Mitochondrial E3 ubiquitin ligase MARCH5 is required for mouse oocyte meiotic maturation

Author:

Zhou Qian123,Xu Ke1,Zhao Bing-Wang1,Qiao Jing-Yi1,Li Yuan-Yuan1,Lei Wen-Long1,Li Jian4,Ouyang Ying-Chun1,Hou Yi1,Schatten Heide5,Wang Zhen-Bo1,Sun Qing-Yuan6

Affiliation:

1. State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences , Beijing , China

2. International Cancer Center, Shenzhen University Medical School , Shenzhen , China

3. Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences , Shenzhen , China

4. Department of Reproductive Medicine, Peking University Shenzhen Hospital , Shenzhen , China

5. Department of Veterinary Pathobiology, University of Missouri , Columbia, MO , USA

6. Fertility Preservation Lab, Guangdong-Hong Kong Metabolism & Reproduction Joint Laboratory, Reproductive Medicine Center, Guangdong Second Provincial General Hospital , Guangzhou , China

Abstract

AbstractAs the most abundant organelles in oocytes, mitochondria play an important role in maintaining oocyte quality. Here, we report that March5, encoding a mitochondrial ubiquitin ligase that promotes mitochondrial elongation, plays a critical role in mouse oocyte meiotic maturation via regulating mitochondrial function. The subcellular localization of MARCH5 was similar to the mitochondrial distribution during mouse oocyte meiotic progression. Knockdown of March5 caused decreased ratios of the first polar body extrusion. March5-siRNA injection resulted in oocyte mitochondrial dysfunctions, manifested by increased reactive oxygen species, decreased ATP content as well as decreased mitochondrial membrane potential, leading to reduced ability of spindle formation and an increased ratio of kinetochore–microtubule detachment. Further study showed that the continuous activation of the spindle assembly checkpoint and the failure of Cyclin B1 degradation caused MI arrest and first polar body (PB1) extrusion failure in March5 knockdown oocytes. Taken together, our results demonstrated that March5 plays an essential role in mouse oocyte meiotic maturation, possibly via regulation of mitochondrial function and/or ubiquitination of microtubule dynamics- or cell cycle-regulating proteins.

Funder

CAS Special Research Assistant Program

China Postdoctoral Science Foundation General Project

Shenzhen Science and Technology Program

Natural Science Foundation of Shandong Province

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,General Medicine,Reproductive Medicine

Reference32 articles.

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