Mitochondrial endonuclease G mediates breakdown of paternal mitochondria upon fertilization

Author:

Zhou Qinghua1,Li Haimin1,Li Hanzeng12,Nakagawa Akihisa1,Lin Jason L. J.3,Lee Eui-Seung1,Harry Brian L.14,Skeen-Gaar Riley Robert1,Suehiro Yuji5,William Donna6,Mitani Shohei5,Yuan Hanna S.3,Kang Byung-Ho7,Xue Ding1

Affiliation:

1. Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.

2. Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA.

3. Institute of Molecular Biology, Academia Sinica, Taipei 11529, Taiwan.

4. Medical Scientist Training Program, University of Colorado, Aurora, CO 80045, USA.

5. Department of Physiology, Tokyo Women’s Medical University, School of Medicine and CREST, Japan Science and Technology Agency, Tokyo 162-8666, Japan.

6. Department of Microbiology and Cell Science, University of Florida, Gainesville, FL 32611, USA.

7. School of Life Sciences, Centre for Cell and Developmental Biology and State Key Laboratory of Agrobiotechnology, Chinese University of Hong Kong, Hong Kong, China.

Abstract

Eliminating paternal mitochondria During fertilization, the oocyte and sperm each bring their mitochondria to the union. Shortly afterward, the paternal mitochondria are degraded, and only the maternal mitochondria are conveyed to the progeny. Zhou et al. observed that the integrity of the inner membrane of paternal mitochondria is compromised, which apparently marks them for degradation (see the Perspective by van der Bliek). Autophagy commences by mitochondrial endonuclease G relocating from the intermembrane space into the matrix and subsequently degrading the paternal mitochondrial DNA. Any delay in this process increases embryonic lethality. Science , this issue p. 394 ; see also p. 351

Funder

March of Dimes

NIH

Research Grants Council of Hong Kong

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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