Localized XId3 mRNA activation in Xenopus embryos by cytoplasmic polyadenylation

Mechanisms of Development

Volumn 88, Issue 1, 1999, Pages 15-31

  Afouda, Anatole B ^a   Reynaud Deonauth, Sorogini ^a   Mohun, Tim ^b   Spohr, Georges ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

^b NATIONAL INSTITUTE FOR MEDICAL RESEARCH   (United Kingdom)

Author keywords

3' UTR translation; Animal cap; Control prepattern axis; Cytoplasmic polyadenylation; Embryo; Epithelial sensorial layer; Galactosidase; Gasrtrula; GVBD; HLH bHLH transcription factor; Id2 sequence; Id3; In situ; Inhibition; Localization; Maternal mRNA; Oocyte maturation; Palindrome CPE; Post transcriptional regulation; Xenopus development

Indexed keywords

MESSENGER RNA;

ARTICLE; EMBRYO DEVELOPMENT; NONHUMAN; OOCYTE; OOCYTE MATURATION; POLYADENYLATION; PRIORITY JOURNAL; TRANSCRIPTION REGULATION; XENOPUS;

3' UNTRANSLATED REGIONS; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BLASTOCYST; CYTOPLASM; DNA-BINDING PROTEINS; EMBRYO, NONMAMMALIAN; FEMALE; GASTRULA; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IN SITU HYBRIDIZATION; INHIBITOR OF DIFFERENTIATION PROTEIN 2; INHIBITOR OF DIFFERENTIATION PROTEINS; MOLECULAR SEQUENCE DATA; NEOPLASM PROTEINS; OOCYTES; REGULATORY SEQUENCES, NUCLEIC ACID; REPRESSOR PROTEINS; RNA, MESSENGER; TRANSCRIPTION FACTORS; XENOPUS;

ANIMALIA; VERTEBRATA;

EID: 0032858993     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4773(99)00166-5     Document Type: Article

References (42)

