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      The archetype STYX/dead-phosphatase complexes with a spermatid mRNA-binding protein and is essential for normal sperm production.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Blotting, Northern, Blotting, Western, Carrier Proteins, biosynthesis, genetics, DNA-Binding Proteins, Genetic Vectors, Humans, Male, Mice, Mice, Inbred C57BL, Models, Genetic, Phosphoproteins, Phosphorylation, Plasmids, metabolism, Precipitin Tests, Protein Structure, Tertiary, RNA, RNA Processing, Post-Transcriptional, Spermatogenesis, Spermatozoa, physiology, Testis, Transcription Factors

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          Abstract

          Differentiation of spermatids into spermatozoa is regulated via phosphorylated RNA-binding proteins that modulate the expression of stage-specific mRNAs. We demonstrate that the phosphoserine, -threonine or -tyrosine, interaction protein, Styx, complexes with a testicular RNA-binding protein and is essential for normal spermiogenesis. Ablation of Styx expression in mouse disrupts round and elongating spermatid development, resulting in a >1,000-fold decrease in spermatozoa production. Moreover, Styx(-/-) males are infertile because of structural head abnormalities in residual epididymal sperm. Immunoprecipitation of Styx with Crhsp-24, a phosphorylated RNA-binding protein implicated in translational repression of histone mRNAs, provides a strategy for regulating posttranscriptional gene expression.

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