The Rapidly Evolving X-linkedmiR-506Family Finetunes Spermatogenesis to Enhance Sperm Competition

  1. Zhuqing Wang
  2. Yue Wang
  3. Tong Zhou
  4. Sheng Chen
  5. Dayton Morris
  6. Rubens Daniel Miserani Magalhães
  7. Musheng Li
  8. Shawn Wang
  9. Hetan Wang
  10. Yeming Xie
  11. Hayden McSwiggin
  12. Daniel Oliver
  13. Shuiqiao Yuan
  14. Huili Zheng
  15. Jaaved Mohammed
  16. Eric C. Lai
  17. John R. McCarrey
  18. Wei Yan
8 evaluations Published on
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Abstract

Despite rapid evolution across eutherian mammals, the X-linkedmiR-506family miRNAs are located in a region flanked by two highly conserved protein-coding genes (Slitrk2andFmr1) on the X chromosome. Intriguingly, these miRNAs are predominantly expressed in the testis, suggesting a potential role in spermatogenesis and male fertility. Here, we report that the X-linkedmiR-506family miRNAs were derived from the MER91C DNA transposons. Selective inactivation of individual miRNAs or clusters caused no discernable defects, but simultaneous ablation of five clusters containing nineteen members of themiR-506family led to reduced male fertility in mice. Despite normal sperm counts, motility and morphology, the KO sperm were less competitive than wild-type sperm when subjected to a polyandrous mating scheme. Transcriptomic and bioinformatic analyses revealed that these X-linkedmiR-506family miRNAs, in addition to targeting a set of conserved genes, have more targets that are critical for spermatogenesis and embryonic development during evolution. Our data suggest that themiR-506family miRNAs function to enhance sperm competitiveness and reproductive fitness of the male by finetuning gene expression during spermatogenesis.

Significance Statement

The X-linkedmiR-506family has rapidly evolved in mammals, but their physiological significance remains elusive. Given their abundant and preferential expression in the testis and sperm, these X-linked miRNAs likely play a functional role in spermatogenesis and/or early embryonic development. However, the deletion of either individual miRNA genes or all of the five miRNA clusters encoding 38 mature miRNAs did not cause major fertility defects in mice. When these mutant males were subjected to conditions resembling polyandrous mating, the mutant sperm were much less competitive than the wild-type sperm, rendering the mutant males “functionally sub-fertile”. Our data suggest that themiR-506family of miRNAs regulates sperm competition and the reproductive fitness of the male.

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