1. Bachvarova R.F. A maternal tail of poly(A): the long and the short of it. Cell. 69:1992;895-897.
2. Ballantyne S., Daniel D.L. Jr, Wickens M. A dependent pathway of cytoplasmic polyadenylation reactions linked to cell cycle control by c-mos and CDK1 activation. Mol. Biol. Cell. 8:1997;1633-1648.
3. Barkoff A., Ballantyne S., Wickens M. Meiotic maturation in Xenopus requires polyadenylation of multiple mRNAs. EMBO J. 17:1998;3168-3175.
4. Benezra R., Davis R.L., Lockshon D., Turner D.L., Weintraub H. The protein Id: a negative regulator of Helix-Loop-Helix DNA binding proteins. Cell. 61:1990;49-59.
5. Christy B.A., Sanders L.K., Lau L.F., Copeland N.G., Jemkins N.A., Nathans D. An Id-related helix-loop-helix protein encoded by a growth factor-inducible gene. Proc. Natl. Acad. Sci. USA. 88:1991;1815-1819.
6. Curtis D., Lehmann R., Zamore P.D. Translational regulation in development. Cell. 81:1995;171-178.
7. de Wet J.R., Wood K.V., DeLuca M., Helinski D.R., Subramani S. Firefly luciferase gene: structure and expression in mammalian cells. Mol. Cell. Biol. 7:1987;725-737.
8. Deed R.W., Bianchi S.M., Atherton G.T., Johnston D., Santibanez-Koref M., Murphy J.J., Norton J.D. An immediate early human gene encodes an Id-like helix-loop-helix protein and is regulated by protein kinase C activation in diverse cell types. Oncogene. 8:1993;599-607.
9. Etkin L.D., Maxson R.E. Jr. The synthesis of authentic sea urchin transcriptional and translational products by sea urchin histone genes injected into Xenopus laevis oocytes. Dev. Biol. 75:1980;13-25.
10. Gerhart J., Danilchik M., Doniach T., Roberts S., Rowning B., Stewart R. Cortical rotation of the Xenopus egg: consequences for the anteroposterior pattern of embryonic dorsal development. Development. 107:1989;37-51.
11. Gurdon G.B., Wakefield L. Microinjection of amphibian oocytes and eggs for the analysis of transcription. Microinjection and Organelles Transplantation Techniques. 1986;269-299 Academic Press, London.
12. Hake L.E., Richter J.D. Translational regulation of maternal mRNA. Biochim. Biophys. Acta. 1332:1997;M31-M38.
13. Harland R.M. In situ hybridization: an improved whole-mount method for Xenopus embryos. Methods Cell Biol. 36:1991;685-695.
14. Hausen P., Riebesell M. The early development of Xenopus laevis. An Atlas of Histology, Verlag für Naturfolschung. 1991;Springer, Berlin.
15. Huarte J., Belin D., Vassalli A., Strickland S., Vassalli J.D. Meiotic maturation of mouse oocytes triggers the translation and polyadenylation of dormant tissue-type plasminogen activator mRNA. Genes Dev. 1:1987;1201-1211.
16. Jackson R.J. Cytoplasmic regulation of mRNA function: the importance of the 3′ untranslated region. Cell. 74:1993;9-14.
17. Johnson J.E., Birren S.J., Anderson D.J. Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors. Nature. 346:1990;858-861.
18. Keller R.E. The cellular basis of gastrulation in Xenopus laevis: active postinvolution convergence and extension by mediolateral interdigitation. Amer. Zool. 24:1984;586-603.
19. Laimins L.A., Khoury G., Gorman C., Howard B., Gruss P. Host-specific activation of transcription by tandem repeats from simian virus 40 and Moloney murine sarcoma virus. Proc. Natl. Acad. Sci. USA. 79:1982;6453-6457.
20. Latinkic B.V., Umbhauer M., Neal K.A., Lerchner W., Smith J.C., Cunliffe V. The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins. Genes Dev. 11:1997;3265-3276.
21. Lo L.C., Johnson J.E., Wuenschell C.W., Saito T., Anderson D.J. Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells. Genes Dev. 5:1991;1524-1537.
22. McGrew L.L., Richter J.D. Translational control by cytoplasmic polyadenylation during Xenopus oocyte maturation: characterization of cis and trans elements and regulation by cyclin/MPF. EMBO J. 9:1990;3743-3751.
23. Modak S.P., Principaud E., Spohr G. Regulation of Xenopus c-myc promoter activity in oocytes and embryos. Oncogene. 8:1993;645-654.
24. Piko L., Clegg K.B. Quantitative changes in total RNA, total poly(A), and ribosomes in early mouse embryos. Dev. Biol. 89:1982;362-378.
25. Rescan P.Y. Identification in a fish species of two Id (inhibitor of DNA binding/differentiation)-related helix-loop-helix factors expressed in the slow oxidative muscle fibers. Eur. J. Biochem. 247:1997;870-876.
26. Richter J.D. Translational control during early development. BioEssays. 13:1991;179-183.
27. Salles F.J., Strickland S. Rapid and sensitive analysis of mRNA polyadenylation states by PCR. PCR Methods Appl. 4:1995;317-321.
28. 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.
29. Simon R., Tassan J.P., Richter J.D. Translational control by poly(A) elongation during Xenopus development: differential repression and enhancement by a novel cytoplasmic polyadenylation element. Genes Dev. 6:1992;2580-2591.
30. Simon R., Wu L., Richter J.D. Cytoplasmic polyadenylation of activin receptor mRNA and the control of pattern formation in Xenopus development. Dev. Biol. 179:1996;239-250.
31. Sleigh M.J. A nonchromatographic assay for expression of the chloramphenicol acetyltransferase gene in eucaryotic cells. Anal. Biochem. 156:1986;251-256.
32. Smith W.C., Harland R.M. Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center. Cell. 67:1991;753-765.
33. Smith W.C., Harland R.M. Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos. Cell. 70:1992;829-840.
34. Stebbins-Boaz B., Richter J.D. Multiple sequence elements and a maternal mRNA product control cdk2 RNA polyadenylation and translation during early Xenopus development. Mol. Cell. Biol. 14:1994;5870-5880.
35. Stumpf G., Goppelt A., Domdey H. Pre-mRNA topology is important for 3′-end formation in Saccharomyces cerevisiae and mammals. Mol. Cell. Biol. 16:1996;2204-2213.
36. Stutz A., Conne B., Huarte J., Gubler P., Volkel V., Flandin P., Vassalli J.D. Masking, unmasking, and regulated polyadenylation cooperate in the translational control of a dormant mRNA in mouse oocytes. Genes Dev. 12:1998;2535-2548.
37. Sun X.H., Copeland N.G., Jenkins N.A., Baltimore D. Id proteins Id1 and Id2 selectively inhibit DNA binding by one class of helix-loop-helix proteins. Mol. Cell. Biol. 11:1991;5603-5611.
38. Vize P.D., Melton D.A., Hemmati-Brivanlou A., Harland R.M. Assays for gene function in developing Xenopus embryos. Methods Cell Biol. 36:1991;367-387.
39. Weintraub H., Davis R., Tapscott S., Thayer M., Krause M., Benezra R., Blackwell K.T., Turner D., Rupp R., Hollenberg S., Zhuang Y., Lassar A. The myoD gene family: nodal point during specification of the muscle cell lineage. Science. 251:1991;761-766.
40. Wilson R., Mohun T. XIdx, a dominant negative regulator of bHLH function in early Xenopus embryos. Mech. Dev. 49:1995;211-222.
41. Yisraeli J.K., Melton D.A. Synthesis of long, capped transcripts in vitro by SP6 and T7 RNA polymerases. Methods Enzymol. 180:1989;42-50.
42. Zhang H., Reynaud S., Kloc M., Etkin L.D., Spohr G. Id gene activity during Xenopus embryogenesis. Mech. Dev. 50:1995;119-130.