Mitochondrial succinate dehydrogenase function is essential for sperm motility and male fertility

Rachel M. Woodhouse; Natalya Frolows; Guoqiang Wang; Azelle Hawdon; Edmund Heng Kin Wong; Linda C. Dansereau; Yingying Su; Liam D. Adair; Elizabeth J. New; Ashleigh M. Philp; Wei Kang Tan; Andrew Philp; Alyson Ashe

iScience (Dec 2022)

Mitochondrial succinate dehydrogenase function is essential for sperm motility and male fertility

Rachel M. Woodhouse,
Natalya Frolows,
Guoqiang Wang,
Azelle Hawdon,
Edmund Heng Kin Wong,
Linda C. Dansereau,
Yingying Su,
Liam D. Adair,
Elizabeth J. New,
Ashleigh M. Philp,
Wei Kang Tan,
Andrew Philp,
Alyson Ashe

Affiliations

Rachel M. Woodhouse: The University of Sydney, School of Life and Environmental Sciences, Sydney, NSW 2006, Australia; Division of Genome Science and Cancer, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT 2601, Australia
Natalya Frolows: The University of Sydney, School of Life and Environmental Sciences, Sydney, NSW 2006, Australia; CSIRO Health and Biosecurity, Sydney, NSW 2113, Australia
Guoqiang Wang: Department of Molecular Biology and Biochemistry, Nelson Biological Laboratories, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA
Azelle Hawdon: The University of Sydney, School of Life and Environmental Sciences, Sydney, NSW 2006, Australia; Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia
Edmund Heng Kin Wong: The University of Sydney, School of Life and Environmental Sciences, Sydney, NSW 2006, Australia
Linda C. Dansereau: Garvan Institute of Medical Research, Sydney, NSW 2010, Australia; St Vincent’s Clinical School, UNSW Medicine, University of NSW, Sydney, NSW 2010, Australia
Yingying Su: Sydney Microscopy and Microanalysis, The University of Sydney, Sydney, NSW 2006, Australia
Liam D. Adair: The University of Sydney, School of Chemistry, Sydney, NSW 2006, Australia; Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, The University of Sydney, Sydney, NSW 2006, Australia
Elizabeth J. New: The University of Sydney, School of Chemistry, Sydney, NSW 2006, Australia; Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, The University of Sydney, Sydney, NSW 2006, Australia
Ashleigh M. Philp: St Vincent’s Clinical School, UNSW Medicine, University of NSW, Sydney, NSW 2010, Australia
Wei Kang Tan: The University of Sydney, School of Life and Environmental Sciences, Sydney, NSW 2006, Australia
Andrew Philp: Centre for Healthy Ageing, Centenary Institute, Missenden Road, Sydney, NSW 2050, Australia; Charles Perkins Centre, Faculty of Medicine and Health, University of Sydney, NSW 2006, Australia
Alyson Ashe: The University of Sydney, School of Life and Environmental Sciences, Sydney, NSW 2006, Australia; Corresponding author

Journal volume & issue: Vol. 25, no. 12
p. 105573

Abstract

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Summary: Mitochondrial health is crucial to sperm quality and male fertility, but the precise role of mitochondria in sperm function remains unclear. SDHA is a component of the succinate dehydrogenase (SDH) complex and plays a critical role in mitochondria. In humans, SDH activity is positively correlated with sperm quality, and mutations in SDHA are associated with Leigh Syndrome. Here we report that the C. elegans SDHA orthologue SDHA-2 is essential for male fertility: sdha-2 mutants produce dramatically fewer offspring due to defective sperm activation and motility, have hyperfused sperm mitochondria, and disrupted redox balance. Similar sperm motility defects in sdha-1 and icl-1 mutant animals suggest an imbalance in metabolites may underlie the fertility defect. Our results demonstrate a role for SDHA-2 in sperm motility and male reproductive health and establish an animal model of SDH deficiency-associated infertility.

Published in iScience

ISSN: 2589-0042 (Online)
Publisher: Elsevier
Country of publisher: United States
LCC subjects: Science
Website: http://www.cell.com/iscience/home

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