4.5 Article

Developmental epigenetic programming of adult germ cell death disease: Polycomb protein EZH2-miR-101 pathway

Journal

EPIGENOMICS
Volume 8, Issue 11, Pages 1459-1479

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/epi-2016-0061

Keywords

endocrine-disrupting chemicals; epigenetic programming; male infertility; miRNAs; non-communicable diseases; Polycomb proteins EZH2

Funding

  1. Institut National de la Sante et de la Recherche Medicale (INSERM) [U1065]
  2. University Nice-Sophia-Antipolis
  3. Association Nationale de la Recherche et de la Technologie (ANRT)
  4. BASF Agro (CIFRE)
  5. Long-Range Research Initiative Programme of the European Chemical Industry Council (CEFIC-LRI)
  6. BASF Agro
  7. Agence Nationale de la Recherche (ANR [ANR-06-SEST-13]
  8. Programme National de Recherche en Alimentation (PNRA) [ANR-07-PNRA-016]
  9. Programme National de Recherche sur les Perturbateurs Endocriniens (PNRPE) [PNRPE-2009-12]
  10. Nord Pas-de-Calais region [SER-2007]
  11. Ministere l'Ecologie, du Developpement durable, des Transports et du Logement (MEDDTL) [11-MRES-PNRPE-1-CVS-027 2011]

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Aim: The Developmental Origin of Health and Disease refers to the concept that early exposure to toxicants or nutritional imbalances during perinatal life induces changes that enhance the risk of developing noncommunicable diseases in adulthood. Patients/materials & methods: An experimental model with an adult chronic germ cell death phenotype resulting from exposure to a xenoestrogen was used. Results: A reciprocal negative feedback loop involving decreased EZH2 protein level and increased miR-101 expression was identified. In vitro and in vivo knockdown of EZH2 induced an apoptotic process in germ cells through increased levels of apoptotic factors (BIM and BAD) and DNA repair alteration via topoisomerase 2B deregulation. The increased miR-101 levels were observed in the animal blood, meaning that miR-101 may be a part of a circulating mark of germ cell death. Conclusion: miR-101-EZH2 pathway deregulation could represent a novel pathophysiological epigenetic basis for adult germ cell disease with environmental and developmental origins.

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