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  • Basak, A., Ozer, A., Kirdar, B. & Akar, N. (1993) A novel 13 bp deletion in the 3′UTR of the β-globin gene causes β-thalassemia in a Turkish patient. Hemoglobin, 17, 551555.
  • Bunn, H.F., Schmidt, G.J., Haney, D.N. & Dluhy, R.G. (1975) Hemoglobin Cranston, an unstable variant having an elongated beta chain due to non-homologous crossover between two normal beta chain genes. Proceedings of the National Academy of Sciences of the USA, 72, 36093613.
  • Cai, S.P., Eng, B., Francombe, W.H., Olivieri, N.F., Kendall, A.G., Waye, J.S. & Chui, D.H. (1992) Two novel beta-thalassemia mutations in the 5′ and 3′ non-coding regions of the beta-globin gene. Blood, 79, 13421346.
  • Casey, J.L., Koeller, D.M., Ramin, V.C., Klausner, R.D. & Harford, J.B. (1989) Iron regulation of transferrin receptor mRNA levels requires iron-responsive elements and a rapid turnover determinant in the 3′ untranslated region of the mRNA. EMBO Journal, 8, 36933699.
  • Colgan, D.F. & Manley, J.L. (1997) Mechanism and regulation of mRNA polyadenylation. Genes and Development, 11, 27552766.
  • Curtin, P., Pirastu, M., Kan, Y.W., Gobert-Jones, J.A., Stephens, A.D. & Lehmann, H. (1985) A distant gene deletion affects β-globin gene function in atypical γδβ-thalassemia. Journal of Clinical Investigation, 76, 15541558.
  • Czyzyk-Krzeska, M.F. & Beresh, J.E. (1996) Characterization of the hypoxia-inducible protein binding site within the pyrimidine-rich tract in the 3′-untranslated region of the tyrosine hydroxylase mRNA. Journal of Biological Chemistry, 271, 32933299.
  • De Jong, W.W., Meera Khan, P. & Bernini, L.F. (1975) Hemoglobin Koya Dora: high frequency of a chain termination mutant. American Journal of Human Genetics, 27, 8190.
  • Del Gatto-Konczak, F., Olive, M., Gesnel, M. & Breathnach, R. (1999) hnRNP A1 recruited to an exon in vivo can function as an exon splicing silencer. Molecular and Cellular Biology, 19, 251260.
  • Delanoe-Garin, J., Blouquit, Y., Arous, N., Kister, J., Poyart, C., North, M.L., Bardakdjian, J., Lacombe, C., Rosa, J. & Galacteros, F. (1988) Hemoglobin Saverne: a new variant with elongated beta chains: structural and functional properties. Hemoglobin, 12, 337352.
  • Driscoll, M.C., Dobkin, C.S. & Alter, B.P. (1989) γδβ-thalassemia due to a de novo mutation deleting the 5′β-globin gene activation-region hypersensitive sites. Proceedings of the National Academy of Sciences of the USA, 86, 74707474.
  • Eckner, R., Elmeier, W. & Birnstiel, M.L. (1991) Mature mRNA 3′ end formation stimulates RNA export from the nucleus. EMBO Journal, 10, 35133522.
  • Flatz, G., Kinderlerer, J.L., Kilmartin, J.V. & Lehmann, H. (1971) Haemoglobin Tak: a variant with additional residues at the end of the beta-chains. Lancet, 1, 732733.
  • Hamm, J. & Mattaj, I.W. (1990) Monomethylated cap structures facilitate RNA export from the nucleus. Cell, 109118.
  • Hanash, S.M., Winter, W.P. & Rucknagel, D.L. (1977) Synthesis of haemoglobin Wayne in erythroid cells. Nature, 269, 717719.
  • Hastings, M.L. & Krainer, A.R. (2000) Pre-mRNA splicing in the new millennium. Current Opinions in Cell Biology, 13, 302309.
  • Hentze, M.W., Caughmanman, S.W., Rouault, T.A., Barriocanal, J.G., Dancis, A., Harford, J.B. & Klausner, R.D. (1987) Identification of the iron-responsive element for the translational regulation of human ferritin mRNA. Science, 238, 15701573.
  • Holcik, M. & Liebhaber, S.A. (1997) Four highly stable eukaryotic mRNAs assemble 3′UTR RNA-protein complexes sharing cis- and trans-components. Proceedings of the National Academy of Sciences of the USA, 94, 24102414.
