Xenopus Embryonic Poly(A) Binding Protein 2 (ePABP2) Defines a New Family of Cytoplasmic Poly(A) Binding Proteins Expressed during the Early Stages of Vertebrate Development

Genesis (United States)

Volumn 38, Issue 4, 2004, Pages 166-175

  Good, Peter J ^a,c   Abler, Lisa ^b   Herring, Dina ^a   Sheets, Michael D ^b  

^a LOUISIANA STATE UNIVERSITY HEALTH SCIENCES CENTER   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

RNA binding protein; Vertebrate; Xenopus

Indexed keywords

COMPLEMENTARY DNA; CYTOPLASM PROTEIN; MESSENGER RNA; POLYADENYLIC ACID BINDING PROTEIN; RNA BINDING PROTEIN;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; EMBRYO; EMBRYO DEVELOPMENT; GENE EXPRESSION; HUMAN; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY; VERTEBRATE; XENOPUS;

VERTEBRATA; XENOPUS;

EID: 2342512885     PISSN: 1526954X     EISSN: None     Source Type: Journal    
DOI: 10.1002/gene.20015     Document Type: Article

References (52)

1. Ahringer J, Rosenquist TA, Lawson DN, Kimble J. 1992. The Caenorhabditis elegans sex determining gene fem-3 is regulated posttranscriptionally. EMBO J 11:2303-2310.
2. Ballantyne S, Bilger A, Astrom J, Virtanen A, Wickens M. 1995. Poly(A) polymerases in the nucleus and cytoplasm of frog oocytes: dynamic changes during oocyte maturation and early development. RNA 1:64-78.
3. Castagnetti S, Ephrussi A. 2003. Orb and a long poly(A) tail are required for efficient oskar translation at the posterior pole of the Drosophila oocyte. Development 130:835-843.
4. Charlesworth A, Welk J, MacNicol AM. 2000. The temporal control of Wee1 mRNA translation during Xenopus oocyte maturation is regulated by cytoplasmic polyadenylation elements within the 3′-untranslated region. Dev Biol 227:706-719.
5. Chesnel F, Eppig JJ. 1995. Synthesis and accumulation of P34cdc2 and cyclin B in mouse oocytes during acquisition of competence to resume meiosis. Mol Reprod Dev 40:503-508.
6. Colgan DF, Manley JL. 1997. Mechanism and regulation of mRNA polyadenylation. Genes Dev 11:2755-2766.
7. de Moor CH, Richter JD. 1999. Cytoplasmic polyadenylation elements mediate masking and unmasking of cyclin B1 mRNA. EMBO J 18:2294-2303.
8. Dickson KS, Bilger A, Ballantyne S, Wickens MP. 1999. The cleavage and polyadenylation specificity factor in Xenopus laevis oocytes is a cytoplasmic factor involved in regulated polyadenylation. Mol Cell Biol 19:5707-5717.
9. Dworkin MB, Shrutkowsiki A, Dworkin-Rastl E. 1985. Mobilization of specific maternal RNA species into polysomes after fertilization in Xenopus laevis. Proc Natl Acad Sci USA 82:7636-7640.
10. Fox CA, Wickens M. 1990. Poly(A) removal during oocyte maturation: a default reaction selectively prevented by specific sequences in the 3′ UTR of certain maternal mRNAs. Genes Dev 4:2287-2298.
11. Fox CA, Sheets MD, Wickens MP. 1989. Poly(A) addition during maturation of frog oocytes: distinct nuclear and cytoplasmic activities and regulation by the sequence UUUUUAU. Genes Dev 3:2151-2162.
12. Fuchimoto D, Mizukoshi A, Schultz RM, Sakai S, Aoki F. 2001. Posttranscriptional regulation of cyclin A1 and cyclin A2 during mouse oocyte meiotic maturation and preimplantation development. Biol Reprod 65:986-993.
13. Gebauer F, Richter JD. 1995. Cloning and characterization of a Xenopus poly(A) polymerase. Mol Cell Biol 15:1422-1430.
