Systematic variation in mRNA 3′-processing signals during mouse spermatogenesis

Donglin Liu, J. Michael Brockman, Brinda Dass, Lucie N. Hutchins, Priyam Singh, John R. McCarrey, Clinton C. MacDonald, Joel H. Graber

Resultado de la investigación: Articlerevisión exhaustiva

102 Citas (Scopus)

Resumen

Gene expression and processing during mouse male germ cell maturation (spermatogenesis) is highly specialized. Previous reports have suggested that there is a high incidence of alternative 3′-processing in male germ cell mRNAs, including reduced usage of the canonical polyadenylation signal, AAUAAA. We used EST libraries generated from mouse testicular cells to identify 3′-processing sites used at various stages of spermatogenesis (spermatogonia, spermatocytes and round spermatids) and testicular somatic Sertoli cells. We assessed differences in 3′-processing characteristics in the testicular samples, compared to control sets of widely used 3′-processing sites. Using a new method for comparison of degenerate regulatory elements between sequence samples, we identified significant changes in the use of putative 3′-processing regulatory sequence elements in all spermatogenic cell types. In addition, we observed a trend towards truncated 3′-untranslated regions (3′-UTRs), with the most significant differences apparent in round spermatids. In contrast, Sertoli cells displayed a much smaller trend towards 3′-UTR truncation and no significant difference in 3′-processing regulatory sequences. Finally, we identified a number of genes encoding mRNAs that were specifically subject to alternative 3′-processing during meiosis and postmeiotic development. Our results highlight developmental differences in polyadenylation site choice and in the elements that likely control them during spermatogenesis.

Idioma originalEnglish (US)
Páginas (desde-hasta)234-246
Número de páginas13
PublicaciónNucleic acids research
Volumen35
N.º1
DOI
EstadoPublished - ene. 2007
Publicado de forma externa

ASJC Scopus subject areas

  • Genetics

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