Genes Required for Survival in Microgravity Revealed by Genome-Wide Yeast Deletion Collections Cultured during Spaceflight

Author:

Nislow Corey1,Lee Anna Y.2,Allen Patricia L.3,Giaever Guri1,Smith Andrew2,Gebbia Marinella2,Stodieck Louis S.4,Hammond Jeffrey S.5,Birdsall Holly H.67,Hammond Timothy G.3689

Affiliation:

1. Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, BC, Canada V6T 1Z3

2. Donnelly CCBR, University of Toronto, Toronto, ON, Canada M5S 3E1

3. Durham VA Medical Center, Research & Development Service, Durham, NC 27705, USA

4. Bioserve Space Technologies, University of Colorado, Boulder, CO 80309, USA

5. The Institute for Medical Research, Durham, NC 27705, USA

6. Department of Veterans Affairs Office of Research and Development, Washington, DC 20420, USA

7. Departments of Otorhinolaryngology, Immunology, and Psychiatry, Baylor College of Medicine, Houston, TX 77030, USA

8. Nephrology Division, Department of Internal Medicine, Duke University School of Medicine, Durham, NC 27705, USA

9. Nephrology Section, Department of Internal Medicine, George Washington University School of Medicine, Washington, DC 20052, USA

Abstract

Spaceflight is a unique environment with profound effects on biological systems including tissue redistribution and musculoskeletal stresses. However, the more subtle biological effects of spaceflight on cells and organisms are difficult to measure in a systematic, unbiased manner. Here we test the utility of the molecularly barcoded yeast deletion collection to provide a quantitative assessment of the effects of microgravity on a model organism. We developed robust hardware to screen, in parallel, the complete collection of ~4800 homozygous and ~5900 heterozygous (including ~1100 single-copy deletions of essential genes) yeast deletion strains, each carrying unique DNA that acts as strain identifiers. We compared strain fitness for the homozygous and heterozygous yeast deletion collections grown in spaceflight and ground, as well as plus and minus hyperosmolar sodium chloride, providing a second additive stressor. The genome-wide sensitivity profiles obtained from these treatments were then queried for their similarity to a compendium of drugs whose effects on the yeast collection have been previously reported. We found that the effects of spaceflight have high concordance with the effects of DNA-damaging agents and changes in redox state, suggesting mechanisms by which spaceflight may negatively affect cell fitness.

Funder

National Aeronautics and Space Administration

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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