Erythroid Cell-Specific mRNA Stability Elements in the α2-Globin 39 Nontranslated Region

REFERENCES

• Atwater, J. A., R. Wisdom, and I. M. Verma. 1990. Regulated mRNA stability. Annu. Rev. Genet. 24:519–641.
   PubMed Web of Science ®Google Scholar
• Aviv, H., Z. Volloch, R. Bastos, and S. Levy. 1976. Biosynthesis and stability of globin mRNA in erythroleukemia friend cells. Cell 8:495–503.
   PubMed Web of Science ®Google Scholar
• Bandyopadhyay, R., M. Coutts, A. Krowczynska, and G. Brawerman. 1990. Nuclease activity associated with mammalian mRNA in its native state: possible basis for selectivity in mRNA decay. Mol. Cell. Biol. 10:2060–2069.
   PubMed Web of Science ®Google Scholar
• Banerjee, A. K. 1980. 59-terminal cap structure in eucaryotic messenger ribonucleic acids. Microbiol. Rev. 44:175–205.
   PubMedGoogle Scholar
• Barker, G. F., and K. Beemon. 1994. Rous sarcoma virus RNA stability requires an open reading frame in the gag gene and sequences downstream of the gag-pol junction. Mol. Cell. Biol. 14:1986–1996.
   PubMedGoogle Scholar
• Bastos, R. N., and H. Aviv. 1977. Theoretical analysis of a model for globin messenger RNA accumulation during erythropoiesis. J. Mol. Biol. 110:204–218.
   Google Scholar
• Bastos, R. N., Z. Volloch, and H. Aviv. 1977. Messenger RNA population analysis during erythroid differentiation: a kinetic approach. J. Mol. Biol. 110:191–203.
   PubMed Web of Science ®Google Scholar
• Belasco, J., and G. Brawerman. 1993. Control of mRNA stability. Academic Press, San Diego, Calif.
   Google Scholar
• Bernstein, P., S. W. Peltz, and J. Ross. 1989. The poly(A)-binding protein complex is a major determinant of mRNA stability in vitro. Mol. Cell. Biol. 9:659–670.
   PubMed Web of Science ®Google Scholar
• Bunn, H. F., G. J. Schmidt, D. N. Haney, and R. G. Dluhy. 1975. Hemoglobin Cranston, an unstable variant having an elongated β chain due to nonho-mologous crossover between two normal β chain genes. Proc. Natl. Acad. Sci. USA 72:3609–3613.
   PubMed Web of Science ®Google Scholar
• Caponigro, G., D. Muhlrad, and R. Parker. 1993. A small segment of the MATα1 transcript promotes mRNA decay in Saccharomyces cerevisiae: a stimulatory role for rare codons. Mol. Cell. Biol. 13:5141–5148.
   PubMed Web of Science ®Google Scholar
• Casey, J. L., M. W. Hentze, D. M. Koeller, S. W. Caughman, T. A. Rouault, R. D. Klausner, and J. B. Harford. 1988. Iron-responsive elements: regulatory RNA sequences that control mRNA levels and translation. Science 240:924–928.
   PubMed Web of Science ®Google Scholar
• Clegg, J. B., D. J. Weatherall, and P. F. Milner. 1971. Haemoglobin Constant Spring—a chain termination mutant? Nature (London) 234: 337–340.
   PubMed Web of Science ®Google Scholar
• Decker, C. J., and R. Parker. 1993. A turnover pathway for both stable and unstable mRNAs in yeast: evidence for a requirement for deadenylation. Genes Dev. 7:1632–1643.
   PubMed Web of Science ®Google Scholar
• Dodson, R. E., and D. J. Shapiro. 1994. An estrogen-inducible protein binds specifically to a sequence in the 39 untranslated region of estrogen-stabilized vitellogenin mRNA. Mol. Cell. Biol. 14:3130–3138.
   PubMed Web of Science ®Google Scholar
• Flatz, G., J. L. Kinderlerer, J. V. Kilmartin, and H. Lehman. 1971. Haemoglobin Tak: a variant with additional residues at the end of the β-chains. Lancet i:732–733.
   Google Scholar
• Furuichi, Y., A. La Fiandra, and A. J. Shatkin. 1977. 59-terminal structure and mRNA stability. Nature (London) 266:235–239.
   PubMedGoogle Scholar
• Greenberg, M. E., and E. B. Ziff. 1984. Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogene. Nature (London) 311:433–438.
   PubMed Web of Science ®Google Scholar
• Hargrove, J. L., and F. H. Schmidt. 1989. The role of mRNA and protein stability in gene expression. FASEB J. 3:2360–2370.
   PubMed Web of Science ®Google Scholar
• Herrick, D. J., and J. Ross. 1994. The half-life of c-myc mRNA in growing and serum-stimulated cells: influence of the coding and 39 untranslated regions and the role of ribosome translocation. Mol. Cell. Biol. 14:2119–2128.
