Loss of a 20S Proteasome Activator inSaccharomyces cerevisiaeDownregulates Genes Important for Genomic Integrity, Increases DNA Damage, and Selectively Sensitizes Cells to Agents With Diverse Mechanisms of Action

Author:

Doherty Kevin M12,Pride Leah D13,Lukose James1,Snydsman Brian E4,Charles Ronald1,Pramanik Ajay1,Muller Eric G4,Botstein David5,Moore Carol Wood116

Affiliation:

1. Department of Microbiology and Immunology, City University of New York Sophie Davis School of Biomedical Education, City College, New York, New York 10031-9101

2. The Graduate Center Program in Biochemistry, City University of New York, New York, New York 10016-4309

3. Department of Biochemistry, City College, City University of New York, New York, New York 10031-9101

4. Department of Biochemistry, University of Washington, Seattle, Washington 98195-7350

5. Lewis-Sigler Institute for Integrative Genomics and Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544-1004, and

6. Graduate Center Programs in Biochemistry and Biology, City University of New York, New York, New York 10016-4309

Abstract

AbstractCytoprotective functions of a 20S proteasome activator were investigated. Saccharomyces cerevisiae  Blm10 and human 20S proteasome activator 200 (PA200) are homologs. Comparative genome-wide analyses of untreated diploid cells lacking Blm10 and growing at steady state at defined growth rates revealed downregulation of numerous genes required for accurate chromosome structure, assembly and repair, and upregulation of a specific subset of genes encoding protein-folding chaperones. Blm10 loss or truncation of the Ubp3/Blm3 deubiquitinating enzyme caused massive chromosomal damage and cell death in homozygous diploids after phleomycin treatments, indicating that Blm10 and Ubp3/Blm3 function to stabilize the genome and protect against cell death. Diploids lacking Blm10 also were sensitized to doxorubicin, hydroxyurea, 5-fluorouracil, rapamycin, hydrogen peroxide, methyl methanesulfonate, and calcofluor. Fluorescently tagged Blm10 localized in nuclei, with enhanced fluorescence after DNA replication. After DNA damage that caused a classic G2/M arrest, fluorescence remained diffuse, with evidence of nuclear fragmentation in some cells. Protective functions of Blm10 did not require the carboxyl-terminal region that makes close contact with 20S proteasomes, indicating that protection does not require this contact or the truncated Blm10 can interact with the proteasome apart from this region. Without its carboxyl-terminus, Blm10(−339aa) localized to nuclei in untreated, nonproliferating (G0) cells, but not during G1 S, G2, and M. The results indicate Blm10 functions in protective mechanisms that include the machinery that assures proper assembly of chromosomes. These essential guardian functions have implications for ubiquitin-independent targeting in anticancer therapy. Targeting Blm10/PA200 together with one or more of the upregulated chaperones or a conventional treatment could be efficacious.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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