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

导入蛋白 Kpna2 的缺失会破坏睾丸特异性转录因子的易位,从而导致雄性小鼠不育

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作者:Paula Navarrete-López, María Maroto, Eva Pericuesta, Raúl Fernández-González, Marta Lombó, Priscila Ramos-Ibeas, Alfonso Gutiérrez-Adán

Abstract

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.

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