The Internal Ribosome Entry Site-Mediated Translation of Antiapoptotic Protein XIAP Is Modulated by the Heterogeneous Nuclear Ribonucleoproteins C1 and C2

REFERENCES

• Brockstedt, E., A. Rickers, S. Kostka, A. Laubersheimer, B. Dorken, B. Wittmann-Liebold, K. Bommert, and A. Otto. 1998. Identification of apoptosis-associated proteins in a human Burkitt lymphoma cell line. Cleavage ofheterogeneous nuclear ribonucleoprotein A1 by caspase 3. J. Biol. Chem. 273: 28057–28064.
   PubMed Web of Science ®Google Scholar
• Burd, C. G., M. S. Swanson, M. Gorlach, and G. Dreyfuss. 1989. Primary structures of the heterogeneous nuclear ribonucleoprotein A2, B1, and C2 proteins: a diversity of RNA binding proteins is generated by small peptide inserts. Proc. Natl. Acad. Sci. USA 86: 9788–9792.
   PubMed Web of Science ®Google Scholar
• Chan, E. K., and E. M. Tan. 1987. Human autoantibody-reactive epitopes of SS-B/La are highly conserved in comparison with epitopes recognized by murine monoclonal antibodies. J. Exp. Med. 166: 1627–1640.
   PubMed Web of Science ®Google Scholar
• Choi, Y. D., P. J. Grabowski, P. A. Sharp, and G. Dreyfuss. 1986. Heterogeneous nuclear ribonucleoproteins: role in RNA splicing. Science 231: 1534–1539.
   PubMed Web of Science ®Google Scholar
• Coldwell, M. J., S. A. Mitchell, M. Stoneley, M. MacFarlane, and A. E. Willis. 2000. Initiation of Apaf-1 translation by internal ribosome entry. Oncogene 19: 899–905.
   PubMed Web of Science ®Google Scholar
• Ford, L. P., J. M. Suh, W. E. Wright, and J. W. Shay. 2000. Heterogeneous nuclear ribonucleoproteins C1 and C2 associate with the RNA component of human telomerase. Mol. Cell. Biol. 20: 9084–9091.
   PubMed Web of Science ®Google Scholar
• Gorlach, M., C. G. Burd, and G. Dreyfuss. 1994. The determinants of RNA-binding specificity of the heterogeneous nuclear ribonucleoprotein C proteins. J. Biol. Chem. 269: 23074–23078.
   PubMedGoogle Scholar
• Hamilton, B. J., E. Nagy, J. S. Malter, B. A. Arrick, and W. F. Rigby. 1993. Association of heterogeneous nuclear ribonucleoprotein A1 and C proteins with reiterated AUUUA sequences. J. Biol. Chem. 268: 8881–8887.
   PubMed Web of Science ®Google Scholar
• Hellen, C. U., and P. Sarnow. 2001. Internal ribosome entry sites in eukaryotic mRNA molecules. Genes Dev. 15: 1593–1612.
   PubMed Web of Science ®Google Scholar
• Holcik, M., H. Gibson, and R. G. Korneluk. 2001. XIAP: apoptotic brake and promising therapeutic target. Apoptosis 6: 253–261.
   PubMed Web of Science ®Google Scholar
• Holcik, M., and R. G. Korneluk. 2000. Functional characterization of the X-linked inhibitor of apoptosis (XIAP) internal ribosome entry site element: role of La autoantigen in XIAP translation. Mol. Cell. Biol. 20: 4648–4657.
   PubMed Web of Science ®Google Scholar
• Holcik, M., and R. G. Korneluk. 2001. XIAP, the guardian angel. Nat. Rev. Mol. Cell Biol. 2: 550–556.
   PubMed Web of Science ®Google Scholar
• Holcik, M., C. A. Lefebvre, C. Yeh, T. Chow, and R. G. Korneluk. 1999. A new internal-ribosome-entry-site motif potentiates XIAP-mediated cytoprotection. Nat. Cell Biol. 1: 190–192.
