Characterization of adapt33, a Stress-Inducible Riboregulator

• Published in: Gene expression 2003-01, Vol.11 (2), p.85-94
• Main Authors: WANG, YANHONG, DAVIES, KELVIN J. A., MELENDEZ, J. ANDRES, CRAWFORD, DANA R.
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents - pharmacology; Apoptosis; Apoptosis - drug effects; Cell culture; Chloramphenicol O-Acetyltransferase - metabolism; CHO Cells; Cisplatin - pharmacology; Cloning; Cricetinae; DNA Primers - genetics; DNA, Complementary - genetics; Enzyme Inhibitors - pharmacology; Genes; Humans; Hybridization; Hydrogen peroxide; Hydrogen Peroxide - pharmacology; mRNA stability; Ovaries; Oxidants; Oxidants - pharmacology; Oxidative Stress - genetics; Oxidizing agents; Promoter Regions, Genetic - genetics; Proteins; Ribonucleic acid; Riboregulator Adaptive Response Gene Expression Hydrogen Peroxide Oxidative Stress Hamster Fibroblasts; RNA; RNA polymerase; RNA, Messenger - genetics; RNA, Messenger - metabolism; Stability; Staurosporine; Staurosporine - pharmacology; Transcription, Genetic
• ISSN: 1052-2166; 1555-3884
• DOI: 10.3727/000000003108748982

We have identified adapt33 as a multiple stress-responsive gene that is induced under conditions of a cytoprotective "adaptive response." adapt33 RNA does not contain any appreciable open reading frame nor produce a protein product and is therefore classified as a stress-inducible riboregulator. Although a number of oxidant stress-modulated, protein-encoding genes have been reported and characterized, very few stress-inducible riboregulator RNAs are known. Here we extend previous studies toward understanding the underlying regulation of expression and function of this rare mammalian riboregulator. mRNA stability and transcription studies determined that adapt33 induction by hydrogen peroxide is at the mRNA stability level, and that adapt33 has a very short half-life. Surprisingly, adapt33 mRNA also exhibits altered electrophoretic migration in response to both hydrogen peroxide and cis-platinum treatment. Although no transcriptional modulation in response to hydrogen peroxide was observed, fusion promoter constructs revealed that adapt33 has an unusually strong promoter that is active in both hamster and human cells. Analysis of expression following the stimulation of apoptosis with hydrogen peroxide and staurosporine revealed a strong correlation with apoptosis, suggesting a possible novel, noncoding RNA component of the apoptotic mechanism. We conclude that adapt33 is a stress-inducible, apoptosis-associated RNA with unique structural and gene promoter characteristics.