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AU-rich sequence motifs (specifically sequences containing reiterations of AUUUA) are found in the 3'' untranslated region of mammalian mRNAs encoding cytokines, adhesion molecules, and protooncogenes. Because these AU-rich elements (3''AURE) have been observed to reduce the stability and translational efficiency of transcripts that contain them, and because many of these transcripts accumulate in cells exposed to inflammatory stimuli, we reasoned that mRNAs with 3''AURE may be highly conserved and that the AURE is a marker of mRNAs that are inducible by environmental stressors. To test this hypothesis, we developed a polymerase chain reaction (PCR) strategy to isolate specifically mRNAs with 3''AURE. We first validated the effectiveness of this approach by selectively amplifying two mRNAs containing 3''AURE from interleukin 1 (IL-1)-induced human endothelial cells, then used the same primers in reverse transcriptase-PCR of sea urchin RNA, and used the radiolabeled reaction products to screen a cDNA library prepared from endotoxin-exposed sea urchin coelomocytes. We identified 124 positive clones and isolated a 1608-base-pair fragment that contains an AU-rich consensus sequence upstream from a poly(A) tail. This sea urchin transcript hybridizes with immobilized poly(A)(+)-selected RNA prepared from living coelomocytes maintained in vitro for 8.5-13 h but not with RNA prepared from freshly harvested coelomocytes. Our results provide support for the growing body of evidence that 3'' AURE are both conserved and functional and indicate further that isolation and short-term in vitro culture of sea urchin coelomocytes is sufficient to induce the expression of transcripts containing 3''AURE.
Ando,
Molecular cloning, sequencing, and characterization of cDNA for sarcotoxin IIA, an inducible antibacterial protein of Sarcophaga peregrina (flesh fly).
1988, Pubmed
Ando,
Molecular cloning, sequencing, and characterization of cDNA for sarcotoxin IIA, an inducible antibacterial protein of Sarcophaga peregrina (flesh fly).
1988,
Pubmed
Anisowicz,
Constitutive overexpression of a growth-regulated gene in transformed Chinese hamster and human cells.
1987,
Pubmed
Bagby,
Interleukin-1 stimulation stabilizes GM-CSF mRNA in human vascular endothelial cells: preliminary studies on the role of the 3' AU rich motif.
1990,
Pubmed
Beck,
Isolation and characterization of a primitive interleukin-1-like protein from an invertebrate, Asterias forbesi.
1986,
Pubmed
,
Echinobase
Beck,
Invertebrate cytokines: the phylogenetic emergence of interleukin-1.
1989,
Pubmed
Beutler,
Assay of a ribonuclease that preferentially hydrolyses mRNAs containing cytokine-derived UA-rich instability sequences.
1988,
Pubmed
Bohjanen,
An inducible cytoplasmic factor (AU-B) binds selectively to AUUUA multimers in the 3' untranslated region of lymphokine mRNA.
1991,
Pubmed
Brewer,
An A + U-rich element RNA-binding factor regulates c-myc mRNA stability in vitro.
1991,
Pubmed
Caput,
Identification of a common nucleotide sequence in the 3'-untranslated region of mRNA molecules specifying inflammatory mediators.
1986,
Pubmed
Dorssers,
Characterization of a human multilineage-colony-stimulating factor cDNA clone identified by a conserved noncoding sequence in mouse interleukin-3.
1987,
Pubmed
Fickett,
Recognition of protein coding regions in DNA sequences.
1982,
Pubmed
Gaugitsch,
A novel transiently expressed, integral membrane protein linked to cell activation. Molecular cloning via the rapid degradation signal AUUUA.
1992,
Pubmed
Gillis,
The adenosine-uridine binding factor recognizes the AU-rich elements of cytokine, lymphokine, and oncogene mRNAs.
1991,
Pubmed
Han,
Endotoxin-responsive sequences control cachectin/tumor necrosis factor biosynthesis at the translational level.
1990,
Pubmed
Jones,
Rapid cytoplasmic turnover of c-myc mRNA: requirement of the 3' untranslated sequences.
1987,
Pubmed
Kabnick,
Determinants that contribute to cytoplasmic stability of human c-fos and beta-globin mRNAs are located at several sites in each mRNA.
1988,
Pubmed
Lee,
Sea urchin actin gene subtypes. Gene number, linkage and evolution.
1984,
Pubmed
,
Echinobase
Nakanishi,
DNA homology between the 3'-untranslated regions of a developmentally regulated Drosophila gene and a mouse alpha-interferon gene.
1986,
Pubmed
Nishida,
cDNA cloning of IL-1 alpha and IL-1 beta from mRNA of U937 cell line.
1987,
Pubmed
Rosen,
Optimizing the northern blot procedure.
1990,
Pubmed
Schowalter,
The generation of radiolabeled DNA and RNA probes with polymerase chain reaction.
1989,
Pubmed
Schuler,
GM-CSF and oncogene mRNA stabilities are independently regulated in trans in a mouse monocytic tumor.
1988,
Pubmed
Segal,
Erythroid burst-promoting activity produced by interleukin-1-stimulated endothelial cells is granulocyte-macrophage colony-stimulating factor.
1988,
Pubmed
Shaw,
A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation.
1986,
Pubmed
Stoeckle,
Processing of 9E3 mRNA and regulation of its stability in normal and Rous sarcoma virus-transformed cells.
1989,
Pubmed
Tonouchi,
Deletion of 3' untranslated region of human BSF-2 mRNA causes stabilization of the mRNA and high-level expression in mouse NIH3T3 cells.
1989,
Pubmed
Vakalopoulou,
A 32-kilodalton protein binds to AU-rich domains in the 3' untranslated regions of rapidly degraded mRNAs.
1991,
Pubmed
Virca,
Simplified northern blot hybridization using 5% sodium dodecyl sulfate.
1990,
Pubmed
Vogeli,
Recombinant DNA techniques: storage and screening of cDNA libraries with large numbers of individual colonies from initial transformations.
1985,
Pubmed
Wreschner,
Differential mRNA stability to reticulocyte ribonucleases correlates with 3' non-coding (U)nA sequences.
1988,
Pubmed
Xie,
Expression of a mitogen-responsive gene encoding prostaglandin synthase is regulated by mRNA splicing.
1991,
Pubmed