piRNA-associated proteins and retrotransposons are differentially expressed in murine testis and ovary of aryl hydrocarbon receptor deficient mice

Open Biol. 2016 Dec;6(12):160186. doi: 10.1098/rsob.160186.

Abstract

Previous studies suggested that the aryl hydrocarbon receptor (AhR) contributes to mice reproduction and fertility. However, the mechanisms involved remain mostly unknown. Retrotransposon silencing by Piwi-interacting RNAs (piRNAs) is essential for germ cell maturation and, remarkably, AhR has been identified as a regulator of murine B1-SINE retrotransposons. Here, using littermate AhR+/+ and AhR-/- mice, we report that AhR regulates the general course of spermatogenesis and oogenesis by a mechanism likely to be associated with piRNA-associated proteins, piRNAs and retrotransposons. piRNA-associated proteins MVH and Miwi are upregulated in leptotene to pachytene spermatocytes with a more precocious timing in AhR-/- than in AhR+/+ testes. piRNAs and transcripts from B1-SINE, LINE-1 and IAP retrotransposons increased at these meiotic stages in AhR-null testes. Moreover, B1-SINE transcripts colocalize with MVH and Miwi in leptonema and pachynema spermatocytes. Unexpectedly, AhR-/- males have increased sperm counts, higher sperm functionality and enhanced fertility than AhR+/+ mice. In contrast, piRNA-associated proteins and B1-SINE and IAP-derived transcripts are reduced in adult AhR-/- ovaries. Accordingly, AhR-null female mice have lower numbers of follicles when compared with AhR+/+ mice. Thus, AhR deficiency differentially affects testis and ovary development possibly by a process involving piRNA-associated proteins, piRNAs and transposable elements.

Keywords: aryl hydrocarbon receptor; fertility; nuage proteins; ovary; repetitive elements; spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Argonaute Proteins / genetics*
  • Argonaute Proteins / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics*
  • DEAD-box RNA Helicases / genetics*
  • DEAD-box RNA Helicases / metabolism
  • Female
  • Fertility
  • Gene Expression Regulation, Developmental
  • Gene Knockout Techniques
  • Male
  • Meiosis
  • Mice
  • Ovary / metabolism*
  • RNA, Small Interfering / metabolism
  • Receptors, Aryl Hydrocarbon / genetics*
  • Retroelements / genetics*
  • Testis / metabolism*
  • Up-Regulation

Substances

  • Ahr protein, mouse
  • Argonaute Proteins
  • Basic Helix-Loop-Helix Transcription Factors
  • Piwil1 protein, mouse
  • RNA, Small Interfering
  • Receptors, Aryl Hydrocarbon
  • Retroelements
  • Ddx4 protein, mouse
  • DEAD-box RNA Helicases