  • Hunt, D.M., Higgs, D.R., Winichagoon, P., Clegg, J.B. & Weatherall, D.J. (1982) Hemoglobin Constant Spring has an unstable α-chain messenger RNA. British Journal of Haematology, 51, 405413.
  • Jankovic, L., Efremov, G.D., Petkov, G., Kattamis, C., George, E., Yang, K-G., Stoming, T.A. & Huisman, T.H.J. (1990) Two novel polyadenylation mutations leading to beta (+) thalassemia. British Journal of Haematology, 75, 122126.
  • Jankovic, L., Dimovsky, A.J., Kollia, P., Loukopoulous, D. & Huisman, T.H.J. (1991) A C–G mutation at nt position 6 3′ to the terminating codon may be the cause of a silent beta-thalassemia. International Journal of Hematology, 54, 289293.
  • Jarmolowski, A., Boelens, W.C., Izaurralde, E. & Mattaj, I.W. (1994) Nuclear transport of different classes of RNA is mediated by specific factors. EMBO Journal, 12, 223232.
  • Kabnick, K.S. & Housman, D.E. (1988) Determinants that contribute to cytoplasmic stability of human c-fos and β-globin mRNAs are located at several sites in each mRNA. Molecular and Cellular Biology, 8, 32443250.
  • Kiledjian, M., Wang, X. & Liebhaber, S.A. (1995) Identification of two KH domain proteins in the alpha-globin mRNP stability complex. EMBO Journal, 14, 43574364.
  • Klausner, R.D., Rouault, T.A. & Harford, J.B. (1993) Regulating the fate of mRNA: the control of cellular iron metabolism. Cell, 72, 1928.
  • Kozak, M. (1987) An analysis of 5′-non-coding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Research, 15, 81258148.
  • Kozak, M. (1994) Features in the 5′ non-coding sequences of rabbit α- and β-globin mRNAs that affect translational efficiency. Journal of Molecular Biology, 235, 95110.
  • Kozak, M. (1999) Initiation of translation in prokaryotes and eukaryotes. Gene, 234, 187208.
  • Liebhaber, S.A. & Kan, Y.W. (1981) Differentiation of the mRNA transcripts originating from the alpha (1)- and alpha (2)-globin loci in normals and alpha thalassemics. Journal of Clinical Investigation, 68.
  • Liebhaber, S.A., Wang, Z., Cash, F., Monks, B. & Russell, J.E. (1996) Developmental silencing of the embryonic zeta-globin gene: concerted action of the promoter and the 3′ flanking region combined with stage-specific silencing of the transcribed region. Molecular and Cellular Biology, 16, 26372646.
  • Lodish, H.F. & Small, B. (1976) Different lifetimes of reticulocyte messenger RNA. Cell, 7, 5965.
  • Mayeda, A., Screaton, G.R., Chandler, S.D., Fu, X.D. & Krainer, A.D. (1999) Substrate specificities of SR proteins in constitutive splicing are determined by their RNA recognition motifs and composite pre-mRNA exonic elements. Molecular and Cellular Biology, 19, 18531863.
  • Morales, J., Russell, J.E. & Liebhaber, S.A. (1997) Destabilization of human alpha-globin mRNA by translation anti-termination is controlled during erythroid terminal differentiation and paralleled by phased shortening of the poly(A) tail. Journal of Biological Chemistry, 272, 66076613.
  • Nakielny, S., Fischer, U., Michael, W.M. & Dreyfuss, G. (1997) RNA transport. Annual Review of Neuroscience, 20, 269301.
  • Orkin, S.H., Cheng, T-C., Antonarakis, S.E. & Kazazian, H.H. (1985) Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human β-globin gene. EMBO Journal, 4, 453456.
  • Ostareck-Lederer, A., Ostareck, D.H., Standart, N. & Thiele, B.J. (1994) Translation of 15-lipoxygenase mRNA is inhibited by a protein that binds to a repeated sequence in the 3′ untranslated region. EMBO Journal, 13, 14761481.
  • Pandey, N.B. & Marzluff, W.F. (1987) The stem-loop structure at the 3′ end of histone mRNA is necessary and sufficient for regulation of histone mRNA stability. Molecular and Cellular Biology, 7, 45574559.
