Insm2 deficiency results in female infertility by disturbing steroid pathway and decreasing ovarian reserve in mice

Cell Cycle. 2022 Nov;21(21):2255-2267. doi: 10.1080/15384101.2022.2092816. Epub 2022 Jul 3.

Abstract

The number and quality of oocytes in the ovarian reserve are related to fertility and reproductive lifespan in mammals. Some transcription factors have been demonstrated to determine oogenesis. The insulinoma-associated 2 (Insm2) gene is a member of the Snail transcriptional repressor superfamily. Recent studies have demonstrated Insm2 plays an essential role for insulin secretion and glucose intolerance in mice, but the functions of Insm2 in reproduction remain elusive. Here, by examination of Insm2 knockout mice, we found Insm2 was essential for female fertility. Loss of Insm2 resulted in female infertility with major defects in primordial follicle pool, ovarian folliculogenesis and ovulation. Transcriptomic profiling of ovaries suggests that loss of Insm2 caused defects in oocyte meiosis and steroid synthesis. Both oocyte- and granulosa cell-expressed genes were dysregulated, including Foxo1 and other known genes involved in primary ovarian insufficiency. Together, these studies show that Insm2 is required for oocyte development and their communication with ovarian somatic cells.

Keywords: Insm2; infertility; steroid synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Female
  • Infertility, Female* / genetics
  • Mammals
  • Mice
  • Mice, Knockout
  • Oocytes / metabolism
  • Ovarian Reserve*
  • Steroids
  • Transcription Factors / metabolism

Substances

  • Steroids
  • Transcription Factors

Grants and funding

This work was supported by the National Key R&D Program of China [2018YFC1004001, 2018YFC1004502]; National Natural Science Foundation of China [NSFC 31771661]; Fundamental Research Funds for the Central Universities [2019kfyXKJC074].