14. Gebauer F, Xu W, Cooper GM, Richter JD. 1994. Translational control by cytoplasmic polyadenylation of c-mos mRNA is necessary for oocyte maturation in the mouse. EMBO J 13:5712.
15. Good PJ, Rebbert ML, Dawid IB. 1993. Three new members of the RNP protein family in Xenopus. Nucleic Acids Res 21:999-1006.
16. Good PJ, Chen QD, Warner SJ, Herring DC. 2000. A family of human RNA-binding proteins related to the Drosophila Bruno translational regulator. J Biol Chem 275:28583-28592.
17. Gray NK, Wickens M. 1998. Control of translation Initiation in animals. Annu Rev Cell Dev Biol 14:399-458.
18. Hake LE, Richter JD. 1994. CPEB is a specificity factor that mediates cytoplasmic polyadenylation during Xenopus oocyte maturation. Cell 79:617-627.
19. Huarte J, Stutz A, O'Connell ML, Gubler P, Belin D, Darrow AL, Strickland S, Vassalli JD. 1992. Transient translational silencing by reversible mRNA deadenylation. Cell 69:1021-1030.
20. Jin SW, Kimble J, Ellis RE. 2001. Regulation of cell fate in Caenorhabditis elegans by a novel cytoplasmic polyadenylation element binding protein. Dev Biol 229:537-553.
21. Hyman LE, Wormington WM. 1988. Translational inactivation of ribosomal protein mRNAs during Xenopus oocyte maturation. Genes Dev 2:598-605.
22. Kraemer B, Crittenden S, Gallegos M, Moulder G, Barstead R, Kimble J, Wickens M. 1999. NANOS-3 and FBF proteins physically interact to control the sperm-oocyte switch in Caenorhabditis elegans. Curr Biol 9:1009-1018.
23. Kubiak JZ, Weber M, de Pennart H, Winston NJ, Maro B. 1993. The metaphase II arrest in mouse oocytes is controlled through microtubule-dependent destruction of cyclin B in the presence of CSF. EMBO J 12:3773-3778.
24. Lieberfarb ME, Chu T, Wreden C, Theurkauf W, Gergen JP, Strickland S. 1996. Mutations that perturb poly(A)-dependent maternal mRNA activation block the initiation of development. Development 122:579-588.
25. Lisbin MJ, Gordon M, Yannoni YM, White K. 2000. Function of RRM domains of Drosophila melanogaster ELAV: RNP1 mutations and RRM domain replacements with ELAV family proteins and SXL. Genetics 155:1789-1798.
26. McGrew LL, Dworkin-Rastl E, Dworkin MB, Richter JD. 1989. Poly(A) elongation during Xenopus oocyte maturation is required for translational recruitment and is mediated by a short sequence element. Genes Dev 3:803-815.
27. Mendez R, Richter JD. 2001. Translational control by CPEB: a means to the end [Review]. Nat Rev Mol Cell Biol 2:521-529.
28. Mendez R, Hake LE, Andresson T, Littlepage LE, Ruderman JV, Richter JD. 2000a. Phosphorylation of CPE binding factor by Eg2 regulates translation of c-mos mRNA. Nature 404:302-307.
29. Mendez R, Murthy KGK, Ryan K, Manley JL, Richter JD. 2000b. Phosphorylation of CPEB by Eg2 mediates the recruitment of CPSF into an active cytoplasmic polyadenylation complex. Mol Cell 6:1253-1259.
30. Minshull J, Pines J, Golsteyn R, Standart N, Mackie S, Colman A, Blow J, Ruderman JV, Wu M, Hunt T. 1989. The role of cyclin synthesis, modification and destruction in the control of cell division. J Cell Sci Suppl 12:77-97.
31. Mitra J, Schultz RM. 1996. Regulation of the acquisition of meiotic competence in the mouse: changes in the subcellular localization of cdc2, cyclin B1, cdc25C and wee1, and in the concentration of these proteins and their transcripts. J Cell Sci 109:2407-2415.
32. Mueller PR, Coleman TR, Dunphy WG. 1995. Cell cycle regulation of a Xenopus Wee1-like kinase. Mol Biol Cell 6:119-134.