   PubMed Web of Science ®Google Scholar
• Holcik, M., and S. A. Liebhaber. 1997. Analysis of mRNP complexes assembled in vitro, p. 195–209. In J. Richter (ed.), mRNA formation and function. Academic Press, New York, N.Y.
   Google Scholar
• Holcik, M., N. Sonenberg, and R. G. Korneluk. 2000. Internal ribosome initiation of translation and the control of cell death. Trends Genet. 16: 469–473.
   PubMedGoogle Scholar
• Holcik, M., C. Yeh, R. G. Korneluk, and T. Chow. 2000. Translational upregulation of X-linked inhibitor of apoptosis (XIAP) increases resistance to radiation-induced cell death. Oncogene 19: 4174–4177.
   PubMed Web of Science ®Google Scholar
• Huez, I., L. Creancier, S. Audigier, M. C. Gensac, A. C. Prats, and H. Prats. 1998. Two independent internal ribosome entry sites are involved in translation initiation of vascular endothelial growth factor mRNA. Mol. Cell. Biol. 18: 6178–6190.
   PubMed Web of Science ®Google Scholar
• Iizuka, N., C. Chen, Q. Yang, G. Johannes, and P. Sarnow. 1995. Cap-independent translation and internal initiation of translation in eukaryotic cellular mRNA molecules. Curr. Top. Microbiol. Immunol. 203: 155–177.
   PubMedGoogle Scholar
• Jackson, R. J. 2000. A comparative view of initiation site selection mechanisms, p. 127–183. In N. Sonenberg, J. W. B., Hershey,, and M. B. Mathews (ed.), Translational control of gene expression. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
   Google Scholar
• Kiledjian, M., C. G. Burd, M. Gorlach, D. S. Portman, and G. Dreyfuss. 1994. Structure and function of hnRNP proteins, p. 127–149. In I. Mattaj and K. Nagai (ed.), RNA protein interactions. Oxford University Press, Oxford, United Kingdom.
   Google Scholar
• LaCasse, E. C., S. Baird, R. G. Korneluk, and A. E. MacKenzie. 1998. The inhibitors of apoptosis (IAPs) and their emerging role in cancer. Oncogene 17: 3247–3259.
   PubMed Web of Science ®Google Scholar
• MacGregor, G. R., G. P. Nolan, S. Fiering, M. Roederer, and L. A. Herzenberg. 1991. Use of E. coli lacZ (β-galactosidase) as a reporter gene, p. 217–235. In E. J. Murray and J. M. Walker (ed.), Methods in molecular biology, vol. 7. Humana Press Inc., Clifton, N.J.
   Google Scholar
• Martinez-Salas, E., R. Ramos, E. Lafuente, and S. Lopez De Quinto. 2001. Functional interactions in internal translation initiation directed by viral and cellular IRES elements. J. Gen. Virol. 82: 973–984.
   PubMedGoogle Scholar
• Mathews, D. H., J. Sabina, M. Zuker, and D. H. Turner. 1999. Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. J. Mol. Biol. 288: 911–940.
   PubMed Web of Science ®Google Scholar
• Millard, S. S., A. Vidal, M. Markus, and A. Koff. 2000. A U-rich element in the 5′ untranslated region is necessary for the translation of p27 mRNA. Mol. Cell. Biol. 20: 5947–5959.
   PubMed Web of Science ®Google Scholar
• Miskimins, W. K., G. Wang, M. Hawkinson, and R. Miskimins. 2001. Control of cyclin-dependent kinase inhibitor p27 expression by cap-independent translation. Mol. Cell. Biol. 21: 4960–4967.
   PubMedGoogle Scholar
• Nanbu, R., L. Montero, D. D'Orazio, and Y. Nagamine. 1997. Enhanced stability of urokinase-type plasminogen activator mRNA in metastatic breast cancer MDA-MB-231 cells and LLC-PK1 cells down-regulated for protein kinase C—correlation with cytoplasmic heterogeneous nuclear ribonucleoprotein C. Eur. J. Biochem. 247: 169–174.
