The chicken ubiquitin gene contains a heat shock promoter and expresses an unstable mRNA in heat-shocked cells.
Open Access
- 1 December 1986
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 6 (12) , 4602-4610
- https://doi.org/10.1128/mcb.6.12.4602
Abstract
A chicken genomic library was screened to obtain genomic clones for ubiquitin genes. Two genes that differ in their genomic location and organization were identified. One gene, designated Ub I, contains four copies of the protein-coding sequence arranged in tandem, while the second gene, Ub II, contains three. The origin of the two major mRNAs that are induced after heat shock in chicken embryo fibroblasts was determined by generating DNA probes from the 5'-and 3'-noncoding regions of the two genes. Both mRNAs are transcribed from Ub I, the larger being the unspliced precursor of the smaller. A 674-base-pair intron was located within the 5'-noncoding region of Ub I. The second gene, Ub II, does not appear to code for an RNA species in normal or heat-shocked chicken embryo fibroblasts. The expression of ubiquitin mRNA during heat shock and recovery was examined. Addition of actinomycin D before heat shock completely abolished the response of ubiquitin mRNA to the stress. Analysis of the stability of the mRNA during recovery revealed that the mRNA accumulated during the heat shock is rapidly degraded with a half-life of approximately 1.5 h, suggesting a specialized but transient role for ubiquitin during heat shock.This publication has 44 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- RNA splicing is interrupted by heat shock and is rescued by heat shock protein synthesisCell, 1986
- The Heat Shock ResponsCritical Reviews in Biochemistry, 1985
- Formation of conjugates by 125I‐labelled ubiquitin microinjected into cultured hepatoma cellsFEBS Letters, 1982
- Developmentally regulated transcription from Drosophila melanogaster chromosomal site 67BDevelopmental Biology, 1982
- A set of synthetic oligodeoxyribonucleotide primers for DNA sequencing in the plasmid vector pBR322Gene, 1981
- Protein A24 lyase is an isopeptidaseFEBS Letters, 1981
- Protein A24 lyase activity in nucleoli of thioacetamide-treated rat liver releases histone 2A and ubiquitin from conjugated protein A24Biochemistry, 1981
- The use of thin acrylamide gels for DNA sequencingFEBS Letters, 1978
- Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase IJournal of Molecular Biology, 1977