bioRxivDevelopmental BiologyPreprint
The Rapidly Evolving X-linked miR-506 Family Finetunes Spermatogenesis to Enhance Sperm Competition
Zhuqing WangiD, Yue WangiD, Tong ZhouiD, Sheng CheniD, Dayton MorrisiD, Rubens Daniel Miserani MagalhãesiD, Musheng Li, Shawn WangiD, Hetan Wang, Yeming XieiD, Hayden McSwigginiD, Daniel Oliver, Shuiqiao YuaniD, Huili ZhengiD, Jaaved MohammediD, Eric C. LaiiD, John Robert McCarreyiD, Wei YaniD
Abstract
Despite rapid evolution across eutherian mammals, the X-linked miR-506 family miRNAs are located in a region flanked by two highly conserved protein-coding genes (Slitrk2 and Fmr1) 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-linked miR-506 family 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 the miR-506 family 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-linked miR-506 family 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 the miR-506 family miRNAs function to enhance sperm competitiveness and reproductive fitness of the male by finetuning gene expression during spermatogenesis. Significance StatementThe X-linked miR-506 family 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 the miR-506 family of miRNAs regulates sperm competition and the reproductive fitness of the male.
- organism: mouse
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: benchmarking
- research focus: database / resource
- approach: statistical model
- approach: experimental assay
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Testis-expressed cluster of microRNAs 959-964 controls spermatid differentiation in Drosophila
Sergei Ryazansky, Elena Mikhaleva, … Oxana Olenkina·bioRxiv·Sep 3, 2015
- Male gonad-enriched microRNAs function to control sperm production in C. elegans
Lu Lu, Allison L. Abbott·bioRxiv·Oct 10, 2023
- Complete male-to-female sex reversal in XY mice lacking the miR-17~92 cluster
A. Hurtado, I. Mota-Gomez, … F. J. Barrionuevo·bioRxiv·Mar 22, 2023
- Genomic structure, evolutionary origins, and reproductive function of a large amplified intrinsically disordered protein gene on the X chromosome (Laidx) in mice.
Martin F. Arlt, Michele A. Brogley, … Jacob L. Mueller·G3 Genes Genomes GeneticsPeer-reviewed·Apr 6, 2020
- The molecular evolution of spermatogenesis across mammals
F. Murat, N. Mbengue, … H. Kaessmann·bioRxiv·Nov 8, 2021
- Deficient spermiogenesis in mice lacking Rlim
Feng Wang, Maria G. Gervasi, … Ingolf Bach·eLifePeer-reviewed·Feb 23, 2021