Loss of the importin Kpna2 causes infertility in male mice by disrupting the translocation of testis-specific transcription factors

Karyopherins mediate the movement between the nucleus and cytoplasm of specific proteins in diverse cellular processes. Through a loss-of-function approach, we here examine the role of Karyopherin Subunit Alpha 2 (Kpna2) in spermatogenesis. Knockout male mice exhibited reduced body size and sperm motility, increased sperm abnormalities, and led to the dysregulation of testis gene expression and ultimately to infertility. Impaired mRNA expression mainly affected clusters of genes expressed in spermatids and spermatocytes. Downregulated genes included a set of genes that participate in cell adhesion and extracellular matrix (ECM) organization. We detected both the enrichment of some transcription factors that bind to regions around transcription start sites of downregulated genes and the impaired transport of specific factors to the nucleus of spermatid cells. We propose that Kpna2 is essential in the seminiferous tubules for promoting the translocation of testis-specific transcription factors that control the expression of genes related to ECM organization. [Display omitted] •Kpna2 is essential to produce functional spermatozoa in mice testis•Loss of Kpna2 alters the transcriptional program required for spermatogenesis•Testis transcription factors were enriched around the promoters of downregulated genes•KPNA2 is proposed to control the nuclear import of factors specific to spermatogenesis Molecular biology; Omics; Transcriptomics