4.6 Article

Polyubiquitin gene Ubb is required for upregulation of Piwi protein level during mouse testis development

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CELL DEATH DISCOVERY
卷 7, 期 1, 页码 -

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DOI: 10.1038/s41420-021-00581-2

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  1. National University of Singapore (NUS) [20180102]
  2. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2020R1F1A1070847]
  3. National Research Foundation of Korea [2020R1F1A1070847] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Analysis of the testis proteome in Ubb knockout mice revealed 564 proteins significantly differentially expressed, with 36 downregulated proteins involved in various stages of spermatogenesis. Functional gene ontology analysis identified decreased levels of piRNA metabolic process-related proteins, such as Piwil2 and Tdrd1, in Ubb-null testes. Protein-protein interaction mapping showed that 24 testis development-related proteins, including Hsp90aa1, Eef1a1, and Pabpc1, were directly impacted by the depletion of ubiquitin, with mRNA levels of these proteins reduced in Ubb-knockout testes resembling the global downregulation of piRNA-metabolic gene expression at transcriptional and post-transcriptional levels.
Testis development, including early embryonic gonad formation and late postnatal spermatogenesis, is essential for the reproduction of higher metazoans to generate fertile gametes, called sperm. We have previously reported that the polyubiquitin gene Ubb is required for fertility in both male and female mice. In particular, the Ubb-null male mice showed an azoospermia phenotype due to arrest of spermatogenesis at the pachytene stage. Here, we analyzed the whole testis proteome at postnatal day 20 to define the molecular mediators of the male-infertility phenotype caused by Ubb knockout. From the identified proteome, 564 proteins were significantly and differentially expressed in Ubb-knockout testes and, among these, 36 downregulated proteins were involved at different stages of spermatogenesis. We also found that levels of piRNA metabolic process-related proteins, including Piwil2 and Tdrd1, were downregulated in Ubb-null testes through functional gene ontology analysis. Further, protein-protein interaction mapping revealed that 24 testis development-related proteins, including Hsp90aa1, Eef1a1, and Pabpc1, were directly influenced by the depletion of ubiquitin. In addition, the reduced mRNA levels of these proteins were observed in Ubb-knockout testes, which closely resembled the global downregulation of piRNA-metabolic gene expression at the transcriptional and post-transcriptional levels. Together with proteomic and transcriptional analyses, our data suggest that Ubb expression is essential for the maintenance of testicular RNA-binding regulators and piRNA-metabolic proteins to complete spermatogenesis in mice.

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