Human Bcl-2 Reverses Survival Defects in Yeast Lacking Superoxide Dismutase and Delays Death of Wild-Type Yeast

Author:

Longo Valter D.1,Ellerby Lisa M.1,Bredesen Dale E.11,Valentine Joan S.1,Gralla Edith B.1

Affiliation:

1. Department of Chemistry and Biochemistry, University of California at Los Angeles, Los Angeles, California 90095-1569; Program on Aging, The Burnham Institute, La Jolla, California 92037; and Neuroscience Department, University of California at San Diego, La Jolla, California 92093

Abstract

We expressed the human anti-apoptotic protein, Bcl-2, in Saccharomyces cerevisiae to investigate its effects on antioxidant protection and stationary phase survival. Yeast lacking copper-zinc superoxide dismutase (sod1Δ) show a profound defect in entry into and survival during stationary phase even under conditions optimal for survival of wild-type strains (incubation in water after stationary phase is reached). Expression of Bcl-2 in the sod1Δ strain caused a large improvement in viability at entry into stationary phase, as well as increased resistance to 100% oxygen and increased catalase activity. In addition, Bcl-2 expression reduced mutation frequency in both wild-type and sod1Δ strains. In another set of experiments, wild-type yeast incubated in expired minimal medium instead of water lost viability quickly; expression of Bcl-2 significantly delayed this stationary phase death. Our results demonstrate that Bcl-2 has activities in yeast that are similar to activities it is known to possess in mammalian cells: (a) stimulation of antioxidant protection and (b) delay of processes leading to cell death.

Publisher

Rockefeller University Press

Subject

Cell Biology

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