33. Nemeth A, Krause S, Blank D, Jenny A, Jeno P, Lustig A, Wahle E. 1995. Isolation of genomic and cDNA clones encoding bovine poly(A) binding protein II. Nucleic Acids Res 23:4034-4041.
34. Nieuwkoop PD, Faber J. 1956. Normal table of xenopus laevis (Daudin). North Holland Publishing, Amsterdam.
35. Paules RS, Buccione R, Moschel RC, Vande Woude GF, Eppig JJ. 1989. Mouse Mos protooncogene product is present and functions during oogenesis. Proc Natl Acad Sci USA 86:5395-5399.
36. Sachs AB, Bond MW, Kornberg RD. 1986. A single gene from yeast for both nuclear and cytoplasmic polyadenylate-binding proteins: domain structure and expression. Cell 45:827-835.
37. Sachs AB, Davis RW, Kornberg RD. 1987. A single domain of yeast poly(A)-binding protein is necessary and sufficient for RNA binding and cell viability. Mol Cell Biol 7:3268-3276.
38. Sagata N, Oskarsson M, Copeland T, Brumbaugh J, Vande Woude GF. 1988. Function of c-mos proto-oncogene product in meiotic maturation in Xenopus oocytes. Nature 335:519-525.
39. Salles FJ, Lieberfarb ME, Wreden C, Gergen JP, Strickland S. 1994. Coordinate initiation of Drosophila development by regulated polyadenylation of maternal messenger RNAs. Science 266:1996-1999.
40. Sambrook J, Fritsch EF, Maniatis T. 1989. Molecular Cloning: a laboratory manual. Cold Spring Harbor Laboratory Press.
41. Schisa JA, Strickland S. 1998. Cytoplasmic polyadenylation of Toll mRNA is required for dorsal-ventral patterning in Drosophila embryogenesis. Development 125:2995-3003.
42. Sheets MD, Wickens M. 1989. Two phases in the addition of a poly(A) tail. Genes Dev 3:1401-1412.
43. Sheets MD, Fox CA, Hunt T, Vande Woude G, Wickens M. 1994. The 3′-untranslated regions of c-mos and cyclin mRNAs stimulate translation by regulating cytoplasmic polyadenylation. Genes Dev 8:926-938.
44. Sheets MD, Wu M, Wickens M. 1995. Polyadenylation of c-mos mRNA as a control point in Xenopus meiotic maturation. Nature 374:511-516.
45. Stebbins-Boaz B, Hake LE, Richter JD. 1996. CPEB controls the cytoplasmic polyadenylation of cyclin, Cdk2 and c-mos mRNAs and is necessary for oocyte maturation in Xenopus. EMBO J 15:2582-2592.
46. Takagaki Y, Ryner LC, Manley JL. 1988. Separation and characterization of a poly(A) polymerase and a cleavage/specificity factor required for pre-mRNA polyadenylation. Cell 52:731-742.
47. Takagaki Y, Ryner LC, Manley JL. 1989. Four factors are required for 3′-end cleavage of pre-mRNAs. Genes Dev 3:1711-1724.
48. Voeltz GK, Ongkasuwan J, Standart N, Steitz JA. 2001. A novel embryonic poly(A) binding protein, ePAB, regulates mRNA deadenylation in Xenopus egg extracts. Genes Dev 15:774-788.
49. Wahle E. 1991. Purification and characterization of a mammalian polyadenylate polymerase involved in the 3′ end processing of messenger RNA precursors. J Biol Chem 266:3131-3139.
50. Wahle E. 1995. Poly(A) tail length control is caused by termination of processive synthesis. J Biol Chem 270:2800-2808.
51. Wahle E, Lustig A, Jeno P, Maurer P. 1993. Mammalian poly(A)-binding protein II. Physical properties and binding to polynucleotides. J Biol Chem 268:2937-2945.
52. Zhang B, Gallegos M, Puoti A, Durkin E, Fields S, Kimble J, Wickens MP. 1997. A conserved RNA-binding protein that regulates sexual fates in the C. elegans hermaphrodite germ line. Nature 390:477-484.