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Mitofusin 2 plays a role in oocyte and follicle development, and is required to maintain ovarian follicular reserve during reproductive aging
Author(s) -
Man Zhang,
Muhammed Burak Bener,
Zongliang Jiang,
Tianren Wang,
Ecem Esencan,
Richard Scott,
Tamas L. Horváth,
Emre Seli
Publication year - 2019
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102024
Subject(s) - mfn2 , oocyte , follicular phase , ovarian follicle , mitochondrial fusion , microbiology and biotechnology , biology , ovarian reserve , andrology , mitochondrion , folliculogenesis , medicine , endocrinology , mitochondrial dna , embryo , genetics , embryogenesis , pregnancy , gene , infertility
Mitochondria change their shape through fusion and fission in order to adapt to their metabolic milieu. Mitofusin-2 (MFN2) is a key regulatory protein in this process, mediating mitochondrial fusion and interaction with endoplasmic reticulum. Targeted deletion of Mfn2 in oocytes resulted in mitochondrial dysfunction and female subfertility associated with impaired oocyte maturation and follicle development. Oocytes lacking MFN2 showed shortened telomeres and increased apoptosis, resulting in compromised oocyte quality and accelerated follicular depletion, consistent with a reproductive aging phenotype.

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