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A mouse homologue of the Xenopus germ cell-specific ribonucleic acid/deoxyribonucleic acid-binding proteins p54/p56 interacts with the protamine 2 promoter

Producción científica: Articlerevisión exhaustiva

33 Citas (Scopus)

Resumen

Recent evidence indicates that a member of the Y box-binding family of transcriptional regulators is identical to p56, a predominant protein of messenger ribonucleoprotein complexes. The p56 protein is highly enriched in oocytes and testis, and a functional RNA binding mouse cytoplasmic homologue has been cloned and partially characterized. Because few potential testis- specific transcriptional regulators have been identified, the testis- enriched Y box-binding proteins represent trans-acting elements of a unique model system for the study of haploid gone expression. The 5' flanking region of the testis-specific, haploid-expressed mouse protamine 2 gene contains an element with a 9-of-12 nucleotide identity with the previously defined Y box consensus sequence. We have investigated the possible role of Y box-binding proteins in transcriptional regulation of protamine 2 using specific antibodies and DNA-protein binding assays. Western blot analyses with two different anti-p54/p56 antibodies demonstrate that a mouse homologue of Xenopus p54/p56 is present in transcriptionally active mouse testis nuclear extracts. Our results further indicate that the Xenopus Y box-binding proteins bind to an clement 5' to the mouse protamine 2 gene. Similarly, binding of the mouse testis homologue to the protamine 2 Y box element is demonstrated by gel mobility shift and antibody supershift analyses. The demonstrated interactions between testis-enriched Y box-binding proteins and protamine 2 transcriptional control elements therefore represent a unique system for functional studies to determine the mechanism of regulation of haploid gent expression.

Idioma originalEnglish
Páginas (desde-hasta)524-530
Número de páginas7
PublicaciónBiology of Reproduction
Volumen52
N.º3
DOI
EstadoPublished - 1995

Financiación

FinanciadoresNúmero del financiador
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentR01HD028832

    ASJC Scopus subject areas

    • Reproductive Medicine
    • Cell Biology

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