Previous Article | Next Article 
Molecular and Cellular Biology, June 2005, p. 4662-4675, Vol. 25, No. 11
0270-7306/05/$08.00+0 doi:10.1128/MCB.25.11.4662-4675.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Identification and Characterization of a Drosophila Proteasome Regulatory Network
Josefin Lundgren,
Patrick Masson,
Zahra Mirzaei, and
Patrick Young*
Department of Molecular Biology and Functional Genomics, Stockholm University, S-10691 StockholmSweden
Received 31 March 2004/
Returned for modification 17 May 2004/
Accepted 28 February 2005
Maintaining adequate proteasomal proteolytic activity is essential for eukaryotic cells. For metazoan cells, little is known about the composition of genes that are regulated in the proteasome network or the mechanisms that modulate the levels of proteasome genes. Previously, two distinct treatments have been observed to induce 26S proteasome levels in Drosophila melanogaster cell lines, RNA interference (RNAi)-mediated inhibition of the 26S proteasome subunit Rpn10/S5a and suppression of proteasome activity through treatment with active-site inhibitors. We have carried out genome array profiles from cells with decreased Rpn10/S5a levels using RNAi or from cells treated with proteasome inhibitor MG132 and have thereby identified candidate genes that are regulated as part of a metazoan proteasome network. The profiles reveal that the majority of genes that were identified to be under the control of the regulatory network consisted of 26S proteasome subunits. The 26S proteasome genes, including three new subunits, Ubp6p, Uch-L3, and Sem1p, were found to be up-regulated. A number of genes known to have proteasome-related functions, including Rad23, isopeptidase T, sequestosome, and the genes for the segregase complex TER94/VCP-Ufd1-Npl4 were also found to be up-regulated. RNAi-mediated inhibition against the segregase complex genes demonstrated pronounced stabilization of proteasome substrates throughout the Drosophila cell. Finally, transcriptional reporter assays and deletion mapping studies in Drosophila demonstrate that proteasome mRNA induction is dependent upon the 5' untranslated regions (UTRs). Transfer of the 5' UTR from the proteasome subunit Rpn1/S2 to a noninducible promoter was sufficient to confer transcriptional upregulation of the reporter mRNA after proteasome inhibition.
* Corresponding author. Mailing address: Department of Molecular Biology and Functional Genomics, Stockholm University, S-106 91 Stockholm, Sweden. Phone: 46-8-164135. Fax: 46-8-152350. E-mail:
patrick.young{at}molbio.su.se.
Supplemental material for this article may be found at http://mcb.asm.org/.
Molecular and Cellular Biology, June 2005, p. 4662-4675, Vol. 25, No. 11
0022-538X/05/$08.00+0 doi:10.1128/MCB.25.11.4662-4675.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Dantuma, N. P., Lindsten, K.
(2009). Stressing the ubiquitin/proteasome system. Cardiovasc Res
0: cvp255v2-cvp255
[Abstract]
[Full Text]
-
Wiseman, R. L., Chin, K.-T., Haynes, C. M., Stanhill, A., Xu, C.-F., Roguev, A., Krogan, N. J., Neubert, T. A., Ron, D.
(2009). Thioredoxin-related Protein 32 Is an Arsenite-regulated Thiol Reductase of the Proteasome 19 S Particle. J. Biol. Chem.
284: 15233-15245
[Abstract]
[Full Text]
-
Andersen, K. M., Madsen, L., Prag, S., Johnsen, A. H., Semple, C. A., Hendil, K. B., Hartmann-Petersen, R.
(2009). Thioredoxin Txnl1/TRP32 Is a Redox-active Cofactor of the 26 S Proteasome. J. Biol. Chem.
284: 15246-15254
[Abstract]
[Full Text]
-
Bianchi, G., Oliva, L., Cascio, P., Pengo, N., Fontana, F., Cerruti, F., Orsi, A., Pasqualetto, E., Mezghrani, A., Calbi, V., Palladini, G., Giuliani, N., Anderson, K. C., Sitia, R., Cenci, S.
(2009). The proteasome load versus capacity balance determines apoptotic sensitivity of multiple myeloma cells to proteasome inhibition. Blood
113: 3040-3049
[Abstract]
[Full Text]
-
Bedford, L., Hay, D., Devoy, A., Paine, S., Powe, D. G., Seth, R., Gray, T., Topham, I., Fone, K., Rezvani, N., Mee, M., Soane, T., Layfield, R., Sheppard, P. W., Ebendal, T., Usoskin, D., Lowe, J., Mayer, R. J.
(2008). Depletion of 26S Proteasomes in Mouse Brain Neurons Causes Neurodegeneration and Lewy-Like Inclusions Resembling Human Pale Bodies. J. Neurosci.
28: 8189-8198
[Abstract]
[Full Text]
-
Hoopfer, E. D., Penton, A., Watts, R. J., Luo, L.
(2008). Genomic Analysis of Drosophila Neuronal Remodeling: A Role for the RNA-Binding Protein Boule as a Negative Regulator of Axon Pruning. J. Neurosci.
28: 6092-6103
[Abstract]
[Full Text]
-
Wojtczak, A., Kwiatkowska, M.
(2008). Immunocytochemical and Ultrastructural Analyses of the Function of the Ubiquitin-Proteasome System During Spermiogenesis with the Use of the Inhibitors of Proteasome Proteolytic Activity in the Alga, Chara vulgaris. Biol. Reprod.
78: 577-585
[Abstract]
[Full Text]
-
Moreno-Moreno, O., Torras-Llort, M., Azorin, F.
(2006). Proteolysis restricts localization of CID, the centromere-specific histone H3 variant of Drosophila, to centromeres. Nucleic Acids Res
34: 6247-6255
[Abstract]
[Full Text]