Two distinct destabilizing elements in the c-fos message trigger deadenylation as a first step in rapid mRNA decay.

The mechanisms by which c-fos mRNA is targeted for decay have been examined. Rapid removal of the poly(A) tail occurs before the transcribed portion of the c-fos message is degraded. Identification of the determinants that mediate c-fos message deadenylation reveals that they coincide directly with previously characterized determinants of c-fos mRNA instability, one in the protein-coding region and the other an AU-rich element (ARE) in the 3'-untranslated region. Insertion of either of these c-fos instability elements into the stable beta-globin message confers the property of rapid deadenylation. Mutation of the ARE indicates that this sequence controls two steps in the process of c-fos mRNA degradation: removal of the poly(A) tail, which does not require intact AUUUA pentanucleotides within the ARE, and subsequent degradation of the transcribed portion of the message, which appears to be dependent on the AUUUA pentanucleotides. These results indicate that structurally distinct instability determinants within the transcribed portion of labile messages can function by promoting rapid removal of the poly(A) tail as a first step in the decay process.

[1]  R. Jackson,et al.  Do the poly(A) tail and 3′ untranslated region control mRNA translation? , 1990, Cell.

[2]  M. Greenberg,et al.  The regulation and function of c-fos and other immediate early genes in the nervous system , 1990, Neuron.

[3]  Ronald W. Davis,et al.  The poly(A) binding protein is required for poly(A) shortening and 60S ribosomal subunit-dependent translation initiation , 1989, Cell.

[4]  P. Bernstein,et al.  Poly(A), poly(A) binding protein and the regulation of mRNA stability. , 1989, Trends in biochemical sciences.

[5]  S. Peltz,et al.  The poly(A)-poly(A)-binding protein complex is a major determinant of mRNA stability in vitro , 1989, Molecular and cellular biology.

[6]  J. Belasco,et al.  Mechanisms of mRNA decay in bacteria: a perspective. , 1988, Gene.

[7]  Richard Treisman,et al.  Removal of poly(A) and consequent degradation of c-fos mRNA facilitated by 3′ AU-rich sequences , 1988, Nature.

[8]  D. Housman,et al.  Determinants that contribute to cytoplasmic stability of human c-fos and beta-globin mRNAs are located at several sites in each mRNA , 1988, Molecular and cellular biology.

[9]  A. Jacobson,et al.  Determinants of mRNA stability in Dictyostelium discoideum amoebae: differences in poly(A) tail length, ribosome loading, and mRNA size cannot account for the heterogeneity of mRNA decay rates , 1988, Molecular and cellular biology.

[10]  R. Bravo,et al.  Complexity of the early genetic response to growth factors in mouse fibroblasts , 1988, Molecular and cellular biology.

[11]  B. Larkins,et al.  Role of the 3'-poly(A) sequence in translational regulation of mRNAs in Xenopus laevis oocytes. , 1988, The Journal of biological chemistry.

[12]  A. Schönthal,et al.  Posttranscriptional regulation of c-fos mRNA expression. , 1987, Nucleic acids research.

[13]  G. Brawerman Determinants of messenger RNA stability , 1987, Cell.

[14]  G. Shaw,et al.  A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradation , 1986, Cell.

[15]  B. Beutler,et al.  Identification of a common nucleotide sequence in the 3'-untranslated region of mRNA molecules specifying inflammatory mediators. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[16]  L. Lau,et al.  Identification of a set of genes expressed during the G0/G1 transition of cultured mouse cells. , 1985, The EMBO journal.

[17]  T. Curran,et al.  Removal of a 67-base-pair sequence in the noncoding region of protooncogene fos converts it to a transforming gene. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[18]  G. Brawerman,et al.  Regulation of messenger RNA stability in mouse erythroleukemia cells. , 1985, Journal of molecular biology.

[19]  Michael E. Greenberg,et al.  Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogene , 1984, Nature.

[20]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[21]  R. Kornberg,et al.  Repeating structure of cytoplasmic poly(A)-ribonucleoprotein. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[22]  H. Soreq,et al.  Does 3'-terminal poly(A) stabilize human fibroblast interferon mRNA in oocytes of Xenopus laevis? , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[23]  A. Burny,et al.  Absence of polyadenylate segment in globin messenger RNA accelerates its degradation in Xenopus oocytes. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[24]  M. Greenberg,et al.  The c-fos transcript is targeted for rapid decay by two distinct mRNA degradation pathways. , 1989, Genes & development.

[25]  J. Kates Transcription of the Vaccinia Virus Genome and the Occurrence of Polyriboadenylic Acid Sequences in Messenger RNA , 1970 .