   PubMed Web of Science ®Google Scholar
• Ho, S. N., H. D. Hunt, R. M. Horton, J. K. Pullen, and L. R. Pease. 1989. Site-directed mutagenesis by overlap extension using the polymerase chain reaction. Gene 77:51–59.
   PubMed Web of Science ®Google Scholar
• Horton, R. M., H. D. Hunt, S. N. Ho, J. K. Pullen, and L. R. Pease. 1989. Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension. Gene 77:61–68.
   PubMed Web of Science ®Google Scholar
• Hunt, D. M., D. R. Higgs, P. Winichagoon, J. B. Clegg, and D. J. Weatherall. 1982. Haemoglobin Constant Spring has an unstable α chain messenger RNA. Br. J. Haematol. 51:405–413.
   PubMed Web of Science ®Google Scholar
• Jackson, R. J., and N. Standart. 1990. Do the poly (A) tail and 39 untranslated region control mRNA translation? Cell 62:15–24.
   PubMed Web of Science ®Google Scholar
• Kabnick, K. S., and D. E. Housman. 1988. Determinants that contribute to cytoplasmic stability of human c-fos and β-globin mRNAs are located at several sites in each mRNA. Mol. Cell. Biol. 8:3244–3250.
   PubMed Web of Science ®Google Scholar
• Kan, Y. W., D. Todd, and A. M. Dozy. 1974. Haemoglobin Constant Spring synthesis in red cell precursors. Br. J. Haematol. 28:103–107.
   PubMed Web of Science ®Google Scholar
• Klausner, R. D., T. A. Rouault, and J. B. Harford. 1993. Regulating the fate of mRNA: the control of cellular iron metabolism. Cell 72:19–28.
   PubMed Web of Science ®Google Scholar
• Kozak, M., and A. J. Shatkin. 1977. Sequences of two 59-terminal ribosome-protected fragments from reovirus messenger RNAs. J. Mol. Biol. 112:75–96.
   PubMedGoogle Scholar
• Krowczynska, A., R. Yenofsky, and G. Brawerman. 1985. Regulation of messenger RNA stability in mouse erythroleukemia cells. J. Mol. Biol. 181: 231–239.
   PubMedGoogle Scholar
• Langstaff, J. M., and H. R. V. Arnstein. 1985. Messenger RNA turnover during bone marrow erythroid cell differentiation. Biochim. Biophys. Acta 825:316–325.
   PubMedGoogle Scholar
• Liebhaber, S. A., E.-U. Griese, I. Weiss, F. E. Cash, H. Ayyub, D. R. Higgs, and J. Horst. 1990. Inactivation of human α-globin gene expression by a de novo deletion located upstream of the α-globin gene cluster. Proc. Natl. Acad. Sci. USA 87:9431–9435.
   PubMed Web of Science ®Google Scholar
• Liebhaber, S. A., and Y. W. Kan. 1981. Differentiation of the mRNA transcripts originating from the α1- and α2-globin loci in normals and α-thalas-semics. J. Clin. Invest. 68:439–446.
   PubMed Web of Science ®Google Scholar
• Lodish, H. F., and B. Small. 1976. Different lifetimes of reticulocyte messenger RNA. Cell 7:59–65.
   PubMed Web of Science ®Google Scholar
• Lumelsky, N. L., and B. G. Forget. 1991. Negative regulation of globin gene expression during megakaryocytic differentiation of a human erytholeukemic cell line. Mol. Cell. Biol. 11:3528–3536.
   PubMedGoogle Scholar
• Meyuhas, O., and R. P. Perry. 1980. Construction and identification of cDNA clones for mouse ribosomal proteins: application for the study of r-protein gene expression. Gene 10:113–129.
   PubMed Web of Science ®Google Scholar
• Milner, P. F., J. B. Clegg, and D. J. Weatherall. 1971. Haemoglobin-H disease due to a unique haemoglobin variant with an elongated α-chain. Lancet 10:729–732.
   Google Scholar
• Muhlrad, D., C. J. Decker, and R. Parker. 1994. Deadenylation of the unstable mRNA encoded by the yeast MFA2 gene leads to decapping followed by 59 3 39 digestion of the transcript. Genes Dev. 8:855–866.
   PubMed Web of Science ®Google Scholar
• Nielson, D. A., and D. J. Shapiro. 1990. Insights into hormonal control of messenger RNA stability. Mol. Endocrinol. 4:953–957.
   PubMedGoogle Scholar
• Nienhuis, A. W., and E. J. Benz, Jr. 1977. Regulation of hemoglobin synthesis during the development of the red cell. N. Engl. J. Med. 297:1318–1328.
   PubMed Web of Science ®Google Scholar
• Osley, M. A. 1991. The regulation of histone synthesis in the cell cycle. Annu. Rev. Biochem. 60:827–861.
