Abstract

During spermatogenesis, the process in which sperm for fertilization are produced from germline cells, gene expression is spatiotemporally highly regulated. In Drosophila, successful expression of extremely large male fertility factor genes on Y-chromosome spanning some megabases due to their gigantic intron sizes is crucial for spermatogenesis. Expression of such extremely large genes must be challenging, but the molecular mechanism that allows it remains unknown. Here we report that a novel RNA-binding protein Maca, which contains two RNA-recognition motifs, is crucial for this process. maca null mutant male flies exhibited a failure in the spermatid individualization process during spermatogenesis, lacked mature sperm, and were completely sterile, while maca mutant female flies were fully fertile. Proteomics and transcriptome analyses revealed that both protein and mRNA abundance of the gigantic male fertility factor genes kl-2, kl-3, and kl-5 (kl genes) are significantly decreased, where the decreases of kl-2 are particularly dramatic, in maca mutant testes. Splicing of the kl-3 transcripts was also dysregulated in maca mutant testes. All these physiological and molecular phenotypes were rescued by a maca transgene in the maca mutant background. Furthermore, we found that in the control genetic background, Maca is exclusively expressed in spermatocytes in testes and enriched at Y-loop A/C in the nucleus, where the kl-5 primary transcripts are localized. Our data suggest that Maca increases transcription processivity, promotes successful splicing of gigantic introns, and/or protects transcripts from premature degradation, of the kl genes. Our study identified a novel RNA-binding protein Maca that is crucial for successful expression of the gigantic male fertility factor genes, spermatogenesis, and male fertility.

Highlights

  • Spermatogenesis is the highly conserved and tightly regulated process where diploid germline stem cells develop into mature, haploid sperm capable of fertilizing oocytes

  • Sperm is produced from germline cells via the process called spermatogenesis, during which a special gene expression program dedicated to this process operates

  • We identified a novel RNA-binding protein encoded in the gene CG5213 that is required for this process

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Summary

Introduction

Spermatogenesis is the highly conserved and tightly regulated process where diploid germline stem cells develop into mature, haploid sperm capable of fertilizing oocytes. Mutations in the germline-specific DAZ (Deleted in AZoospermia) family of RNA-binding proteins, which contain a highly conserved RNA recognition motif (RRM) and are crucial regulators of gene expression during spermatogenesis, impair spermatogenesis and cause human male sterility [1,2,3,4,5,6,7,8,9,10,11,12]. The homologous chromosomes pair and partition into individual chromosome territories, and almost all genes encoding proteins for later meiotic and post-meiotic processes (spermiogenesis) are transcribed. These transcripts are stored without being efficiently translated until their protein activities are required later for meiosis and spermiogenesis. Transcriptional and post-transcriptional events during the spermatocyte growth phase are crucial and must be spatiotemporally highly regulated

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