Browse by author
Lookup NU author(s): Dr Adrian Watson
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
A subtraction library was prepared from cultures of Aspergillus niger that had or had not been exposed to dithiothreitol (DTT), in order to identify genes involved in the unfolded protein response (UPR) or in the response to reductive stress. A large fraction of the clones in the library (40%) encoded two putative methyltransferases (MTs) whose function has yet to be determined. Other stress-responsive genes included a homologue of the Mn2+ -containing superoxide dismutase gene (sodB) and a number of genes predicted to code for products that function in protein turnover and in intra- and extracellular transport of molecules. Transcriptional microarray analysis was carried out with a group of 15 genes, comprising 11 from the cDNA library, two genes linked to the putative MT genes but not represented in the library, and two UPR control genes (bipA and pdiA). Eleven of the 15 genes were inducible with DTT. This was either reflected by the presence of transcripts in cells subjected to DTT stress compared to absence under control conditions, or by an induction ratio of between 1.4 and 8.0 in cases where transcripts were already detectable under control conditions. The MT genes were among the four most highly induced. None of the genes, apart from bipA and pdiA, showed significant induction in response to other stresses that are known to induce the UPR in fungi. We conclude that DTT alone does not provide for specific induction of UPR genes and that other stress conditions must also be examined. © Springer-Verlag 2005.
Author(s): MacKenzie DA, Guillemette T, Al-Sheikh H, Watson AJ, Jeenes DJ, Wongwathanarat P, Dunn-Coleman NS, Peij NV, Archer DB
Publication type: Article
Publication status: Published
Journal: Molecular Genetics and Genomics
Year: 2005
Volume: 274
Issue: 4
Pages: 410-418
ISSN (print): 1617-4615
ISSN (electronic): 1617-4623
Publisher: Springer
URL: http://dx.doi.org/10.1007/s00438-005-0034-3
DOI: 10.1007/s00438-005-0034-3
PubMed id: 16160852
Altmetrics provided by Altmetric