Literature DB >> 11865046

RNA destabilization by the granulocyte colony-stimulating factor stem-loop destabilizing element involves a single stem-loop that promotes deadenylation.

R A Putland1, T A Sassinis, J S Harvey, P Diamond, L S Coles, C Y Brown, G J Goodall.   

Abstract

Granulocyte colony-stimulating factor (G-CSF) mRNA contains two distinct types of cis-acting mRNA destabilizing elements in the 3'-untranslated region. In addition to several copies of the AU-rich element the G-CSF mRNA also contains a destabilizing region that includes several predicted stem-loop structures. We report here that the destabilizing activity resides in a single stem-loop structure within this region. A consensus sequence for the active structure has been derived by site-directed mutagenesis, revealing that a three-base loop of sequence YAU and unpaired bases either side of the stem contribute to the activity. The helical nature of the stem is essential and the stem must be less than 11 bp in length, but the destabilizing activity is relatively insensitive to the sequence within the helix. The stem-loop increases the rate of mRNA deadenylation, most likely by enhancing the processivity of the deadenylation reaction. A protein that binds the stem-loop, but not an inactive mutant form, has been detected in cytoplasmic lysates.

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Year:  2002        PMID: 11865046      PMCID: PMC135610          DOI: 10.1128/MCB.22.6.1664-1673.2002

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  27 in total

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Authors:  R Binder; S P Hwang; R Ratnasabapathy; D L Williams
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3.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

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Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

4.  Transcriptional and posttranscriptional modulation of myeloid colony-stimulating factor expression by tumor necrosis factor and other agents.

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Journal:  Mol Cell Biol       Date:  1988-08       Impact factor: 4.272

5.  Sequence-specific endonucleolytic cleavage and protection of mRNA in Xenopus and Drosophila.

Authors:  B D Brown; I D Zipkin; R M Harland
Journal:  Genes Dev       Date:  1993-08       Impact factor: 11.361

6.  Molecular cloning and expression of the cDNA encoding feline granulocyte colony-stimulating factor.

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7.  Isolation and characterization of the cDNA for murine granulocyte colony-stimulating factor.

Authors:  M Tsuchiya; S Asano; Y Kaziro; S Nagata
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8.  Regulation of granulocyte- and monocyte-colony stimulating factor mRNA levels in human blood monocytes is mediated primarily at a post-transcriptional level.

Authors:  T J Ernst; A R Ritchie; G D Demetri; J D Griffin
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9.  Poly(A) shortening and degradation of the 3' A+U-rich sequences of human c-myc mRNA in a cell-free system.

Authors:  G Brewer; J Ross
Journal:  Mol Cell Biol       Date:  1988-04       Impact factor: 4.272

10.  Molecular cloning of the chicken myelomonocytic growth factor (cMGF) reveals relationship to interleukin 6 and granulocyte colony stimulating factor.

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  14 in total

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Review 2.  A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants.

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3.  Common variations in noncoding regions of the human natriuretic peptide receptor A gene have quantitative effects.

Authors:  Joshua W Knowles; Laurie M Erickson; Vanessa K Guy; Carlie S Sigel; Jennifer C Wilder; Nobuyo Maeda
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Review 4.  Post-transcriptional regulons coordinate the initiation and resolution of inflammation.

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Review 5.  RNase-L control of cellular mRNAs: roles in biologic functions and mechanisms of substrate targeting.

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7.  Destabilization of interleukin-6 mRNA requires a putative RNA stem-loop structure, an AU-rich element, and the RNA-binding protein AUF1.

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8.  New families of human regulatory RNA structures identified by comparative analysis of vertebrate genomes.

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9.  Identification of new high affinity targets for Roquin based on structural conservation.

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10.  Identification of signaling components required for the prediction of cytokine release in RAW 264.7 macrophages.

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