The protein-coding region of c-myc mRNA contains a sequence that specifies rapid mRNA turnover and induction by protein synthesis inhibitors - PubMed (original) (raw)
The protein-coding region of c-myc mRNA contains a sequence that specifies rapid mRNA turnover and induction by protein synthesis inhibitors
R Wisdom et al. Genes Dev. 1991 Feb.
Free article
Abstract
The stability of certain mRNAs is known to be affected by translation. Some mRNAs appear to be protected from rapid degradation by translation, whereas degradation is coupled to translation for other mRNAs. The molecular determinants of this selective effect of translation are unknown. One example of this effect is the induction of early-response gene mRNAs in the presence of translation inhibitors. To define the molecular basis of induction of early-response gene mRNA expression by inhibitors of protein synthesis, we have performed a mutational analysis of one member of the early response gene family, the c-myc gene. We find that induction by cycloheximide is due to stabilization of c-myc transcripts. The requirements for increased expression of c-myc mRNA by cycloheximide are the presence of the sequence encoding c-myc amino acids 335-439 on a mRNA that can be translated; all other portions of the c-myc gene are dispensable, and this sequence can confer induction of mRNA expression by protein synthesis inhibitors on a heterologous gene. By direct measurement of mRNA turnover in the absence of transcription-blocking drugs, we show that this sequence can function as a selective mRNA destabilizing element, that turnover mediated by this element is translation dependent, and turnover mediated by this element is inhibited by actinomycin D. Our results support the hypothesis that degradation of c-myc mRNA is coupled to translation, that the sequences specifying this form of degradation are contained in the protein-coding sequence, and that translation inhibitors induce expression of c-myc mRNA by blocking turnover mediated by this element.
Similar articles
- c-myc mRNA is down-regulated during myogenic differentiation by accelerated decay that depends on translation of regulatory coding elements.
Yeilding NM, Procopio WN, Rehman MT, Lee WM. Yeilding NM, et al. J Biol Chem. 1998 Jun 19;273(25):15749-57. doi: 10.1074/jbc.273.25.15749. J Biol Chem. 1998. PMID: 9624173 - Translation of c-myc mRNA is required for its post-transcriptional regulation during myogenesis.
Wisdom R, Lee W. Wisdom R, et al. J Biol Chem. 1990 Nov 5;265(31):19015-21. J Biol Chem. 1990. PMID: 2229059 - cis-acting determinants of c-myc mRNA stability.
Cole MD, Mango SE. Cole MD, et al. Enzyme. 1990;44(1-4):167-80. doi: 10.1159/000468755. Enzyme. 1990. PMID: 2133648 - What determines the instability of c-myc proto-oncogene mRNA?
Laird-Offringa IA. Laird-Offringa IA. Bioessays. 1992 Feb;14(2):119-24. doi: 10.1002/bies.950140209. Bioessays. 1992. PMID: 1575711 Review. - Multiple determinants of eukaryotic mRNA stability.
Cleveland DW, Yen TJ. Cleveland DW, et al. New Biol. 1989 Nov;1(2):121-6. New Biol. 1989. PMID: 2518709 Review.
Cited by
- Smg6/Est1 licenses embryonic stem cell differentiation via nonsense-mediated mRNA decay.
Li T, Shi Y, Wang P, Guachalla LM, Sun B, Joerss T, Chen YS, Groth M, Krueger A, Platzer M, Yang YG, Rudolph KL, Wang ZQ. Li T, et al. EMBO J. 2015 Jun 12;34(12):1630-47. doi: 10.15252/embj.201489947. Epub 2015 Mar 14. EMBO J. 2015. PMID: 25770585 Free PMC article. - Mutational inactivation of an inhibitory sequence in human immunodeficiency virus type 1 results in Rev-independent gag expression.
Schwartz S, Campbell M, Nasioulas G, Harrison J, Felber BK, Pavlakis GN. Schwartz S, et al. J Virol. 1992 Dec;66(12):7176-82. doi: 10.1128/JVI.66.12.7176-7182.1992. J Virol. 1992. PMID: 1433510 Free PMC article. - A mutation in the tRNA nucleotidyltransferase gene promotes stabilization of mRNAs in Saccharomyces cerevisiae.
Peltz SW, Donahue JL, Jacobson A. Peltz SW, et al. Mol Cell Biol. 1992 Dec;12(12):5778-84. doi: 10.1128/mcb.12.12.5778-5784.1992. Mol Cell Biol. 1992. PMID: 1448105 Free PMC article. - A constitutive decay element promotes tumor necrosis factor alpha mRNA degradation via an AU-rich element-independent pathway.
Stoecklin G, Lu M, Rattenbacher B, Moroni C. Stoecklin G, et al. Mol Cell Biol. 2003 May;23(10):3506-15. doi: 10.1128/MCB.23.10.3506-3515.2003. Mol Cell Biol. 2003. PMID: 12724409 Free PMC article. - Nucleolin and YB-1 are required for JNK-mediated interleukin-2 mRNA stabilization during T-cell activation.
Chen CY, Gherzi R, Andersen JS, Gaietta G, Jürchott K, Royer HD, Mann M, Karin M. Chen CY, et al. Genes Dev. 2000 May 15;14(10):1236-48. Genes Dev. 2000. PMID: 10817758 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources