In vitro translation extracts prepared from Drosophila ovaries and embryos

Biochemical and Biophysical Research Communications

Volumn 270, Issue 2, 2000, Pages 473-481

  Lie, Yung S ^a   MacDonald, Paul M ^a,b  

^a STANFORD UNIVERSITY   (United States)

^b UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA;

ARTICLE; DEVELOPMENT; DROSOPHILA; EMBRYO; FEMALE; NONHUMAN; OVARY; PRIORITY JOURNAL; TRANSLATION REGULATION;

ANIMALIA; DROSOPHILA;

EID: 0034643285     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2000.2453     Document Type: Article

References (32)

1. Davidson E. H. Gene Activity in Early Development. 1986;Academic Press, Inc. Orlando.
2. Grainger J. L., Winkler M. M., Shen S. S., Steinhardt R. A. Intracellular pH controls protein synthesis rate in the sea urchine egg and early embryo. Dev. Biol. 68:1979;396-406.
3. Curtis D., Lehmann R., Zamore P. D. Translational regulation in development. Cell. 81:1995;171-178.
4. Macdonald P. M., Smibert C. A. Translational regulation of maternal mRNAs. Curr. Opin. Genet. Dev. 6:1996;403-407.
5. St. Johnston D. The intracellular localization of messenger RNAs. Cell. 81:1995;161-170.
6. Wickens M., Kimble J., Strickland S. Translational control of developmental decisions. Hershey J. W. B., Mathews M. B., Sonenberg N. Translational Control. 1996;411-450 Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
7. Wharton R. P., Struhl G. RNA regulatory elements mediate control of Drosophila body pattern by the posterior morphogen nanos. Cell. 67:1991;955-967.
8. Kim-Ha J., Kerr K., Macdonald P. M. Translational regulation of oskar mRNA by bruno, an ovarian RNA-binding protein, is essential. Cell. 81:1995;403-412.
9. Smibert C. A., Wilson J. E., Kerr K., Macdonald P. M. smaug protein represses translation of unlocalized nanos mRNA in the Drosophila embryo. Genes & Dev. 10:1996;2600-2609.
10. Gebauer Ft., Xu W., Cooper G. M., Richter J. D. Translational control by cytoplasmic polyadenylation of c-mos mRNA is necessary for oocyte maturation in the mouse. EMBO J. 13:1994;5712-5720.
11. Sheets M. D., Wu M., Wickens M. Polyadenylation of c-mos mRNA as a control point in Xenopus meiotic maturation. Nature. 374:1995;511-516.
12. Richter J. D. Dynamics of poly(A) addition and removal during development. Hershey J. W. B., Mathews M. B., Sonenberg N. Translational Control. 1996;481-504 Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
13. Sallés F. J., Lieberfarb M. E., Wreden C., Gergen J. P., Strickland S. Coordinate initiation of Drosophila development by regulated polyadenylation of maternal messenger RNAs. Science. 266:1994;1996-1999.
14. Kuge H., Richter J. D. Cytoplasmic 3′ poly(A) addition induces 5′ cap ribose methylation: implications for translational control of maternal mRNA. EMBO J. 14:1995;6301-6210.
15. Tarun S. Z., Sachs A. B. Association of the yeast poly(A) tail binding protein with translation initation factor elF-4G. EMBO J. 15:1996;7168-7177.
16. Sachs A. B., Sarnow P., Hentze M. W. Starting at the beginning, middle, and end: Translation initiation in eukaryotes. Cell. 89:1997;831-838.
17. Ostareck D. H., Ostareck-Lederer A., Wilm M., Thiele B. J., Mann M., Hentze M. W. mRNA silencing in erythroid differentiation: hnRNP K and hnRNP E1 regulate 15-lipoxygenase translation from the 3′ end. Cell. 89:1997;597-606.
18. Webster P. J., Liang L., Berg C. A., Lasko P., Macdonald P. M. Translational repressor bruno plays multiple roles in development and is widely conserved. Genes Dev. 11:1997;2510-2521.
19. Lie Y., Macdonald P. M. Translational regulation of oskar mRNA occurs independent of the cap and poly(A) tail in Drosophila ovarian extracts. Development. 126:1999;4989-4996.
20. Smibert C. A., Lie Y. S., Shillinglaw W., Henzel W. J., Macdonald P. M. Smaug, a novel and conserved protein, contributes to repression of nanos mRNA translation in vitro. RNA. 5:1999;1535-1547.
21. Sampson J. R., Saks M. E. Contributions of discrete tRNA(Ser) domains to aminoacylation by E. coli seryl-tRNA synthetase: A kinetic analysis using model RNA substrates. Nucleic Acids Res. 21:1993;4467-4475.
22. Tarun S. Z. Jr., Sachs A. B. A common function for mRNA 5′ and 3′ ends in translation initiation in yeast. Genes Dev. 9:1995;2997-3007.
23. McBratney S., Sarnow P. Evidence for involvement of trans-acting factors in selection of the AUG start codon during eukaryotic translational initiation. Mol. Cell Biol. 16:1996;3523-3534.
24. Shaffer C. D., Wuller J. M., Elgin S. C. Raising large quantities of Drosophila for biochemical experiments. Methods Cell Biol. 44:1994;99-108.
25. Iizuka N., Najita L., Franzusoff A., Sarnow P. Cap-dependent and cap-independent translation by internal initiation of mRNAs in cell extracts prepared from Saccharomyces cerevisiae. Mol. Cell Biol. 14:1994;7322-7330.
26. Beelman C. A., Parker R. Degradation of mRNA in eukaryotes. Cell. 81:1995;179-183.
27. Jacobson A. Poly(A) metabolism and translation: The closed-loop model. Hershey J. W. B., Mathews M. B., Sonenberg N. Translational Control. 1996;451-480 Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
28. Sonenberg N. mRNA 5′ Cap-binding protein elF4E and control of cell growth. Hershey J. W. B., Mathews M. B., Sonenberg N. Translational Control. 1996;245-269 Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
29. Wu L., Wells D., Tay J., Mendis D., Abbott M. A., Barnitt A., Quinlan E., Heynen A., Fallon J. R., Richter J. D. CPEB-mediated cytoplasmic polyadenylation and the regulation of experience-dependent translation of alpha-CaMKII mRNA at synapses. Neuron. 21:1998;1129-1139.
30. Gebauer F., Corona D. F., Preiss T., Becker P. B., Hentze M. W. Translational control of dosage compensation in Drosophila by Sex-lethal: cooperative silencing via the 5′ and 3′ UTRs of msl-2 mRNA is independent of the poly(A) tail. EMBO J. 18:1999;6146-6154.
31. Castagnetti S., Hentze M. W., Ephrussi A., Gebauer F. Control of oskar mRNA translation by Bruno in a novel cell-free system from Drosophila ovaries. Development. 127:2000;1063-1068.
32. Wreden C., Verrotti A. C., Schisa J. A., Lieberfarb M. E., Strickland S. Nanos and pumilio establish embryonic polarity in Drosophila by promoting posterior deadenylation of hunchback mRNA. Development. 124:1997;3015-3023.