  • Reed, R. (2000) Mechanisms of fidelity in pre-mRNA splicing. Current Opinions in Cell Biology, 12, 340345.
  • Ross, J. & Pizarro, A. (1983) Human beta and delta globin messenger RNAs turn over at different rates. Journal of Molecular Biology, 167, 607617.
  • Ross, J. & Sullivan, T.D. (1985) Half-lives of beta and gamma globin messenger RNAs and of protein synthetic capacity in cultured human reticulocytes. Blood, 66, 11491154.
  • Russell, J.E. & Liebhaber, S.A. (1993) Molecular genetics of thalassemia. In: Advances in Genome Biology (ed. by R.S.Verma), Vol. 2, pp. 283353. JAI Press, Greenwich.
  • Russell, J.E. & Liebhaber, S.A. (1996) The stability of human beta-globin mRNA is dependent on structural determinants positioned within its 3′ untranslated region. Blood, 87, 53145323.
  • Russell, J.E., Morales, J., Makeyev, A. & Liebhaber, S.A. (1998) Sequence divergence in the 3′UTRs of human zeta- and alpha-globin mRNA mediates a difference in their stabilities and contributes to efficient zeta-to-alpha gene developmental switching. Molecular and Cellular Biology, 18, 21732183.
  • Scheper, W., Meinsma, D., Holthuizen, P.E. & Sussenbach, J.S. (1995) Long–range RNA interaction of two sequence elements required for endonucleolytic cleavage of human insulin-like growth factor II mRNAs. Molecular and Cellular Biology, 15, 235245.
  • Shaw, G. & Kamen, R. (1986) A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradation. Cell, 46, 659667.
  • Shyu, A.B., Greenberg, M.E. & Belasco, J.G. (1989) The c-fos transcript is targeted for rapid decay by two distinct mRNA degradation pathways. Genes and Development, 3, 6072.
  • Stefanovic, B., Hellerbrand, C., Holcik, M., Briendl, M.A., Liebhaber, S. & Brenner, D.A. (1997) Post-transcriptional regulation of collagen alpha1 (I) mRNA in hepatic satellite cells. Molecular and Cellular Biology, 17, 52015209.
  • Talbot, D., Collis, P., Antoniou, M., Vidal, M., Grosveld, F. & Greaves, D.R. (1989) A dominant control region from human beta-globin locus conferring integration site-independent gene expression. Nature, 33, 352355.
  • Thermann, R., Neu-Yilik, G., Deters, A., Frede, U., Wehr, K., Hagemeier, C., Hentze, M.W. & Kulozik, A.E. (1998) Binary specification of nonsense codons by splicing and cytoplasmic translation. EMBO Journal, 17, 34843494.
  • Van der Ploog, L.H.T., Konings, A., Oort, O., Roos, D., Bernini, L.F. & Flavell, R.A. (1980) γβ-thalassemia studies showing that deletion of the γ- and δ-globin genes influences β-globin gene expression in man. Nature, 283, 637642.
  • Volloch, V. & Housman, D. (1981) Stability of globin mRNA in terminally differentiating murine erythroleukemia cells. Cell, 23, 509514.
  • Wang, X., Kiledjian, M., Weiss, I.M. & Liebhaber, S.A. (1995) Detection and characterization of a 3′ untranslated region ribonucleoprotein complex associated with human alpha-globin mRNA stability. Molecular and Cellular Biology, 15, 17691777.
  • Weiss, I.M. & Liebhaber, S.A. (1994) Erythroid cell-specific determinants of alpha-globin mRNA stability. Molecular and Cellular Biology, 14, 81238132.
  • Weiss, I.M. & Liebhaber, S.A. (1995) Erythroid cell-specific mRNA stability elements in the alpha (2)-globin 3′ non-translated region. Molecular and Cellular Biology, 15, 24572465.
  • Wisdom, R. & Lee, W. (1991) The protein coding region of c-myc mRNA contains a sequence that specifies rapid mRNA turnover and induction by protein synthesis inhibitors. Genes and Development, 5, 232243.
  • Yu, J. & Russell, J.E. (2000) Dynamic regulation of globin mRNA stability in β thalassemia. Blood, 96, 2408a.
  • Yu, J. & Russell, J.E. (2001) Structural and functional analysis of an mRNP complex that mediates the high stability of human β-globin mRNA. Molecular and Cellular Biology, 21, 58795888.