. Cell 47 (1986) 141-152
21. Lehmann R., and Nüsslein-Volhard C. The maternal gene nanos has a central role in posterior pattern formation of the Drosophila embryo. Development 112 (1991) 679-691
22. Lunde B.M., Moore C., and Varani G. RNA-binding proteins: modular design for efficient function. Nat. Rev. Mol. Cell. Biol. 8 (2007) 479-490
23. Nakamura A., Amikura R., Hanyu K., and Kobayashi S. Me31B silences translation of oocyte-localizing RNAs through the formation of cytoplasmic RNP complex during Drosophila oogenesis. Development 128 (2001) 3233-3242
24. Nakamura A., Sato K., and Hanyu-Nakamura K. Drosophila cup is an eIF4E binding protein that associates with Bruno and regulates oskar mRNA translation in oogenesis. Dev. Cell 6 (2004) 69-78
25. Oberstrass F.C., Auweter S.D., Erat M., Hargous Y., Henning A., Wenter P., Reymond L., Amir-Ahmady B., Pitsch S., Black D.L., and Allain F.H.T. Structure of PTB bound to RNA: specific binding and implications for splicing regulation. Science 309 (2005) 2054-2057
26. Parisi M.J., Deng W., Wang Z., and Lin H. The arrest gene is required for germline cyst formation during Drosophila oogenesis. Genesis 29 (2001) 196-209
27. Robertson S.E., Dockendorff T.C., Leatherman J.L., Faulkner D.L., and Jongens T.A. Germ cell-less is required only during the establishment of the germ cell lineage of Drosophila and has activities which are dependent and independent of its localization to the nuclear envelope. Dev. Biol. 215 (1999) 288-297
28. Schüpbach T., and Wieschaus E. Germline autonomy of maternal-effect mutations altering the embryonic body pattern of Drosophila. Dev. Biol. 113 (1986) 443-448
29. Schüpbach T., and Wieschaus E. Female sterile mutations on the second chromosome of Drosophila melanogaster. II. Mutations blocking oogenesis or altering egg morphology. Genetics 129 (1991) 1119-1136
30. Snee M., Benz D., Jen J., and Macdonald P.M. Two distinct domains of Bruno bind specifically to the oskar mRNA. RNA Biol. 5 (2008) 1-9
31. Snee M.J., Harrison D., Yan N., and Macdonald P.M. A late phase of Oskar accumulation is crucial for posterior patterning of the Drosophila embryo, and is blocked by ectopic expression of Bruno. Differentiation 75 (2007) 246-255
32. Sugimura I., and Lilly M.A. Bruno inhibits the expression of mitotic cyclins during the prophase I meiotic arrest of Drosophila oocytes. Dev. Cell 10 (2006) 127-135
33. Suzuki H., Jin Y., Otani H., Yasuda K., and Inoue K. Regulation of alternative splicing of alpha-actinin transcript by Bruno-like proteins. Genes Cells 7 (2002) 133-141
34. Thomson T., and Lasko P. Drosophila tudor is essential for polar granule assembly and pole cell specification, but not for posterior patterning. Genesis 40 (2004) 164-170
35. Van Doren M., Williamson A.L., and Lehmann R. Regulation of zygotic gene expression in Drosophila primordial germ cells. Curr. Biol. 8 (1998) 243-246
36. Vardy L., and Orr-Weaver T.L. Regulating translation of maternal messages: multiple repression mechanisms. Trends Cell Biol. 17 (2007) 547-554
37. Wang X., and Tanaka Hall T.M. Structural basis for recognition of AU-rich element RNA by the HuD protein. Nat. Struct. Mol. Biol. 8 (2001) 141-145
38. Wang Z., and Lin H. Sex-lethal is a target of Bruno-mediated translational repression in promoting the differentiation of stem cell progeny during Drosophila oogenesis. Dev. Biol. 302 (2007) 160-168
39. Webster P.J., Liang L., Berg C.A., Lasko P., and Macdonald P.M. Translational repressor bruno plays multiple roles in development and is widely conserved. Genes Dev. 11 (1997) 2510-2521
40. Weigel D., Jurgens G., Klingler M., and Jackle H. Two gap genes mediate maternal terminal pattern information in Drosophila. Science 248 (1990) 495-498
41. Wilhelm J.E., and Smibert C.A. Mechanisms of translational regulation in Drosophila. Biol. Cell 97 (2005) 235-252
42. Wilson R.J., Goodman J.L., Strelets V.B., the FlyBase consortium,. FlyBase: integration and improvements to query tools. Nucleic Acids Res. 36 (2008) D588-D593
43. Zamore P.D., Bartel D.P., Lehmann R., and Williamson J.R. The Pumilio-RNA interaction: A single RNA-binding domain monomer recognizes a bipartite target sequence. Biochemistry 38 (1999) 596-604
44. Zimyanin V.L., Belaya K., Pecreaux J., Gilchrist M.J., Clark A., Davis I., and St Johnston D. In vivo imaging of oskar mRNA transport reveals the mechanism of posterior localization. Cell 134 (2008) 843-853