4.8 Article

Maintenance of quiescent oocytes by noradrenergic signals

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-021-26945-x

Keywords

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Funding

  1. NIH [P40 OD010440]
  2. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Education [2017R1D1A1B03036182]
  3. Korea Institute of Toxicology [KK-2011-03]
  4. National Research Foundation of Korea (NRF) [2021R1F1A1045599]
  5. JSPS KAKENHI [JP18H02448]
  6. CREST Japan Science and Technology Agency (JST) [JPMJCR1753]
  7. Virginia Commonwealth University
  8. Nagoya University
  9. Inha University
  10. National Research Foundation of Korea [2017R1D1A1B03036182, 2021R1F1A1045599] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Kim et al. demonstrate that octopamine and norepinephrine play a crucial role in maintaining oocyte quiescence across different species, revealing an evolutionarily conserved function of noradrenergic signaling in this process.
Kim et al. show noradrenergic signaling for stress responses such as flight and fight, also serves as a conserved signal for maintaining oocyte quiescence under unfavorable conditions in worms, flies, and fish. All females adopt an evolutionary conserved reproduction strategy; under unfavorable conditions such as scarcity of food or mates, oocytes remain quiescent. However, the signals to maintain oocyte quiescence are largely unknown. Here, we report that in four different species - Caenorhabditis elegans, Caenorhabditis remanei, Drosophila melanogaster, and Danio rerio - octopamine and norepinephrine play an essential role in maintaining oocyte quiescence. In the absence of mates, the oocytes of Caenorhabditis mutants lacking octopamine signaling fail to remain quiescent, but continue to divide and become polyploid. Upon starvation, the egg chambers of D. melanogaster mutants lacking octopamine signaling fail to remain at the previtellogenic stage, but grow to full-grown egg chambers. Upon starvation, D. rerio lacking norepinephrine fails to maintain a quiescent primordial follicle and activates an excessive number of primordial follicles. Our study reveals an evolutionarily conserved function of the noradrenergic signal in maintaining quiescent oocytes.

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