   PubMed Web of Science ®Google Scholar
• Peltz, S. W., G. Brewer, P. Bernstein, P. A. Hartford, and J. Ross. 1991. Regulation of mRNA turnover in eucaryotic cells. Crit. Rev. Eukaryotic Gene Expr. 1:99–126.
   PubMedGoogle Scholar
• Peltz, S. W., and A. Jacobson. 1992. mRNA stability: in trans-it. Curr. Opin. Cell Biol. 4:979–983.
   PubMedGoogle Scholar
• Petersen, D. D., S. R. Koch, and D. K. Granner. 1989. 39 noncoding region of phosphoenolpyruvate carboxykinase mRNA contains a glucocorticoid-responsive mRNA-stabilizing element. Proc. Natl. Acad. Sci. USA 86:7800–7804.
   PubMedGoogle Scholar
• Ross, J., and A. Pizarro. 1983. Human beta and delta messenger RNAs turnover at different rates. J. Mol. Biol. 167:607–617.
   PubMedGoogle Scholar
• Ross, J., and T. D. Sullivan. 1985. Half-lives of beta and gamma globin messenger RNAs and of protein synthetic capacity in cultured human re-ticulocytes. Blood 66:1149–1154.
   PubMed Web of Science ®Google Scholar
• Sanger, F., S. Nicklen, and A. R. Coulson. 1977. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74:5463–5467.
   PubMed Web of Science ®Google Scholar
• Shapiro, D. J., J. E. Blume, and D. A. Nielson. 1987. Regulation of messenger RNA stability in eucaryotic cells. Bioessays 5:221–226.
   Google Scholar
• Treisman, R. 1985. Transient accumulation of c-fos RNA following serum starvation requires a conserved 59 element and c-fos 39 sequences. Cell 42:889–902.
   PubMed Web of Science ®Google Scholar
• Volloch, V., and D. Housman. 1981. Stability of globin mRNA in terminally differentiating murine erythroleukemia cells. Cell 23:509–514.
   PubMed Web of Science ®Google Scholar
• Vreken, P., and H. A. Raue. 1992. The rate-limiting step in yeast PGK1 mRNA degradation is an endonucleolytic cleavage in the 39-terminal part of the coding region. Mol. Cell. Biol. 12:2986–2996.
   PubMedGoogle Scholar
• Wang, X., M. Kiledjian, I. Weiss, and S. A. Liebhaber. 1995. Detection and characterization of a 39 untranslated region ribonucleoprotein complex associated with human α-globin mRNA stability. Mol. Cell. Biol. 15:1769–1777.
   PubMedGoogle Scholar
• Weiss, I., F. E. Cash, M. B. Coleman, A. Pressley, J. G. Adams, T. San-guansermsri, S. A. Liebhaber, and M. H. Steinberg. 1990. Molecular basis for α thalassemia associated with the structural mutant hemoglobin Suan-Dok (α2109LEU3ARG). Blood 76:2630–2636.
   PubMed Web of Science ®Google Scholar
• Weiss, I. M., and S. A. Liebhaber. 1994. Erythroid cell-specific determinants of α-globin mRNA stability. Mol. Cell. Biol. 14:8123–8132.
   PubMed Web of Science ®Google Scholar
• Wellington, C. L., M. E. Greenberg, and J. G. Belasco. 1993. The destabi-lizing elements in the coding region of c-fos mRNA are recognized as RNA. Mol. Cell. Biol. 13:5034–5042.
   PubMedGoogle Scholar
• Wolin, S. L., and P. Walter. 1988. Ribosome pausing and stacking during translation of a eukaryotic mRNA. EMBO J. 7:3559–3569.
   PubMed Web of Science ®Google Scholar
• Wreschner, D. H., and G. Rechavi. 1987. Differential mRNA stability to reticulocyte ribonucleases correlates with 39 non-coding (U)nA sequences. Eur. J. Biochem. 87:333–340.
   Google Scholar
• Yamada, M., S. Hudson, O. Tournay, S. Bittenbender, S. S. Shane, B. Lange, Y. Tsujimoto, A. J. Caton, and G. Rovera. 1989. Detection of minimal disease in hematopoietic malignancies of the B-cell lineage by using third-complementarity-determining region (CDR-III)-specific probes. Proc. Natl. Acad. Sci. USA 86:5123–5127.
   PubMed Web of Science ®Google Scholar
• Yen, T. J., P. S. Machlin, and D. W. Cleveland. 1988. Autoregulated instability of β-tubulin mRNAs by recognition of the nascent amino terminus of β-tubulin. Nature (London) 334:580–585.
   PubMed Web of Science ®Google Scholar
• Zoller, M. J., and M. Smith. 1982. Oligonucleotide-directed mutagenesis using M13-derived vectors: an efficient and general procedure for the production of point mutations in any fragment of DNA. Nucleic Acids Res. 10:6487–6500.
   PubMed Web of Science ®Google Scholar
• Zuker, M., and P. Stiegler. 1981. Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information. Nucleic Acids Res. 9:133–148.
   PubMed Web of Science ®Google Scholar