Oocyte mitochondria link maternal environment to offspring phenotype.
Jason F CooperKim NguyenDarrick GatesEmily WolfrumColt CapanHyoungjoo LeeDevia WilliamsChidozie OkoyeAndrew P WojtovichNicholas O BurtonPublished in: Research square (2024)
During maturation oocytes undergo a recently discovered mitochondrial proteome remodeling event in flies 1 , frogs 1 , and humans 2 . This oocyte mitochondrial remodeling, which includes substantial changes in electron transport chain (ETC) subunit abundance 1,2 , is regulated by maternal insulin signaling 1 . Why oocytes undergo mitochondrial remodeling is unknown, with some speculating that it might be an evolutionarily conserved mechanism to protect oocytes from genotoxic damage by reactive oxygen species (ROS) 2 . In Caenorhabditis elegans , we previously found that maternal exposure to osmotic stress drives a 50-fold increase in offspring survival in response to future osmotic stress 3 . Like mitochondrial remodeling, we found that this intergenerational adaptation is also regulated by insulin signaling to oocytes 3 . Here, we used proteomics and genetic manipulations to show that insulin signaling to oocytes regulates offspring's ability to adapt to future stress via a mechanism that depends on ETC composition in maternal oocytes. Specifically, we found that maternally expressed mutant alleles of nduf-7 (complex I subunit) or isp-1 (complex III subunit) altered offspring's response to osmotic stress at hatching independently of offspring genotype. Furthermore, we found that expressing wild-type isp-1 in germ cells (oocytes) was sufficient to restore offspring's normal response to osmotic stress. Chemical mutagenesis screens revealed that maternal ETC composition regulates offspring's response to stress by altering AMP kinase function in offspring which in turn regulates both ATP and glycerol metabolism in response to continued osmotic stress. To our knowledge, these data are the first to show that proper oocyte ETC composition is required to link a mother's environment to adaptive changes in offspring metabolism. The data also raise the possibility that the reason diverse animals exhibit insulin regulated remodeling of oocyte mitochondria is to tailor offspring metabolism to best match the environment of their mother.
Keyphrases
- high fat diet
- type diabetes
- reactive oxygen species
- oxidative stress
- stress induced
- birth weight
- wild type
- adipose tissue
- cell death
- pregnancy outcomes
- insulin resistance
- healthcare
- gene expression
- electronic health record
- genome wide
- crispr cas
- heat stress
- skeletal muscle
- cell proliferation
- wastewater treatment
- cell cycle arrest
- quantum dots
- copy number
- embryonic stem cells