   PubMedGoogle Scholar
• Rajagopalan, L. E., C. J. Westmark, J. A. Jarzembowski, and J. S. Malter. 1998. hnRNP C increases amyloid precursor protein (APP) production by stabilizing APP mRNA. Nucleic Acids Res. 26: 3418–3423.
   PubMedGoogle Scholar
• Reed, J. C. 1999. Dysregulation of apoptosis in cancer. J. Clin. Oncol 17: 2941–2953.
   PubMed Web of Science ®Google Scholar
• Sella, O., G. Gerlitz, S.-Y. Le, and O. Elroy-Stein. 1999. Differentiation-induced internal translation of c-sis mRNA: analysis of the cis elements and their differentiation-linked binding to the hnRNP C protein. Mol. Cell. Biol. 19: 5429–5440.
   PubMedGoogle Scholar
• Seto, A. G., A. J. Zaug, S. G. Sobel, S. L. Wolin, and T. R. Cech. 1999. Saccharomyces cerevisiae telomerase is an Sm small nuclear ribonucleoprotein particle. Nature 401: 177–180.
   PubMed Web of Science ®Google Scholar
• Soltaninassab, S. R., J. G. McAfee, L. Shahied-Milam, and W. M. LeStourgeon. 1998. Oligonucleotide binding specificities of the hnRNP C protein tetramer. Nucleic Acids Res. 26: 3410–3417.
   PubMed Web of Science ®Google Scholar
• Stoneley, M., T. Subkhankulova, J. P. Le Quesne, M. J. Coldwell, C. L. Jopling, G. J. Belsham, and A. E. Willis. 2000. Analysis of the c-myc IRES; a potential role for cell-type specific trans-acting factors and the nuclear compartment. Nucleic Acids Res. 28: 687–694.
   PubMedGoogle Scholar
• Thiede, B., C. Dimmler, F. Siejak, and T. Rudel. 2001. Predominant identification of RNA-binding proteins in Fas-induced apoptosis by proteome analysis. J. Biol. Chem. 276: 26044–26050.
   PubMed Web of Science ®Google Scholar
• Wang, X. Y., P. E. Hoyle, and J. A. McCubrey. 1998. Characterization of proteins binding the 3′ regulatory region of the IL-3 gene in IL-3-dependent and autocrine-transformed hematopoietic cells. Leukemia 12: 520–531.
   PubMedGoogle Scholar
• Waterhouse, N., S. Kumar, Q. Song, P. Strike, L. Sparrow, G. Dreyfuss, E. S. Alnemri, G. Litwack, M. Lavin, and D. Watters. 1996. Heteronuclear ribonucleoproteins C1 and C2, components of the spliceosome, are specific targets of interleukin 1beta-converting enzyme-like proteases in apoptosis. J. Biol. Chem. 271: 29335–29341.
   PubMedGoogle Scholar
• Williamson, D. J., S. Banik-Maiti, J. DeGregori, and H. E. Ruley. 2000. hnRNP C is required for postimplantation mouse development but is dispensable for cell viability. Mol. Cell. Biol. 20: 4094–4105.
   PubMedGoogle Scholar
• Wilusz, J., and T. Shenk. 1990. A uridylate tract mediates efficient heterogeneous nuclear ribonucleoprotein C protein-RNA cross-linking and functionally substitutes for the downstream element of the polyadenylation signal. Mol. Cell. Biol. 10: 6397–6407.
   PubMed Web of Science ®Google Scholar
• Zaidi, S. H., and J. S. Malter. 1995. Nucleolin and heterogeneous nuclear ribonucleoprotein C proteins specifically interact with the 3′-untranslated region of amyloid protein precursor mRNA. J. Biol. Chem. 270: 17292–17298.
   PubMedGoogle Scholar
• Zuker, M., D. H. Mathews, and D. H. Turner. 1999. Algorithms and thermodynamics for RNA secondary structure prediction: a practical guide, p. 11–43. In B. F. Clark and J. Barciszewski (ed.), RNA biochemistry and biotechnology. Proceedings of the NATO Advanced Research Workshop on RNA Biochemistry and Biotechnology. Kluwer Academic Publishers, Dordrecht, The Netherlands.
   Google Scholar